Frontier Integration in Spinal Cord Injury Repair: Engineering-Driven Mechanistic Exploration and a New Paradigm for Clinical Translation

Mi Zhou , Xue Yao , Boya Huang , Jie Ren , Haiwen Feng , Shiqing Feng

Engineering ›› : 202511012

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Engineering ›› :202511012 DOI: 10.1016/j.eng.2025.11.012
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Frontier Integration in Spinal Cord Injury Repair: Engineering-Driven Mechanistic Exploration and a New Paradigm for Clinical Translation
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Abstract

Spinal cord injury (SCI) is a devastating traumatic disorder of the central nervous system that severely impairs sensory, motor, and autonomic functions, placing heavy burdens on patients, families, and society. This review summarizes engineering advances in SCI repair, emphasizing neuromodulation therapies, surgical approaches, cell therapy, pharmacological and gene therapies, and biomaterial-based tissue engineering. It also discusses challenges in clinical translation, such as ethical considerations, multimodal technology integration, and interindividual variability. The review underscores the importance of strengthening interdisciplinary collaboration to integrate multiple-model treatments and accelerate their clinical application.

Keywords

Spinal cord injury / Tissue engineering / Neuromodulation / Biomaterial / Brain-computer interface / Translational medicine

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Mi Zhou, Xue Yao, Boya Huang, Jie Ren, Haiwen Feng, Shiqing Feng. Frontier Integration in Spinal Cord Injury Repair: Engineering-Driven Mechanistic Exploration and a New Paradigm for Clinical Translation. Engineering 202511012 DOI:10.1016/j.eng.2025.11.012

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References

[1]

Wei Y, Xuan A, Lian Y, Wang Z, Xie Y, Yu H. An analysis of the burden of spinal cord injury differences between global epidemiology and trends to America, China and India. Global. Spine J 2025:21925682251370639.

[2]

David G, Mohammadi S, Martin AR, Cohen-Adad J, Weiskopf N, Thompson A, et al. Traumatic and nontraumatic spinal cord injury: pathological insights from neuroimaging. Nat Rev Neurol 2019; 15(12):718-31.

[3]

Lu Y, Shang Z, Zhang W, Pang M, Hu X, Dai Y, et al. Global incidence and characteristics of spinal cord injury since 2000-2021: a systematic review and meta-analysis. BMC Med 2024; 22(1):285.

[4]

Zhou M, Xu Z, Zhong H, Ning G, Feng S. Spinal cord injury and inflammatory mediators: role in “fire barrier” formation and potential for neural regeneration. Neural Regen Res 2026; 21(3):923-37.

[5]

Xing C, Liu S, Wang L, Ma H, Zhou M, Zhong H, et al. Metformin enhances endogenous neural stem cells proliferation, neuronal differentiation, and inhibits ferroptosis through activating AMPK pathway after spinal cord injury. J Transl Med 2024; 22(1):723.

[6]

Zhou M, Xu Z, Feng L, Zhong H, Yang H, Ning G, et al. 50 years of methylprednisolone application in spinal cord injury: a bibliometric analysis. Acta Neurochir 2025; 167(1):38.

[7]

Silva NA, Sousa N, Reis RL, Salgado AJ. From basics to clinical: a comprehensive review on spinal cord injury. Prog Neurobiol 2014;114:25-57.

[8]

Wang R, Bai J. Pharmacological interventions targeting the microcirculation following traumatic spinal cord injury. Neural Regen Res 2024; 19(1):35-42.

[9]

Choo AM, Liu J, Liu Z, Dvorak M, Tetzlaff W, Oxland TR. Modeling spinal cord contusion, dislocation, and distraction: characterization of vertebral clamps, injury severities, and node of Ranvier deformations. J Neurosci Methods 2009; 181(1):6-17.

[10]

Anjum A, Yazid MD, Fauzi Daud M, Idris J, Ng AMH, Selvi Naicker A, et al. Spinal cord injury: pathophysiology, multimolecular interactions, and underlying recovery mechanisms. Int J Mol Sci 2020; 21(20):7533.

[11]

Zhou X, He X, Ren Y. Function of microglia and macrophages in secondary damage after spinal cord injury. Neural Regen Res 2014; 9(20):1787-95.

[12]

Oyinbo CA. Secondary injury mechanisms in traumatic spinal cord injury: a nugget of this multiply cascade. Acta Neurobiol Exp 2011; 71(2):281-99.

[13]

Dimitrijevic MR, Danner SM, Mayr W. Neurocontrol of movement in humans with spinal cord injury. Artif Organs 2015; 39(10):823-33.

[14]

Li J, Zhang Q, Liu Z, Xu W, Fu C, Ding J. Biomaterial-based emergency intervention for secondary spinal cord injury. Small Science. In press.

[15]

Jack A, Rajshekar M, Witiw CD, Curran MWT, Olson JL, Morhart MJ, et al. Characterization of spinal cord injury patients for arm functional restoration through nerve transfer. Can J Neurol Sci 2024; 51(4):477-81.

[16]

Fleming JC, Norenberg MD, Ramsay DA, Dekaban GA, Marcillo AE, Saenz AD, et al. The cellular inflammatory response in human spinal cords after injury. Brain 2006;129(Pt 12):3249-69.

[17]

Shechter R, Schwartz M. CNS sterile injury: just another wound healing? Trends Mol Med 2013; 19(3):135-43.

[18]

Shi Z, Yuan S, Shi L, Li J, Ning G, Kong X, et al. Programmed cell death in spinal cord injury pathogenesis and therapy. Cell Prolif 2021; 54(3):e12992.

[19]

Munteanu C, Rotariu M, Turnea M, Ionescu AM, Popescu C, Spinu A, et al. Main cations and cellular biology of traumatic spinal cord injury. Cells 2022; 11(16):2503.

[20]

Pivoriunas A, Verkhratsky A. Astrocyte-endotheliocyte axis in the regulation of the blood-brain barrier. Neurochem Res 2021; 46(10):2538-50.

[21]

David S, Kroner A. Repertoire of microglial and macrophage responses after spinal cord injury. Nat Rev Neurosci 2011; 12(7):388-99.

[22]

Ye J, Shan F, Xu X, Liang C, Zhang N, Hu H, et al. Centripetal migration and prolonged retention of microglia promotes spinal cord injury repair. J Neuroinflammation 2025; 22(1):77.

[23]

Cutler AJ, Limbani V, Girdlestone J, Navarrete CV. Umbilical cord-derived mesenchymal stromal cells modulate monocyte function to suppress T cell proliferation. J Immunol 2010; 185(11):6617-23.

[24]

Thompson CD, Zurko JC, Hanna BF, Hellenbrand DJ, Hanna A. The therapeutic role of interleukin-10 after spinal cord injury. J Neurotrauma 2013; 30(15):1311-24.

[25]

Dias DO, Göritz C. Fibrotic scarring following lesions to the central nervous system. Matrix Biol 2018;68-69:561-70.

[26]

Zhang Y, Yang S, Liu C, Han X, Gu X, Zhou S. Deciphering glial scar after spinal cord injury. Burns. Trauma 2021;9:tkab035.

[27]

Greenhalgh AD, David S. Differences in the phagocytic response of microglia and peripheral macrophages after spinal cord injury and its effects on cell death. J Neurosci 2014; 34(18):6316-22.

[28]

Rezvan M, Meknatkhah S, Hassannejad Z, Sharif-Alhoseini M, Zadegan SA, Shokraneh F, et al. Time-dependent microglia and macrophages response after traumatic spinal cord injury in rat: a systematic review. Injury 2020; 51(11):2390-401.

[29]

Tran AP, Warren PM, Silver J. The biology of regeneration failure and success after spinal cord injury. Physiol Rev 2018; 98(2):881-917.

[30]

Wiese S, Karus M, Faissner A. Astrocytes as a source for extracellular matrix molecules and cytokines. Front Pharmacol 2012;3:120.

[31]

Ahuja CS, Nori S, Tetreault L, Wilson J, Kwon B, Harrop J, et al. Traumatic spinal cord injury-repair and regeneration. Neurosurgery 2017; 80(3S 3s):S9-S22.

[32]

Richard SA, Sackey M. Elucidating the pivotal neuroimmunomodulation of stem cells in spinal cord injury repair. Stem Cells Int 2021;2021:9230866.

[33]

Hara S, Andresen H, Solheim O, Carlsen SM, Sundstrøm T, Lønne G, et al. Effect of spinal cord burst stimulation vs placebo stimulation on disability in patients with chronic radicular pain after lumbar spine surgery: a randomized clinical trial. J Am Med Assoc 2022; 328(15):1506-14.

[34]

Xu X, Zhou PB. Spinal cord injury caused by electrical stimulation of thoracic spinal cord for treatment of diabetic foot: a case report. J Neurorestoratology 2023; 11(3):100069.

[35]

Zhong H, Xing C, Zhou M, Jia Z, Liu S, Zhu S, et al. Alternating current stimulation promotes neurite outgrowth and plasticity in neurons through activation of the PI3K/AKT signaling pathway. Acta Biochim Biophy Sin 2023; 55(11):1718-29.

[36]

Harkema SJ, Schmidt-Read M, Lorenz DJ, Edgerton VR, Behrman AL. Balance and ambulation improvements in individuals with chronic incomplete spinal cord injury using locomotor training-based rehabilitation. Arch Phys Med Rehabil 2012; 93(9):1508-17.

[37]

Squair JW, Gautier M, Mahe L, Soriano JE, Rowald A, Bichat A, et al. Neuroprosthetic baroreflex controls haemodynamics after spinal cord injury. Nature 2021; 590(7845):308-14.

[38]

Hachmann JT, Grahn PJ, Calvert JS, Drubach DI, Lee KH, Lavrov IA. Electrical neuromodulation of the respiratory system after spinal cord injury. Mayo Clin Proc 2017; 92(9):1401-14.

[39]

Fatima F, Tharu NS, Castillo C, Ng A, Gerasimenko Y, Ovechkin A. Mechanism-based neuromodulation in augmenting respiratory motor function in individuals with spinal cord injury. J Clin Med 2025; 14(11):3827.

[40]

Zhou M, Zhong H, Xing C, Li H, Liu S, Wang L, et al. Comparison of clinical outcomes associated with spinal cord stimulation (SCS) or conventional medical management (CMM) for chronic pain: a systematic review and meta-analysis. Eur Spine J 2023; 32(6):2029-41.

[41]

Chalif JI, Chavarro VS, Mensah E, Johnston B, Fields DP, Chalif EJ, et al. Epidural spinal cord stimulation for spinal cord injury in humans: a systematic review. J Clin Med 2024; 13(4):1090.

[42]

Anderson MA, Squair JW, Gautier M, Hutson TH, Kathe C, Barraud Q, et al. Natural and targeted circuit reorganization after spinal cord injury. Nat Neurosci 2022; 25(12):1584-96.

[43]

Meyer C, Hofstoetter US, Hubli M, Hassani RH, Rinaldo C, Curt A, et al. Immediate effects of transcutaneous spinal cord stimulation on motor function in chronic, sensorimotor incomplete spinal cord injury. J Clin Med 2020; 9(11):3541.

[44]

Zhou K, Wei W, Yang D, Zhang H, Yang W, Zhang Y, et al. Dual electrical stimulation at spinal-muscular interface reconstructs spinal sensorimotor circuits after spinal cord injury. Nat Commun 2024; 15(1):619.

[45]

Liu P, Cheng Y, Xu Z, Li X, Chen Z, Duan W. Spatiotemporal spinal cord stimulation with real-time triggering exoskeleton restores walking capability: a case report. Ann Clin Transl Neurol 2025; 12(3):659-65.

[46]

Hodgkiss DD, Williams AMM, Shackleton CS, Samejima S, Balthazaar SJT, Lam T, et al. Ergogenic effects of spinal cord stimulation on exercise performance following spinal cord injury. Front Neurosci 2024;18:1435716.

[47]

Rowald A, Komi S, Demesmaeker R, Baaklini E, Hernandez-Charpak SD, Paoles E, et al. Activity-dependent spinal cord neuromodulation rapidly restores trunk and leg motor functions after complete paralysis. Nat Med 2022; 28(2):260-71.

[48]

Liu J, Zhang W, Zhou Y, Xu L, Chu YH, Jia F. An open-access lumbosacral spine MRI dataset with enhanced spinal nerve root structure resolution. Sci Data 2024; 11(1):1131.

[49]

Wan KR, Ng ZYV, Wee SK, Fatimah M, Lui W, Phua MW, et al. Recovery of volitional motor control and overground walking in participants with chronic clinically motor complete spinal cord injury: restoration of rehabilitative function with epidural spinal stimulation (restores) trial—a preliminary study. J Neurotrauma 2024; 41(9-10):1146-62.

[50]

Moritz C, Field-Fote EC, Tefertiller C, van Nes I, Trumbower R, Kalsi-Ryan S, et al. Non-invasive spinal cord electrical stimulation for arm and hand function in chronic tetraplegia: a safety and efficacy trial. Nat Med 2024; 30(5):1276-83.

[51]

Angeli CA, Rejc E, Ugiliweneza B, Boakye M, Forrest GF, Brockman K, et al. Activity-based recovery training with spinal cord epidural stimulation improves standing performance in cervical spinal cord injury. J Neuroeng Rehabil 2025; 22(1):101.

[52]

Comino-Suárez N, Moreno JC, Megía-García Á, del-Ama AJ, Serrano-Muñoz D, Avendaño-Coy J, et al. Transcutaneous spinal cord stimulation combined with robotic-assisted body weight-supported treadmill training enhances motor score and gait recovery in incomplete spinal cord injury: a double-blind randomized controlled clinical trial. J Neuroeng Rehabil 2025; 22(1):15.

[53]

Herrity AN, Aslan SC, Mesbah S, Siu R, Kalvakuri K, Ugiliweneza B, et al. Targeting bladder function with network-specific epidural stimulation after chronic spinal cord injury. Sci Rep 2022; 12(1):11179.

[54]

Wagner FB, Mignardot JB, Le Goff-Mignardot CG, Demesmaeker R, Komi S, Capogrosso M, et al. Targeted neurotechnology restores walking in humans with spinal cord injury. Nature 2018; 563(7729):65-71.

[55]

Zhong H, Zhang K, Zhou M, Xing C, An Y, Zhang Q, et al. An implantable self-driven diaphragm pacing system based on a microvibration triboelectric nanogenerator for phrenic nerve stimulation. ACS Appl Mater Interfaces 2024; 16(33):43199-211.

[56]

Wang L, Zhao H, Han M, Yang H, Lei M, Wang W, et al. Electromagnetic cellularized patch with wirelessly electrical stimulation for promoting neuronal differentiation and spinal cord injury repair. Adv Sci 2024; 11(30):e2307527.

[57]

Vallejo R, Chakravarthy K, Will A, Trutnau K, Dinsmoor D. A new direction for closed-loop spinal cord stimulation: combining contemporary therapy paradigms with evoked compound action potential sensing. J Pain Res 2021;14:3909-18.

[58]

Fyfe I. Brain stimulation aids walking after spinal injury. Nat Rev Neurol 2025; 21(2):66.

[59]

Oishi R, Takeda I, Ode Y, Okada Y, Kato D, Nakashima H, et al. Neuromodulation with transcranial direct current stimulation contributes to motor function recovery via microglia in spinal cord injury. Sci Rep 2024; 14(1):18031.

[60]

Huang K, Fang J, Xiao S, Wang W, Zhang G, Sun W, et al. Transcranial alternating current stimulation inhibits ferroptosis and promotes functional recovery in spinal cord injury via the cGMP-PKG signalling pathway. Life Sci 2025;362:123341.

[61]

Zareen N, Dodson S, Armada K, Awad R, Sultana N, Hara E, et al. Stimulation-dependent remodeling of the corticospinal tract requires reactivation of growth-promoting developmental signaling pathways. Exp Neurol 2018;307:133-44.

[62]

Amer A, Martin JH. Repeated motor cortex theta-burst stimulation produces persistent strengthening of corticospinal motor output and durable spinal cord structural changes in the rat. Brain Stimul 2022; 15(4):1013-22.

[63]

Cho N, Squair JW, Aureli V, James ND, Bole-Feysot L, Dewany I, et al. Hypothalamic deep brain stimulation augments walking after spinal cord injury. Nat Med 2024; 30(12):3676-86.

[64]

Tan M, Feng Z, Chen H, Min L, Wen H, Liu H, et al. Transcranial direct current stimulation regulates phenotypic transformation of microglia to relieve neuropathic pain induced by spinal cord injury. Front Behav Neurosci 2023;17:1147693.

[65]

Beisteiner R, Hallett M, Lozano AM. Ultrasound neuromodulation as a new brain therapy. Adv Sci 2023; 10(14):e2205634.

[66]

Xu R, Treeby BE, Martin E. Safety review of therapeutic ultrasound for spinal cord neuromodulation and blood-spinal cord barrier opening. Ultrasound Med Biol 2024; 50(3):317-31.

[67]

Hou L, Lei Y. Spinal cord ultrasound stimulation modulates corticospinal excitability in humans. Brain Stimul 2025; 18(4):1116-30.

[68]

Ahmed RU, Alam M, Li S, Palanisamy P, Zhong H, Zheng YP. A novel therapeutic approach of ultrasound stimulation to restore forelimb functions following cervical cord injury in rats. J Neurorestoratology 2023; 11(3):100067.

[69]

Ning GZ, Song WY, Xu H, Zhu RS, Wu QL, Wu Y, et al. Bone marrow mesenchymal stem cells stimulated with low-intensity pulsed ultrasound: better choice of transplantation treatment for spinal cord injury: treatment for SCI by LIPUS-BMSCs transplantation. CNS Neurosci Ther 2019; 25(4):496-508.

[70]

Liao YH, Tian MH, Zhou WY, He BQ, Tang C, Tang Q, et al. Low-intensity pulsed ultrasound promotes proliferation and differentiation of neural stem cells to enhance spinal cord injury recovery. Mol Biol Rep 2025; 52(1):245.

[71]

Hong Y, Lee E, Park K, Han M, Kim KT, Park J. Ultrasound stimulation improves inflammatory resolution, neuroprotection, and functional recovery after spinal cord injury. Sci Rep 2022; 12(1):3636.

[72]

Zamarioli A, Butezloff MM, Ximenez JPB, Volpon JB. Low-intensity pulsed ultrasound partially reversed the deleterious effects of a severe spinal cord injury-induced bone loss and osteoporotic fracture healing in paraplegic rats. Spinal Cord 2023; 61(2):145-53.

[73]

Weber-Adrian D, Thévenot E, O’Reilly MA, Oakden W, Akens MK, Ellens N, et al. Gene delivery to the spinal cord using MRI-guided focused ultrasound. Gene Ther 2015; 22(7):568-77.

[74]

Payne AH, Hawryluk GW, Anzai Y, Odéen H, Ostlie M, Reichert EC, et al. Magnetic resonance imaging-guided focused ultrasound to increase localized blood-spinal cord barrier permeability. Neural Regen Res 2017; 12(12):2045-9.

[75]

Song Z, Ye Y, Zhang Z, Shen J, Hu Z, Wang Z, et al. Noninvasive, targeted gene therapy for acute spinal cord injury using LIFU-mediated BDNF-loaded cationic nanobubble destruction. Biochem Biophys Res Commun 2018; 496(3):911-20.

[76]

Song Z, Wang Z, Shen J, Xu S, Hu Z. Nerve growth factor delivery by ultrasound-mediated nanobubble destruction as a treatment for acute spinal cord injury in rats. Int J Nanomed 2017;12:1717-29.

[77]

Blackmore J, Shrivastava S, Sallet J, Butler CR, Cleveland RO. Ultrasound neuromodulation: a review of results, mechanisms and safety. Ultrasound Med Biol 2019; 45(7):1509-36.

[78]

Chou YH, Sundman M, Ton That V, Green J, Trapani C. Cortical excitability and plasticity in Alzheimer’s disease and mild cognitive impairment: a systematic review and meta-analysis of transcranial magnetic stimulation studies. Ageing Res Rev 2022;79:101660.

[79]

Arora T, Desai N, Kirshblum S, Chen R. Utility of transcranial magnetic stimulation in the assessment of spinal cord injury: current status and future directions. Front Rehabil Sci 2022;3:1005111.

[80]

Jung J, Patel S, Khan A, Baamonde AD, Mirallave-Pescador A, Chowdhury YA, et al. nTMS in spinal cord injury: current evidence, challenges and a future direction. Brain Spine 2025;5:104234.

[81]

Aberra AS, Wang B, Grill WM, Peterchev AV. Simulation of transcranial magnetic stimulation in head model with morphologically-realistic cortical neurons. Brain Stimul 2020; 13(1):175-89.

[82]

Yang HY, Liu Y, Xie JC, Liu NN, Tian X. Effects of repetitive transcranial magnetic stimulation on synaptic plasticity and apoptosis in vascular dementia rats. Behav Brain Res 2015;281:149-55.

[83]

Kim HM, Jo HS, Kim EJ, Na JM, Park HK, Han JY, et al. The effect of repetitive transcranial magnetic stimulation on cognition in diffuse axonal injury in a rat model. Neurol Int 2024; 16(4):689-700.

[84]

Zhang Y, Zhang Y, Chen Z, Ren P, Fu Y. Continuous high-frequency repetitive transcranial magnetic stimulation at extremely low intensity affects exploratory behavior and spatial cognition in mice. Behav Brain Res 2024;458:114739.

[85]

Caparelli EC, Abulseoud OA, Gu H, Zhai T, Schleyer B, Yang Y. Low frequency repetitive transcranial magnetic stimulation to the right dorsolateral prefrontal cortex engages thalamus, striatum, and the default mode network. Front Neurosci 2022;16:997259.

[86]

Benito J, Kumru H, Murillo N, Costa U, Medina J, Tormos J, et al. Motor and gait improvement in patients with incomplete spinal cord injury induced by high-frequency repetitive transcranial magnetic stimulation. Top Spinal Cord Inj Rehabil 2012; 18(2):106-12.

[87]

Nogueira F, Shirahige L, Brito R, Lima H, Victor J, Sanchez MP, et al. Repetitive transcranial magnetic stimulation with body weight-supported treadmill training enhances independent walking of individuals with chronic incomplete spinal cord injury: a pilot randomized clinical trial. Brain Topogr 2024; 37(6):1232-41.

[88]

Wang P, Yin R, Wang S, Zhou T, Zhang Y, Xiao M, et al. Effects of repetitive transcranial magnetic stimulation (RTMS) and treadmill training on recovery of motor function in a rat model of partial spinal cord injury. Med Sci Monit 2021;27:e931601.

[89]

Zhang L, Xiao Z, Su Z, Wang X, Tian H, Su M. Repetitive transcranial magnetic stimulation promotes motor function recovery in mice after spinal cord injury via regulation of the Cx43-autophagy loop. J Orthop Surg Res 2024; 19(1):387.

[90]

Berlowitz DJ, Wadsworth B, Ross J. Respiratory problems and management in people with spinal cord injury. Breathe 2016;12(4):328-40.

[91]

Farahani M, Gnatowski P, Najafloo R, Navaei T, Piłat E, Kucińska-Lipka J, et al. Enhancing diaphragmatic defect repair and regeneration: how biomaterials leading the way to progress? BMEmat 2024; 2(3):e12070.

[92]

Lee KZ, Liou LM, Vinit S, Ren MY. Rostral-caudal effect of cervical magnetic stimulation on the diaphragm motor evoked potential after cervical spinal cord contusion in the rat. J Neurotrauma 2022; 39(9-10):683-700.

[93]

Yang N, Xiao Q, Liu T, Zhang F. Early repetitive transcranial magnetic stimulation in the spinal cord region for the treatment of spinal cord injury: a case report. Medicine 2025; 104(25):e42948.

[94]

Lin BS, Zhang Z, Peng CW, Chen SH, Chan WP, Lai CH. Effectiveness of repetitive transcranial magnetic stimulation combined with transspinal electrical stimulation on corticospinal excitability for individuals with incomplete spinal cord injury: a pilot study. IEEE Trans Neural Syst Rehabil Eng 2023;31:4790-800.

[95]

Ramezani F, Razmgir M, Tanha K, Nasirinezhad F, Neshastehriz A, Bahrami-Ahmadi A, et al. Photobiomodulation for spinal cord injury: a systematic review and meta-analysis. Physiol Behav 2020;224:112977.

[96]

Neshasteh-Riz A, Ramezani F, Kookli K, Moghaddas Fazeli S, Motamed A, Nasirinezhad F, et al. Optimization of the duration and dose of photobiomodulation therapy (660 nm laser) for spinal cord injury in rats. Photobiomodul Photomed Laser Surg 2022; 40(7):488-98.

[97]

Byrnes KR, Waynant RW, Ilev IK, Wu X, Barna L, Smith K, et al. Light promotes regeneration and functional recovery and alters the immune response after spinal cord injury. Lasers Surg Med 2005; 36(3):171-85.

[98]

Song JW, Li K, Liang ZW, Dai C, Shen XF, Gong YZ, et al. Low-level laser facilitates alternatively activated macrophage/microglia polarization and promotes functional recovery after crush spinal cord injury in rats. Sci Rep 2017; 7(1):620.

[99]

Zhu Z, Wang X, Song Z, Zuo X, Ma Y, Zhang Z, et al. Photobiomodulation promotes repair following spinal cord injury by restoring neuronal mitochondrial bioenergetics via AMPK/PGC-1 a /TFAM pathway. Front Pharmacol 2022;13:991421.

[100]

Ju C, Ma Y, Zuo X, Wang X, Song Z, Zhang Z, et al. Potential targets and mechanisms of photobiomodulation for spinal cord injury. Neural Regen Res 2023; 18(8):1782-2178.

[101]

Stevens AR, Hadis M, Alldrit H, Milward MR, Di Pietro V, Gendoo DMA, et al. Evaluation of transcriptomic changes after photobiomodulation in spinal cord injury. Sci Rep 2025; 15(1):3193.

[102]

Zhang Z, Zhu Z, Zuo X, Wang X, Ju C, Liang Z, et al. Photobiomodulation reduces neuropathic pain after spinal cord injury by downregulating CXCL10 expression. CNS Neurosci Ther 2023; 29(12):3995-4017.

[103]

da Silva FC, Silva T, Gomes AO, da Costa Palácio PR, Andreo L, Gonçalves MLL, et al. Sensory and motor responses after photobiomodulation associated with physiotherapy in patients with incomplete spinal cord injury: clinical, randomized trial. Lasers Med Sci 2020; 35(8):1751-8.

[104]

Liang Z, Lei T, Wang S, Li P, Chen B, Pan D, et al. Clinical safety study of photobiomodulation in acute spinal cord injury by scattering fiber. Lasers Med Sci 2022; 37(9):3433-42.

[105]

Joshi J, Rubart M, Zhu W. Optogenetics: background, methodological advances and potential applications for cardiovascular research and medicine. Front Bioeng Biotechnol 2020;7:466.

[106]

Ma YH, Chen HY, Wei QS, Peng LZ, Zhang KJ, Deng QW, et al. Transcranial optogenetic stimulation promotes corticospinal tract axon regeneration to repair spinal cord injury by activating the JAK2/STAT3 pathway. Neurospine 2025; 22(2):311-28.

[107]

Mondello SE, Young L, Dang V, Fischedick AE, Tolley NM, Wang T, et al. Optogenetic spinal stimulation promotes new axonal growth and skilled forelimb recovery in rats with sub-chronic cervical spinal cord injury. J Neural Eng 2023; 20(5):056005.

[108]

Deng W, Wu G, Min L, Feng Z, Chen H, Tan M, et al. Optogenetic neuronal stimulation promotes functional recovery after spinal cord injury. Front Neurosci 2021;15:640255.

[109]

Sun Y, Chen X, Gao X. The potential of diverse brain-computer interface signal acquisition techniques in neurorestoratology. J Neurorestoratology 2024; 12(3):100138.

[110]

Pichiorri F, Morone G, Petti M, Toppi J, Pisotta I, Molinari M, et al. Brain-computer interface boosts motor imagery practice during stroke recovery. Ann Neurol 2015; 77(5):851-65.

[111]

Wang A, Tian X, Jiang D, Yang C, Xu Q, Zhang Y, et al. Rehabilitation with brain-computer interface and upper limb motor function in ischemic stroke: a randomized controlled trial. Med 2024; 5(6):559-569.e4.

[112]

Vansteensel MJ, Leinders S, Branco MP, Crone NE, Denison T, Freudenburg ZV, et al. Longevity of a brain-computer interface for amyotrophic lateral sclerosis. N Engl J Med 2024; 391(7):619-26.

[113]

Köhler RM, Binns TS, Merk T, Zhu G, Yin Z, Zhao B, et al. Dopamine and deep brain stimulation accelerate the neural dynamics of volitional action in Parkinson’s disease. Brain 2024; 147(10):3358-69.

[114]

Liberati G, da Rocha JLD, van der Heiden L, Raffone A, Birbaumer N, Olivetti Belardinelli M, et al. Toward a brain-computer interface for Alzheimer’s disease patients by combining classical conditioning and brain state classification. J Alzheimers Dis 2012; 31(Suppl 3):S211-20.

[115]

Fu Y, Xue Y, Chen X, Hu Y. Brain-computer interface (BCI) in clinical neurorestorative practices. J Neurorestoratology 2025; 13(2):100188.

[116]

He G, Dong X, Qi M. From the perspective of material science: a review of flexible electrodes for brain-computer interface. Mater Res Express 2020; 7(10):102001.

[117]

Fu Y, Chen X, Hu Y. Correct understanding of brain-computer interfaces. J Neurorestoratology 2024; 12(3):100139.

[118]

Lazarou I, Nikolopoulos S, Petrantonakis PC, Kompatsiaris I, Tsolaki M. EEG-based brain-computer interfaces for communication and rehabilitation of people with motor impairment: a novel approach of the 21st Century. Front Hum Neurosci 2018;12:14.

[119]

Cope AP, Jasenecova M, Vasconcelos JC, Filer A, Raza K, Qureshi S, et al. Abatacept in individuals at high risk of rheumatoid arthritis (APIPPRA): a randomised, double-blind, multicentre, parallel, placebo-controlled, phase 2b clinical trial. Lancet 2024; 403(10429):838-49.

[120]

Dubey A, Ray S. Cortical electrocorticogram (ECoG) is a local signal. J Neurosci 2019; 39(22):4299-311.

[121]

Kanth ST, Ray S. Electrocorticogram (ECoG) is highly informative in primate visual cortex. J Neurosci 2020; 40(12):2430-44.

[122]

Du B, Cheng X, Duan Y, Ning H. fMRI brain decoding and its applications in brain-computer interface: a survey. Brain Sci 2022; 12(2):228.

[123]

Lorach H, Galvez A, Spagnolo V, Martel F, Karakas S, Intering N, et al. Walking naturally after spinal cord injury using a brain-spine interface. Nature 2023; 618(7963):126-33.

[124]

Kumari R, Dybus A, Purcell M, Vučković A. Motor priming to enhance the effect of physical therapy in people with spinal cord injury. J Spinal Cord Med 2025; 48(2):312-26.

[125]

Ajiboye AB, Willett FR, Young DR, Memberg WD, Murphy BA, Miller JP, et al. Restoration of reaching and grasping movements through brain-controlled muscle stimulation in a person with tetraplegia: a proof-of-concept demonstration. Lancet 2017; 389(10081):1821-30.

[126]

Cajigas I, Davis KC, Prins NW, Gallo S, Naeem JA, Fisher L, et al. Brain-computer interface control of stepping from invasive electrocorticography upper-limb motor imagery in a patient with quadriplegia. Front Hum Neurosci 2022;16:1077416.

[127]

Willsey MS, Shah NP, Avansino DT, Hahn NV, Jamiolkowski RM, Kamdar FB, et al. A high-performance brain-computer interface for finger decoding and quadcopter game control in an individual with paralysis. Nat Med 2025; 31(1):96-104.

[128]

Oliveira DS, Ponfick M, Braun DI, Osswald M, Sierotowicz M, Chatterjee S, et al. A direct spinal cord-computer interface enables the control of the paralysed hand in spinal cord injury. Brain 2024; 147(10):3583-95.

[129]

Levett JJ, Elkaim LM, Niazi F, Weber MH, Iorio-Morin C, Bonizzato M, et al. Invasive brain computer interface for motor restoration in spinal cord injury: a systematic review. Neuromodulation 2024; 27(4):597-603.

[130]

Nas K, Yazmalar LS, ah V, Aydın A, Önes K. Rehabilitation of spinal cord injuries. World J Orthop 2015; 6(1):8-16.

[131]

Scalise M, Bora TS, Zancanella C, Safa A, Stefini R, Cannizzaro D. Virtual reality as a therapeutic tool in spinal cord injury rehabilitation: a comprehensive evaluation and systematic review. J Clin Med 2024; 13(18):5429.

[132]

Schultz KR, Mona LR, Cameron RP. Mental health and spinal cord injury: clinical considerations for rehabilitation providers. Curr Phys Med Rehabil Rep 2022; 10(3):131-9.

[133]

Pelletier C. Exercise prescription for persons with spinal cord injury: a review of physiological considerations and evidence-based guidelines. Appl Physiol Nutr Metab 2023; 48(12):882-95.

[134]

Nepomuceno P, Souza WH, Pakosh M, Musselman KE, Craven BC. Exoskeleton-based exercises for overground gait and balance rehabilitation in spinal cord injury: a systematic review of dose and dosage parameters. J Neuroeng Rehabil 2024; 21(1):73.

[135]

Spungen AM, Dematt EJ, Biswas K, Jones KM, Mi Z, Snodgrass AJ, et al. Exoskeletal-assisted walking in veterans with paralysis: a randomized clinical trial. JAMA Netw Open 2024; 7(9):e2431501.

[136]

McKenzie K, Veit N, Aalla S, Yang C, Giffhorn M, Lynott A, et al. Combining neuromodulation strategies in spinal cord injury gait rehabilitation: a proof of concept, randomized, crossover trial. Arch Phys Med Rehabil 2024; 105(10):1930-7.

[137]

Tsai CY, Weinrauch WJ, Manente N, Huang V, Bryce TN, Spungen AM. Exoskeletal-assisted walking during acute inpatient rehabilitation enhances recovery for persons with spinal cord injury—a pilot randomized controlled trial. J Neurotrauma 2024; 41(17-18):2089-100.

[138]

Sandarage R, Nashed JY, Tsai EC. Time is spine: critical updates for the intensivist. Curr Opin Crit Care 2025; 31(2):117-22.

[139]

Zhang B, Jin Z, Luo P, Yin H, Chen X, Yang B, et al. Ischemia-reperfusion injury after spinal cord decompressive surgery—an in vivo rat model. Animal Model Exp Med 2025; 8(3):405-20.

[140]

Chen G, Lin C, Zhu Z, Tong K, Li S, Chen H, et al. Increased blood flow of spinal cord lesion after decompression improves neurological recovery of degenerative cervical myelopathy: an intraoperative ultrasonography-based prospective cohort study. Int J Surg 2023; 109(5):1149-57.

[141]

Quddusi A, Pedro KM, Alvi MA, Hejrati N, Fehlings MG. Early surgical intervention for acute spinal cord injury: time is spine. Acta Neurochir 2023; 165(9):2665-74.

[142]

Badhiwala JH, Wilson JR, Witiw CD, Harrop JS, Vaccaro AR, Aarabi B, et al. The influence of timing of surgical decompression for acute spinal cord injury: a pooled analysis of individual patient data. Lancet Neurol 2021; 20(2):117-26.

[143]

Badhiwala JH, Wilson JR, Harrop JS, Vaccaro AR, Aarabi B, Geisler FH, et al. Early vs late surgical decompression for central cord syndrome. JAMA Surg 2022; 157(11):1024-32.

[144]

Chryssikos T, Stokum JA, Ahmed AK, Chen C, Wessell A, Cannarsa G, et al. Surgical decompression of traumatic cervical spinal cord injury: a pilot study comparing real-time intraoperative ultrasound after laminectomy with postoperative MRI and CT myelography. Neurosurgery 2023; 92(2):353-62.

[145]

Kwon BK, Tetreault LA, Evaniew N, Skelly AC, Fehlings MG. Ao spine/praxis clinical practice guidelines for the management of acute spinal cord injury: an introduction to a focus issue. Global Spine J 2024; 14(3 suppl):5s-9s.

[146]

Squair JW, Bélanger LM, Tsang A, Ritchie L, Mac-Thiong JM, Parent S, et al. Spinal cord perfusion pressure predicts neurologic recovery in acute spinal cord injury. Neurology 2017; 89(16):1660-7.

[147]

Werndle MC, Saadoun S, Phang I, Czosnyka M, Varsos GV, Czosnyka ZH, et al. Monitoring of spinal cord perfusion pressure in acute spinal cord injury: initial findings of the injured spinal cord pressure evaluation study. Crit Care Med 2014; 42(3):646-55.

[148]

Ranjan AK, Gulati A. Controls of central and peripheral blood pressure and hemorrhagic/hypovolemic shock. J Clin Med 2023; 12(3):1108.

[149]

Hawryluk G, Whetstone W, Saigal R, Ferguson A, Talbott J, Bresnahan J, et al. Mean arterial blood pressure correlates with neurological recovery after human spinal cord injury: analysis of high frequency physiologic data. J Neurotrauma 2015; 32(24):1958-67.

[150]

Weinberg JA, Farber SH, Kalamchi LD, Brigeman ST, Bohl MA, Varda BM, et al. Mean arterial pressure maintenance following spinal cord injury: does meeting the target matter? J Trauma Acute Care Surg 2021; 90(1):97-106.

[151]

Catapano JS, Hawryluk GWJ, Whetstone W, Saigal R, Ferguson A, Talbott J, et al. Higher mean arterial pressure values correlate with neurologic improvement in patients with initially complete spinal cord injuries. World Neurosurg 2016;96:72-9.

[152]

Hamers FP, Lankhorst AJ, van Laar TJ, Veldhuis WB, Gispen WH. Automated quantitative gait analysis during overground locomotion in the rat: its application to spinal cord contusion and transection injuries. J Neurotrauma 2001; 18(2):187-201.

[153]

Saadoun S, Asif H, Papadopoulos MC. The concepts of intra spinal pressure (ISP), intra thecal pressure (ITP), and spinal cord perfusion pressure (SCPP) in acute, severe traumatic spinal cord injury: narrative review. Brain Spine 2024;4:103919.

[154]

Ene CI, Wang AC, Collins KL, Bonow RH, McGrath LB, Durfy SJ, et al. Expansile duraplasty and obex exploration compared with bone-only decompression for Chiari malformation type I in children: retrospective review of outcomes and complications. J Neurosurg Pediatr 2021; 27(1):1-8.

[155]

Robinson E, Saigal R, Greil M. 194. Expansile duraplasty improves motor outcomes after acute traumatic spinal cord injury. Spine J 2022; 22(9 Supplement):S102-3.

[156]

Telemacque D, Zhu F-Z, Ren Z-W, Chen K-F, Drepaul D, Yao S, et al. Effects of durotomy versus myelotomy in the repair of spinal cord injury. Neural Regen Res 2020; 15(10):1814-20.

[157]

Saadoun S, Grassner L, Belci M, Cook J, Knight R, Davies L, et al. Duroplasty for injured cervical spinal cord with uncontrolled swelling: protocol of the DISCUS randomized controlled trial. Trials 2023; 24(1):497.

[158]

Dam-Hieu P, Liu S, Tadié M. Experimental bypass surgery between the spinal cord and caudal nerve roots for spinal cord injuries. Neurochirurgie 2004; 50(5):500-14.

[159]

Dam-Hieu P, Liu S, Choudhri T, Said G, Tadié M. Regeneration of primary sensory axons into the adult rat spinal cord via a peripheral nerve graft bridging the lumbar dorsal roots to the dorsal column. J Neurosci Res 2002; 68(3):293-304.

[160]

Hsueh YH, Li YW, Chen KP, Chen WL, Tu YK. Nerve bypass surgery for spinal cord reconstruction. World Neurosurg 2024;189:e27-37.

[161]

Xiang YT, Wu JJ, Ma J, Xing XX, Zhang JP, Hua XY, et al. Peripheral nerve transfers for dysfunctions in central nervous system injuries: a systematic review. Int J Surg 2024; 110(6):3814-26.

[162]

Berger MJ, Dengler J, Westman A, Curt A, Schubert M, Abel R, et al. Nerve transfer after cervical spinal cord injury: who has a “time sensitive” injury based on electrodiagnostic findings? Arch Phys Med Rehabil 2024; 105(4):682-9.

[163]

Olivi S, Paglierani P, Maietti E, Rucci P, Musumeci G, Kiekens C, et al. Nerve transfer for upper extremity reanimation in people with spinal cord injury: a 2-year follow-up case series. J Spinal Cord Med 2025; 48(3):395-404.

[164]

Assinck P, Duncan GJ, Hilton BJ, Plemel JR, Tetzlaff W. Cell transplantation therapy for spinal cord injury. Nat Neurosci 2017; 20(5):637-47.

[165]

Li S, Tang H, Li C, Ma J, Ali M, Dong Q, et al. Synthetic biology technologies and genetically engineering strategies for enhanced cell therapeutics. Stem Cell Rev Rep 2023; 19(2):309-21.

[166]

Fan B, Wei Z, Feng S. Progression in translational research on spinal cord injury based on microenvironment imbalance. Bone Res 2022; 10(1):35.

[167]

Zhang J, Zheng X, Wu Z, Wang Y, Chen H. Neural stem/progenitor cell transplantation therapy for chronic spinal cord injury. J Neurorestoratology 2025; 13(5):100223.

[168]

Li M, Jiang Y, Hou Q, Zhao Y, Zhong L, Fu X. Potential pre-activation strategies for improving therapeutic efficacy of mesenchymal stem cells: current status and future prospects. Stem Cell Res Ther 2022; 13(1):146.

[169]

Curtis E, Martin JR, Gabel B, Sidhu N, Rzesiewicz TK, Mandeville R, et al. A first-in-human, phase I study of neural stem cell transplantation for chronic spinal cord injury. Cell Stem Cell 2018; 22(6):941-950.e6.

[170]

Martin JR, Cleary D, Abraham ME, Mendoza M, Cabrera B, Jamieson C, et al. Long-term clinical and safety outcomes from a single-site phase 1 study of neural stem cell transplantation for chronic thoracic spinal cord injury. Cell Rep Med 2024; 5(12):101841.

[171]

Bydon M, Qu W, Moinuddin FM, Hunt CL, Garlanger KL, Reeves RK, et al. Intrathecal delivery of adipose-derived mesenchymal stem cells in traumatic spinal cord injury: phase I trial. Nat Commun 2024; 15(1):2201.

[172]

Akhlaghpasand M, Tavanaei R, Hosseinpoor M, Heidari R, Mohammadi I, Chamanara M, et al. Effects of combined intrathecal mesenchymal stem cells and Schwann cells transplantation on neuropathic pain in complete spinal cord injury: a phase II randomized active-controlled trial. Cell Transplant 2025;34:09636897241298128.

[173]

Honmou O, Yamashita T, Morita T, Oshigiri T, Hirota R, Iyama S, et al. Intravenous infusion of auto serum-expanded autologous mesenchymal stem cells in spinal cord injury patients: 13 case series. Clin Neurol Neurosurg 2021;203:106565.

[174]

Kaplan N, Kabatas S, Civelek E, Savrunlu EC, Akkoc T, Boyalı O, et al. Multiroute administration of Wharton’s jelly mesenchymal stem cells in chronic complete spinal cord injury: a phase I safety and feasibility study. World J Stem Cells 2025; 17(5):101675.

[175]

Smirnov VA, Radaev SM, Morozova YV, Ryabov SI, Yadgarov MY, Bazanovich SA, et al. Systemic administration of allogeneic cord blood mononuclear cells in adults with severe acute contusion spinal cord injury: phase 1/2a pilot clinical study-safety and primary efficacy evaluation. World Neurosurg 2022;161:e319-38.

[176]

Saini R, Pahwa B, Agrawal D, Singh PK, Gujjar H, Mishra S, et al. Efficacy and outcome of bone marrow derived stem cells transplanted via intramedullary route in acute complete spinal cord injury—a randomized placebo controlled trial. J Clin Neurosci 2022;100:7-14.

[177]

Akhlaghpasand M, Tavanaei R, Allameh F, Hosseinpoor M, Toreyhi H, Golmohammadi M, et al. Improvement of neurogenic bladder dysfunction following combined cell therapy with mesenchymal stem cell and schwann cell in spinal cord injury: a randomized, open-label, phase II clinical trial. World Neurosurg 2024;194:123402.

[178]

Albu S, Kumru H, Coll R, Vives J, Vallés M, Benito-Penalva J, et al. Clinical effects of intrathecal administration of expanded Wharton jelly mesenchymal stromal cells in patients with chronic complete spinal cord injury: a randomized controlled study. Cytotherapy 2021; 23(2):146-56.

[179]

Gant KL, Guest JD, Palermo AE, Vedantam A, Jimsheleishvili G, Bunge MB, et al. Phase 1 safety trial of autologous human Schwann cell transplantation in chronic spinal cord injury. J Neurotrauma 2022; 39(3-4):285-99.

[180]

Koda M, Imagama S, Nakashima H, Ito S, Segi N, Ouchida J, et al. Safety and feasibility of intravenous administration of a single dose of allogenic-Muse cells to treat human cervical traumatic spinal cord injury: a clinical trial. Stem Cell Res Ther 2024; 15(1):259.

[181]

Asano T, Ageyama N, Takeuchi K, Momoeda M, Kitano Y, Sasaki K, et al. Engraftment and tumor formation after allogeneic in utero transplantation of primate embryonic stem cells. Transplantation 2003; 76(7):1061-7.

[182]

Kim DH, Cho HJ, Park CY, Cho MS, Kim DW. Transplantation of PSA-NCAM-positive neural precursors from human embryonic stem cells promotes functional recovery in an animal model of spinal cord injury. Tissue Eng Regen Med 2022; 19(6):1349-58.

[183]

Jones I, Novikova LN, Wiberg M, Carlsson L, Novikov LN. Human embryonic stem cell-derived neural crest cells promote sprouting and motor recovery following spinal cord injury in adult rats. Cell Transplant 2021;30:963689720988245.

[184]

Aboul-Soud MAM, Alzahrani AJ, Mahmoud A. Induced pluripotent stem cells (iPSCs)-roles in regenerative therapies, disease modelling and drug screening. Cells 2021; 10(9):2319.

[185]

Gong C, Zheng X, Guo FL, Wang YN, Zhang S, Chen J, et al. Human spinal GABA neurons alleviate spasticity and improve locomotion in rats with spinal cord injury. Cell Rep 2021; 34(12):108889.

[186]

Wertheim L, Edri R, Goldshmit Y, Kagan T, Noor N, Ruban A, et al. Regenerating the injured spinal cord at the chronic phase by engineered iPSCs-derived 3D neuronal networks. Adv Sci 2022; 9(11):e2105694.

[187]

Wu Z, Zhou Y, Hou X, Liu W, Yin W, Wang L, et al. Construction of functional neural network tissue combining CBD-NT3-modified linear-ordered collagen scaffold and TrkC-modified iPSC-derived neural stem cells for spinal cord injury repair. Bioact Mater 2024;35:242-58.

[188]

Li X, Fan C, Xiao Z, Zhao Y, Zhang H, Sun J, et al. A collagen microchannel scaffold carrying paclitaxel-liposomes induces neuronal differentiation of neural stem cells through Wnt/ b -catenin signaling for spinal cord injury repair. Biomaterials 2018;183:114-27.

[189]

Zhao H, Xiong T, Chu Y, Hao W, Zhao T, Sun X, et al. Biomimetic dual-network collagen fibers with porous and mechanical cues reconstruct neural stem cell niche via AKT/YAP mechanotransduction after spinal cord injury. Small 2024; 20(32):2311456.

[190]

Sabelström H, Stenudd M, Réu P, Dias DO, Elfineh M, Zdunek S, et al. Resident neural stem cells restrict tissue damage and neuronal loss after spinal cord injury in mice. Science 2013; 342(6158):637-40.

[191]

Tai W, Wu W, Wang LL, Ni H, Chen C, Yang J, et al. In vivo reprogramming of NG2 glia enables adult neurogenesis and functional recovery following spinal cord injury. Cell Stem Cell 2021; 28(5):923-937.e4.

[192]

Liu X, Hao M, Chen Z, Zhang T, Huang J, Dai J, et al. 3D bioprinted neural tissue constructs for spinal cord injury repair. Biomaterials 2021;272:120771.

[193]

Lai BQ, Wu RJ, Han WT, Bai YR, Liu JL, Yu HY, et al. Tail nerve electrical stimulation promoted the efficiency of transplanted spinal cord-like tissue as a neuronal relay to repair the motor function of rats with transected spinal cord injury. Biomaterials 2023;297:122103.

[194]

Wang J, Jiang P, Deng W, Sun Y, Liu Y. Grafted human ESC-derived astroglia repair spinal cord injury via activation of host anti-inflammatory microglia in the lesion area. Theranostics 2022; 12(9):4288-309.

[195]

Yoo D, Jung SY, Go D, Park JY, You DG, Jung WK, et al. Functionalized extracellular vesicles of mesenchymal stem cells for regenerative medicine. J Nanobiotechnology 2025; 23(1):219.

[196]

Cho SR, Kim YR, Kang HS, Yim SH, Park C, Min YH, et al. Functional recovery after the transplantation of neurally differentiated mesenchymal stem cells derived from bone marrow in a rat model of spinal cord injury. Cell Transplant 2009; 18(12):1359-68.

[197]

Luo H, Xu C, Liu Z, Yang L, Hong Y, Liu G, et al. Neural differentiation of bone marrow mesenchymal stem cells with human brain-derived neurotrophic factor gene-modified in functionalized self-assembling peptide hydrogel in vitro. J Cell Biochem 2019; 120(3):2828-35.

[198]

Liu W, Ma Z, Li J, Kang X. Mesenchymal stem cell-derived exosomes: therapeutic opportunities and challenges for spinal cord injury. Stem Cell Res Ther 2021; 12(1):102.

[199]

Lim M, Wang W, Liang L, Han Z, Li Z, Geng J, et al. Intravenous injection of allogeneic umbilical cord-derived multipotent mesenchymal stromal cells reduces the infarct area and ameliorates cardiac function in a porcine model of acute myocardial infarction. Stem Cell Res Ther 2018; 9(1):129.

[200]

Yang L, Cao J, Du Y, Zhang X, Hong W, Peng B, et al. Initial IL-10 production dominates the therapy of mesenchymal stem cell scaffold in spinal cord injury. Theranostics 2024; 14(2):879-91.

[201]

Liang Z, Yang Z, Xie H, Rao J, Xu X, Lin Y, et al. Small extracellular vesicles from hypoxia-preconditioned bone marrow mesenchymal stem cells attenuate spinal cord injury via miR-146a-5p-mediated regulation of macrophage polarization. Neural Regen Res 2024; 19(10):2259-69.

[202]

Ursavas S, Darici H, Karaoz E. Olfactory ensheathing cells: unique glial cells promising for treatments of spinal cord injury. J Neurosci Res 2021; 99(6):1579-97.

[203]

Zhang L, Zhuang X, Kotitalo P, Keller T, Krzyczmonik A, Haaparanta-Solin M, et al. Intravenous transplantation of olfactory ensheathing cells reduces neuroinflammation after spinal cord injury via interleukin-1 receptor antagonist. Theranostics 2021; 11(3):1147-61.

[204]

Jiang C, Chen Z, Wang X, Zhang Y, Guo X, Fan H, et al. Curcumin-activated olfactory ensheathing cells improve functional recovery after spinal cord injury by modulating microglia polarization through APOE/TREM2/NF- j B signaling pathway. J Neuroimmune Pharmacol 2023; 18(3):476-94.

[205]

Gaudet AD, Fonken LK. Glial cells shape pathology and repair after spinal cord injury. Neurotherapeutics 2018; 15(3):554-77.

[206]

Marquardt LM, Doulames VM, Wang AT, Dubbin K, Suhar RA, Kratochvil MJ, et al. Designer, injectable gels to prevent transplanted Schwann cell loss during spinal cord injury therapy. Sci Adv 2020; 6(14):eaaz1039.

[207]

Du X, Zhang S, Khabbaz A, Cohen KL, Zhang Y, Chakraborty S, et al. Regeneration of propriospinal axons in rat transected spinal cord injury through a growth-promoting pathway constructed by schwann cells overexpressing GDNF. Cells 2024; 13(13):1160.

[208]

David BT, Curtin JJ, Brown JL, Scorpio K, Kandaswamy V, Coutts DJC, et al. Temporary induction of hypoxic adaptations by preconditioning fails to enhance Schwann cell transplant survival after spinal cord injury. Glia 2023; 71(3):648-66.

[209]

Zheng X, Wang W. Astrocyte transplantation for repairing the injured spinal cord. J Biomed Res 2022; 36(5):312-20.

[210]

Chang J, Qian Z, Wang B, Cao J, Zhang S, Jiang F, et al. Transplantation of A2 type astrocytes promotes neural repair and remyelination after spinal cord injury. Cell Commun Signal 2023; 21(1):37.

[211]

Han GH, Kim SJ, Ko WK, Lee D, Han IB, Sheen SH, et al. Transplantation of tauroursodeoxycholic acid-inducing M2-phenotype macrophages promotes an anti-neuroinflammatory effect and functional recovery after spinal cord injury in rats. Cell Prolif 2021; 54(6):e13050.

[212]

Kobashi S, Terashima T, Katagi M, Nakae Y, Okano J, Suzuki Y, et al. Transplantation of M2-deviated microglia promotes recovery of motor function after spinal cord injury in mice. Mol Ther 2020; 28(1):254-65.

[213]

Gao W, Kim MW, Dykstra T, Du S, Boskovic P, Lichti CF, et al. Engineered T cell therapy for central nervous system injury. Nature 2024; 634(8034):693-701.

[214]

Correa S, Grosskopf AK, Lopez Hernandez H, Chan D, Yu AC, Stapleton LM, et al. Translational applications of hydrogels. Chem Rev 2021; 121(18):11385-457.

[215]

Xu L, Zhou S, Dai X, Gu X, Ouyang Z. Tissue engineering and spinal cord injury repair. Engineering 2025;46:60-72.

[216]

Zhou L, Guo P, D’Este M, Tong W, Xu J, Yao H, et al. Functionalized hydrogels for articular cartilage tissue engineering. Engineering 2022;13:71-90.

[217]

Luo Q, Sun J, Li Z, Liu B, Ding J. Thermo-sensitive poly(amino acid) hydrogel mediates cytoprotection through an antioxidant mechanism. Chin Chem Lett 2025; 36(7):110433.

[218]

Ju Y, Hu Y, Yang P, Xie X, Fang B. Extracellular vesicle-loaded hydrogels for tissue repair and regeneration. Mater Today Bio 2023;18:100522.

[219]

Mneimneh AT, Mehanna MM. Collagen-based scaffolds: an auspicious tool to support repair, recovery, and regeneration post spinal cord injury. Int J Pharm 2021;601:120559.

[220]

Wei Y, Zhou X, Li Z, Liu Q, Ding H, Zhou Y, et al. Genetically programmed single-component protein hydrogel for spinal cord injury repair. Adv Sci 2025; 12(10):e2405054.

[221]

Marchand R, Woerly S. Transected spinal cords grafted with in situ self-assembled collagen matrices. Neuroscience 1990; 36(1):45-60.

[222]

Tan Z, Xiao L, Ma J, Shi K, Liu J, Feng F, et al. Integrating hydrogels manipulate ECM deposition after spinal cord injury for specific neural reconnections via neuronal relays. Sci Adv 2024; 10(27):eado9120.

[223]

Liu G, Li S, Deng B, Huo L, Bai H, Jiang S, et al. Phase-separated anisotropic PVA hydrogel loaded with tetramethylpyrazine for spinal cord injury repair. Chem Eng J 2025;506:159944.

[224]

Duarte D, Correia C, Reis RL, Pashkuleva I, Peixoto D, Alves NM. Bioadhesive hyaluronic acid-based hydrogels for spinal cord injury. Biomacromolecules 2024; 25(3):1592-601.

[225]

Wu P, Xu C, Zou X, Yang K, Xu Y, Li X, et al. Capacitive-coupling-responsive hydrogel scaffolds offering wireless in situ electrical stimulation promotes nerve regeneration. Adv Mater 2024; 36(14):e2310483.

[226]

Zhong H, Zhou M, Guo J, Chen D, Xing C, Liu S, et al. Ultrasound-driven wireless piezoelectric hydrogel synergizes with cotransplantation of NSCs-hUCMSCs for structural and functional recovery in spinal cord injury. Mater Today Bio 2025;32:101805.

[227]

Hu Y, Wei H, Zhang H, Cheng H, Xu D, Wang H, et al. Magnetic nanochain-induced anisotropic nerve assembly for spinal cord injury repair. Chem Eng J 2024;501:157681.

[228]

Joung D, Lavoie NS, Guo SZ, Park SH, Parr AM, McAlpine MC. 3D printed neural regeneration devices. Adv Funct Mater 2020; 30(1):1906237.

[229]

Qiu C, Sun Y, Li J, Zhou J, Xu Y, Qiu C, et al. A 3D-printed dual driving forces scaffold with self-promoted cell absorption for spinal cord injury repair. Adv Sci 2023; 10(33):e2301639.

[230]

Liu X, Song S, Chen Z, Gao C, Li Y, Luo Y, et al. Release of O -GlcNAc transferase inhibitor promotes neuronal differentiation of neural stem cells in 3D bioprinted supramolecular hydrogel scaffold for spinal cord injury repair. Acta Biomater 2022;151:148-62.

[231]

Jiu J, Liu H, Li D, Li X, Zhang J, Yan L, et al. 3D mechanical response stem cell complex repairs spinal cord injury by promoting neurogenesis and regulating tissue homeostasis. Adv Healthc Mater 2025; 14(7):e2404925.

[232]

Tran KA, DeOre BJ, Ikejiani D, Means K, Paone LS, De Marchi L, et al. Matching mechanical heterogeneity of the native spinal cord augments axon infiltration in 3D-printed scaffolds. Biomaterials 2023;295:122061.

[233]

Bai B, Zhang R, Zhang C, Liu Y, Liu S, Zou C, et al. Spinal cord-like scaffold with rapid tissue integration enhanced spinal cord nerve repair. Adv Mater 2025:e05402.

[234]

Kwokdinata C, Chew SY. Additive manufacturing in spatial patterning for spinal cord injury treatment. Adv Drug Deliv Rev 2025;218:115523.

[235]

Joung D, Truong V, Neitzke CC, Guo SZ, Walsh PJ, Monat JR, et al. 3D printed stem-cell derived neural progenitors generate spinal cord scaffolds. Adv Funct Mater 2018; 28(39):1801850.

[236]

Wang X et al. Research progress of stimuli-responsive ZnO-based nanomaterials in biomedical applications. Biomater Sci 2022; 11(1):11.

[237]

Mehrotra S, Dey S, Sachdeva K, Mohanty S, Mandal BB. Recent advances in tailoring stimuli-responsive hybrid scaffolds for cardiac tissue engineering and allied applications. J Mater Chem B 2023; 11(43):10297-331.

[238]

Peng T, Chen Y, Hu W, Huang Y, Zhang M, Lu C, et al. Microneedles for enhanced topical treatment of skin disorders: applications, challenges, and prospects. Engineering 2023;30:170-89.

[239]

Zhou J, Fang C, Rong C, Luo T, Liu J, Zhang K. Reactive oxygen species-sensitive materials: a promising strategy for regulating inflammation and favoring tissue regeneration. Smart Mater Med 2023;4:427-46.

[240]

Eldahan KC, Rabchevsky AG. Autonomic dysreflexia after spinal cord injury: systemic pathophysiology and methods of management. Auton Neurosci 2018;209:59-70.

[241]

Cao J, Zhang X, Guo J, Wu J, Lin L, Lin X, et al. An engineering-reinforced extracellular vesicle-integrated hydrogel with an ROS-responsive release pattern mitigates spinal cord injury. Sci Adv 2025; 11(14):eads3398.

[242]

Chen H, Wang W, Yang Y, Zhang B, Li Z, Chen L, et al. A sequential stimuli-responsive hydrogel promotes structural and functional recovery of severe spinal cord injury. Biomaterials 2025;316:122995.

[243]

You Y, Jiang J, Zheng G, Chen Z, Zhu YX, Ma H, et al. In situ piezoelectric-catalytic anti-inflammation promotes the rehabilitation of acute spinal cord injury in synergy. Adv Mater 2024; 36(18):e2311429.

[244]

Li X, Li L, Wang D, Zhang J, Yi K, Su Y, et al. Fabrication of polymeric microspheres for biomedical applications. Mater Horiz 2024; 11(12):2820-55.

[245]

Feng Z, Zuo Y, Shen J, Zhao Q, Cao ZQ, Li X, et al. Bioengineering microspheres regulating mesenchymal stem cell fate accelerate spinal cord injury therapeutics. Nano Today 2025;61:102574.

[246]

Wang L, Gan J, Xu Z, Huang T, Zhou Y, Jiang X, et al. Laminin-modified porous GelMA microspheres sustain a pro-neurogenic niche for neural stem cells transplantation in spinal cord injury. Adv Funct Mater In press.

[247]

Ai Y, Hu C, Wang Y, Liu Y, Liu R, Xu H, et al. Core-shell hydrogel microspheres with sequential delivery of cerium oxide nanoparticles and spinal white matter extracellular matrix for improved functional recovery in spinal cord injury. Chem Eng J 2025;508:160861.

[248]

Liu X, Ma B, Hu S, Li D, Pan C, Xu Z, et al. Phase-adapted metal ion supply for spinal cord repair with a Mg-Zn incorporated chimeric microsphere. Biomaterials 2025;320:123253.

[249]

Shi B, Lu S, Yang H, Mahmood S, Sun C, Malek NANN, et al. One-dimensional nanomaterials for nerve tissue engineering to repair spinal cord injury. BMEmat 2025; 3(1):e12111.

[250]

Gao J, Khang M, Liao Z, Detloff M, Lee JS. Therapeutic targets and nanomaterial-based therapies for mitigation of secondary injury after spinal cord injury. Nanomedicine 2021; 16(22):2013-28.

[251]

Gao G, Li J, Ma Y, Xie M, Luo J, Wang K, et al. Dual-responsive multi-functional silica nanoparticles with repaired mitochondrial functions for efficient alleviation of spinal cord injury. Exploration 2025; 5(3):270012.

[252]

Sun H, Yang Y, Jin Y, Chen H, Li A, Chen X, et al. Novel nanocomposites improve functional recovery of spinal cord injury by regulating NF- j B mediated microglia polarization. Chem Eng J 2024;487:150633.

[253]

Kondiles BR, Wei H, Chaboub LS, Horner PJ, Wu JQ, Perlmutter SI. Transcriptome of rat subcortical white matter and spinal cord after spinal injury and cortical stimulation. Sci Data 2021; 8(1):175.

[254]

Amr SM, Gouda A, Koptan WT, Galal AA, Abdel-Fattah DS, Rashed LA, et al. Bridging defects in chronic spinal cord injury using peripheral nerve grafts combined with a chitosan-laminin scaffold and enhancing regeneration through them by co-transplantation with bone-marrow-derived mesenchymal stem cells: case series of 14 patients. J Spinal Cord Med 2014; 37(1):54-71.

[255]

Zhao Y, Tang F, Xiao Z, Han G, Wang N, Yin N, et al. Clinical study of neuroregen scaffold combined with human mesenchymal stem cells for the repair of chronic complete spinal cord injury. Cell Transplant 2017; 26(5):891-900.

[256]

Xiao Z, Tang F, Tang J, Yang H, Zhao Y, Chen B, et al. One-year clinical study of NeuroRegen scaffold implantation following scar resection in complete chronic spinal cord injury patients. Sci China Life Sci 2016; 59(7):647-55.

[257]

Tang F, Tang J, Zhao Y, Zhang J, Xiao Z, Chen B, et al. Long-term clinical observation of patients with acute and chronic complete spinal cord injury after transplantation of NeuroRegen scaffold. Sci China Life Sci 2022; 65(5):909-26.

[258]

Mie˛kisiak G, Ła˛tka D, Jarmuzek P, Załuski R, Urbański W, Janusz W. Steroids in acute spinal cord injury: all but gone within 5 years. World Neurosurg 2019;122:e467-71.

[259]

Wang X, Shen Z, Zhang H, Zhang HJ, Li F, Yu L, et al. Bexarotene improves motor function after spinal cord injury in mice. Neural Regen Res 2023; 18(12):2733-42.

[260]

Wu C, Chen Y, Chen X, Zhang Y, Zhao X, Deng Y, et al. 20-Deoxyingenol activates mitophagy through TFEB and promotes functional recovery after spinal cord injury. Mol Neurobiol 2025; 62(1):445-60.

[261]

Mishra MK, Kukal S, Paul PR, Bora S, Singh A, Kukreti S, et al. Insights into structural modifications of valproic acid and their pharmacological profile. Molecules 2021; 27(1):104.

[262]

Simmons EC, Scholpa NE, Schnellmann RG. FDA-approved 5-HT(1F) receptor agonist lasmiditan induces mitochondrial biogenesis and enhances locomotor and blood-spinal cord barrier recovery after spinal cord injury. Exp Neurol 2021;341:113720.

[263]

Wang X, Zhou T, Maynard G, Terse PS, Cafferty WB, Kocsis JD, et al. Nogo receptor decoy promotes recovery and corticospinal growth in non-human primate spinal cord injury. Brain 2020; 143(6):1697-713.

[264]

Maynard G, Kannan R, Liu J, Wang W, Lam TKT, Wang X, et al. Soluble Nogo-receptor-Fc decoy (AXER-204) in patients with chronic cervical spinal cord injury in the USA: a first-in-human and randomised clinical trial. Lancet Neurol 2023; 22(8):672-84.

[265]

Liu X, Pang Y, Fan B, Zhang J, Liu S, Deng X, et al. GPX4 activator enhances neuroprotection and functional recovery in spinal cord injury. J Orthop Translat 2025;52:344-59.

[266]

Chen B, Li Y, Yu B, Zhang Z, Brommer B, Williams PR, et al. Reactivation of dormant relay pathways in injured spinal cord by KCC2 manipulations. Cell 2018; 174(3):521-535.e13.

[267]

Davleeva MA, Garifulin RR, Bashirov FV, Izmailov AA, Nurullin LF, Salafutdinov II, et al. Molecular and cellular changes in the post-traumatic spinal cord remodeling after autoinfusion of a genetically-enriched leucoconcentrate in a mini-pig model. Neural Regen Res 2023; 18(7):1505-11.

[268]

Leibinger M, Zeitler C, Gobrecht P, Andreadaki A, Gisselmann G, Fischer D. Transneuronal delivery of hyper-interleukin-6 enables functional recovery after severe spinal cord injury in mice. Nat Commun 2021; 12(1):391.

[269]

Anderson MA, O’Shea TM, Burda JE, Ao Y, Barlatey SL, Bernstein AM, et al. Required growth facilitators propel axon regeneration across complete spinal cord injury. Nature 2018; 561(7723):396-400.

[270]

Squair JW, Milano M, de Coucy A, Gautier M, Skinnider MA, James ND, et al. Recovery of walking after paralysis by regenerating characterized neurons to their natural target region. Science 2023; 381(6664):1338-45.

[271]

Qu W, Wu X, Wu W, Wang Y, Sun Y, Deng L, et al. Chondroitinase ABC combined with Schwann cell transplantation enhances restoration of neural connection and functional recovery following acute and chronic spinal cord injury. Neural Regen Res 2025; 20(5):1467-82.

[272]

Kurian AG, Singh RK, Patel KD, Lee JH, Kim HW. Multifunctional GelMA platforms with nanomaterials for advanced tissue therapeutics. Bioact Mater 2022;8:267-95.

[273]

Kim KD, Lee KS, Coric D, Chang JJ, Harrop JS, Theodore N, et al. A study of probable benefit of a bioresorbable polymer scaffold for safety and neurological recovery in patients with complete thoracic spinal cord injury: 6-month results from the INSPIRE study. J Neurosurg Spine 2021; 34(5):808-17.

[274]

Anderson KD, Guest JD, Dietrich WD, Bartlett Bunge M, Curiel R, Dididze M, et al. Safety of autologous human Schwann cell transplantation in subacute thoracic spinal cord injury. J Neurotrauma 2017; 34(21):2950-63.

[275]

Zipser CM, Cragg JJ, Guest JD, Fehlings MG, Jutzeler CR, Anderson AJ, et al. Cell-based and stem-cell-based treatments for spinal cord injury: evidence from clinical trials. Lancet Neurol 2022; 21(7):659-70.

[276]

Bini TB, Gao S, Wang S, Ramakrishna S. Development of fibrous biodegradable polymer conduits for guided nerve regeneration. J Mater Sci - Mater Med 2005; 16(4):367-75.

[277]

Hu X, Xu W, Ren Y, Wang Z, He X, Huang R, et al. Spinal cord injury: molecular mechanisms and therapeutic interventions. Signal Transduct Target Ther 2023; 8(1):245.

[278]

Svendsen SP, Svendsen CN. Cell therapy for neurological disorders. Nat Med 2024; 30(10):2756-70.

[279]

Huang L, Sun X, Wang L, Pei G, Wang Y, Zhang Q, et al. Enhanced effect of combining bone marrow mesenchymal stem cells (BMMSCs) and pulsed electromagnetic fields (PEMF) to promote recovery after spinal cord injury in mice. MedComm 2022; 3(3):e160.

[280]

Jack AS, Hurd C, Forero J, Nataraj A, Fenrich K, Blesch A, et al. Cortical electrical stimulation in female rats with a cervical spinal cord injury to promote axonal outgrowth. J Neurosci Res 2018; 96(5):852-62.

[281]

Zareen N, Shinozaki M, Ryan D, Alexander H, Amer A, Truong DQ, et al. Motor cortex and spinal cord neuromodulation promote corticospinal tract axonal outgrowth and motor recovery after cervical contusion spinal cord injury. Exp Neurol 2017;297:179-89.

[282]

Lai BQ, Zeng X, Han WT, Che MT, Ding Y, Li G, et al. Stem cell-derived neuronal relay strategies and functional electrical stimulation for treatment of spinal cord injury. Biomaterials 2021;279:121211.

[283]

Chen KH, Dammann JF, Boback JL, Tenore FV, Otto KJ, Gaunt RA, et al. The effect of chronic intracortical microstimulation on the electrode-tissue interface. J Neural Eng 2014; 11(2):026004.

[284]

James ND, McMahon SB, Field-Fote EC, Bradbury EJ. Neuromodulation in the restoration of function after spinal cord injury. Lancet Neurol 2018; 17(10):905-17.

[285]

Guo Y, Duan W, Ma C, Jiang C, Xie Y, Hao H, et al. Biocompatibility and magnetic resonance imaging characteristics of carbon nanotube yarn neural electrodes in a rat model. Biomed Eng Online 2015; 14(1):118.

[286]

Bachmann LC, Matis A, Lindau NT, Felder P, Gullo M, Schwab ME. Deep brain stimulation of the midbrain locomotor region improves paretic hindlimb function after spinal cord injury in rats. Sci Transl Med 2013; 5(208):208ra146.

[287]

Evancho A, Tyler WJ, McGregor K. A review of combined neuromodulation and physical therapy interventions for enhanced neurorehabilitation. Front Hum Neurosci 2023;17:1151218.

[288]

Kumru H, Benito-Penalva J, Valls-Sole J, Murillo N, Tormos JM, Flores C, et al. Placebo-controlled study of rTMS combined with Lokomat(®) gait training for treatment in subjects with motor incomplete spinal cord injury. Exp Brain Res 2016; 234(12):3447-55.

[289]

Mertz L. FDA-cleared noninvasive spine stimulation system could transform spinal cord injury treatment. IEEE Pulse 2025; 16(3):10-5.

[290]

Adeel M, Lai CH, Lin BS, Chan WP, Liou JC, Wu CW, et al. Effects of paired stimulation with specific waveforms on cortical and spinal plasticity in subjects with a chronic spinal cord injury. J Formos Med Assoc 2022; 121(10):2044-56.

[291]

Kubinová Š. Biomaterials and magnetic stem cell delivery in the treatment of spinal cord injury. Neurochem Res 2020; 45(1):171-9.

[292]

Krucoff MO, Rahimpour S, Slutzky MW, Edgerton VR, Turner DA. Enhancing nervous system recovery through neurobiologics, neural interface training, and neurorehabilitation. Front Neurosci 2016;10:584.

[293]

Wang J, Wang T, Liu H, Wang K, Moses K, Feng Z, et al. Flexible electrodes for brain-computer interface system. Adv Mater 2023; 35(47):e2211012.

[294]

Li J, Ma Y, Huang D, Wang Z, Zhang Z, Ren Y, et al. High-performance flexible microneedle array as a low-impedance surface biopotential dry electrode for wearable electrophysiological recording and polysomnography. Nano-Micro Lett 2022; 14(1):132.

[295]

Ahmad Z, Salman S, Khan SA, Amin A, Rahman ZU, Al-Ghamdi YO, et al. Versatility of hydrogels: from synthetic strategies, classification, and properties to biomedical applications. Gels 2022; 8(3):167.

[296]

Fang M, Zhou J, Huang S, Zhang Y, He Y, Zeng Y, et al. Recombinant human erythropoietin plus methylprednisolone versus methylprednisolone in treatment of acute spinal cord injury: protocol for a systematic review and meta-analysis. BMJ Open 2022; 12(12):e056689.

[297]

Cheng H, Zhang H, Hu Y, Wang Y, Tian L, Qi Y, et al. Bioactive hydrogels loaded with BMSC-EXOs and GDNF for synergistically spinal cord injury repairing. Compos B Eng 2024;284:111618.

[298]

Cai J, Zhang H, Hu Y, Huang Z, Wang Y, Xia Y, et al. GelMA-MXene hydrogel nerve conduits with microgrooves for spinal cord injury repair. J Nanobiotechnology 2022; 20(1):460.

[299]

Wang J, Xie T, Long X, Gao R, Kang L, Wang Q, et al. The effect of tacrolimus-containing polyethylene glycol-modified maghemite nanospheres on reducing oxidative stress and accelerating the healing spinal cord injury of rats based on increasing M2 macrophages. Arab J Chem 2022; 15(1):103534.

[300]

Oudega M, Hao P, Shang J, Haggerty AE, Wang Z, Sun J, et al. Validation study of neurotrophin-3-releasing chitosan facilitation of neural tissue generation in the severely injured adult rat spinal cord. Exp Neurol 2019;312:51-62.

[301]

Suzuki H, Imajo Y, Funaba M, Ikeda H, Nishida N, Sakai T. Current concepts of biomaterial scaffolds and regenerative therapy for spinal cord injury. Int J Mol Sci 2023; 24(3):2528.

[302]

Winter CC, Katiyar KS, Hernandez NS, Song YJ, Struzyna LA, Harris JP, et al. Transplantable living scaffolds comprised of micro-tissue engineered aligned astrocyte networks to facilitate central nervous system regeneration. Acta Biomater 2016;38:44-58.

[303]

Li Q, Fu X, Kou Y, Han N. Engineering strategies and optimized delivery of exosomes for theranostic application in nerve tissue. Theranostics 2023; 13(12):4266-86.

[304]

Han M, Yang H, Lu X, Li Y, Liu Z, Li F, et al. Three-dimensional-cultured MSC-derived exosome-hydrogel hybrid microneedle array patch for spinal cord repair. Nano Lett 2022; 22(15):6391-401.

[305]

Xu D, Fu S, Zhang H, Lu W, Xie J, Li J, et al. Ultrasound-responsive aligned piezoelectric nanofibers derived hydrogel conduits for peripheral nerve regeneration. Adv Mater 2024; 36(28):2307896.

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