[1] |
T.M. Maher, E. Bendstrup, L. Dron, J. Langley, G. Smith, J.M. Khalid, et al. Global incidence and prevalence of idiopathic pulmonary fibrosis. Respir Res, 22 (1) (2021), p. 197
|
[2] |
J.P. Hutchinson, T.M. McKeever, A.W. Fogarty, V. Navaratnam, R.B. Hubbard. Increasing global mortality from idiopathic pulmonary fibrosis in the twenty-first century. Ann Am Thorac Soc, 11 (8) (2014), pp. 1176-1185
|
[3] |
T.E. King Jr, A. Pardo, M. Selman. Idiopathic pulmonary fibrosis. Lancet, 378 (9807) (2011), pp. 1949-1961
|
[4] |
V.Z. Beachley, M.T. Wolf, K. Sadtler, S.S. Manda, H. Jacobs, M.R. Blatchley, et al. Tissue matrix arrays for high-throughput screening and systems analysis of cell function. Nat Methods, 12 (12) (2015), pp. 1197-1204
|
[5] |
N.C. Henderson, F. Rieder, T.A. Wynn. Fibrosis: from mechanisms to medicines. Nature, 587 (7835) (2020), pp. 555-566
|
[6] |
C. Onursal, E. Dick, I. Angelidis, H.B. Schiller, C.A. Staab-Weijnitz. Collagen biosynthesis, processing, and maturation in lung ageing. Frontiers in Medicine, 20 (8) (2021), Article 593874
|
[7] |
M. Selman, A. Pardo. Revealing the pathogenic and aging-related mechanisms of the enigmatic idiopathic pulmonary fibrosis an integral model. Am J Respir Crit Care Med, 189 (10) (2014), pp. 1161-1172
|
[8] |
G. Raghu, S.Y. Chen, Q. Hou, W.S. Yeh, H.R. Collard. Incidence and prevalence of idiopathic pulmonary fibrosis in US adults 18-64 years old. Eur Respir J, 48 (1) (2016), pp. 179-186
|
[9] |
C. Lopez-Otin, M.A. Blasco, L. Partridge, M. Serrano, G. Kroemer. The hallmarks of aging. Cell, 153 (6) (2013), pp. 1194-1217
|
[10] |
S. Meiners, O. Eickelberg, M. Koenigshoff. Hallmarks of the ageing lung. Eur Respir J, 45 (3) (2015), pp. 807-827
|
[11] |
W.I. Choi, S. Dauti, H.J. Kim, S.H. Park, J.S. Park, C.W. Lee. Risk factors for interstitial lung disease: a 9-year nationwide population-based study. BMC Pulm Med, 18 (1) (2018), p. 96
|
[12] |
K. Shenderov, S.L. Collins, J.D. Powell, M.R. Horton. Immune dysregulation as a driver of idiopathic pulmonary fibrosis. J Clin Invest, 131 (2) (2021), Article e143226
|
[13] |
P. Heukels, C.C. Moor, J.H. von der Thusen, M.S. Wijsenbeek, M. Kool. Inflammation and immunity in IPF pathogenesis and treatment. Respir Med, 147 (2019), pp. 14779-14791
|
[14] |
G. Raghu, K.J. Anstrom, T.E. King Jr, J.A. Lasky, F.J. Martinez.Idiopathic pulm fibrosis C. Prednisone, azathioprine, and N-acetylcysteine for pulmonary fibrosis. Engl J Med, 366 (21) (2012), pp. 1968-1977
|
[15] |
F.J. Martinez, H.R. Collard, A. Pardo, G. Raghu, L. Richeldi, M. Selman, et al. Idiopathic pulmonary fibrosis. Nat Rev Dis Primers, 20 (3) (2017), p. 17074
|
[16] |
Y. Enomoto, T. Takemura, E. Hagiwara, T. Iwasawa, K. Okudela, N. Yanagawa, et al. Features of usual interstitial pneumonia in patients with primary Sjogren’s syndrome compared with idiopathic pulmonary fibrosis. Respir Investig, 52 (4) (2014), pp. 227-235
|
[17] |
M.J. Schafer, T.A. White, K. Iijima, A.J. Haak, G. Ligresti, E.J. Atkinson, et al. Cellular senescence mediates fibrotic pulmonary disease. Nat Commun, 23 (8) (2017), p. 14532
|
[18] |
J.M. van Deursen. The role of senescent cells in ageing. Nature, 509 (7501) (2014), pp. 439-446
|
[19] |
C. Yao, X. Guan, G. Carraro, T. Parimon, X. Liu, G. Huang, et al. Senescence of alveolar stem cells drives progressive pulmonary fibrosis. Am J Respir Crit Care Med, 203 (6) (2021), pp. 707-717
|
[20] |
M. Selman, C. Lopez-Otin, A. Pardo. Age-driven developmental drift in the pathogenesis of idiopathic pulmonary fibrosis. Eur Respir J, 48 (2) (2016), pp. 538-552
|
[21] |
R.P. Naikawadi, S. Disayabutr, B. Mallavia, M.L. Donne, G. Green, J.L. La, et al. Telomere dysfunction in alveolar epithelial cells causes lung remodeling and fibrosis. JCI Insight, 1 (14) (2016), Article e86704
|
[22] |
Y. Xu, T. Mizuno, A. Sridharan, Y. Du, M. Guo, J. Tang, et al. Single-cell RNA sequencing identifies diverse roles of epithelial cells in idiopathic pulmonary fibrosis. JCI Insight, 1 (20) (2016), Article e90558
|
[23] |
J. Liang, Y. Zhang, T. Xie, N. Liu, H. Chen, Y. Geng, et al. Hyaluronan and TLR4 promote surfactant-protein-C-positive alveolar progenitor cell renewal and prevent severe pulmonary fibrosis in mice. Nat Med, 22 (11) (2016), pp. 1285-1293
|
[24] |
D. Munoz-Espin, M. Serrano. Cellular senescence: from physiology to pathology. Nat Rev Mol Cell Biol, 15 (7) (2014), pp. 482-496
|
[25] |
M. Selman, A. Pardo. The leading role of epithelial cells in the pathogenesis of idiopathic pulmonary fibrosis. Cell Signal, 66 (2020), Article 109482
|
[26] |
Y. Tian, H. Li, T. Qiu, J. Dai, Y. Zhang, J. Chen, et al. Loss of PTEN induces lung fibrosis via alveolar epithelial cell senescence depending on NF-κB activation. Aging Cell, 18 (1) (2019), p. e12858
|
[27] |
T. Parimon, C. Yao, B.R. Stripp, P.W. Noble, P. Chen. Alveolar epithelial type II cells as drivers of lung fibrosis in idiopathic pulmonary fibrosis. Int J Mol Sci, 21 (7) (2020), p. 2269
|
[28] |
Y. Enomoto, H. Katsura, T. Fujimura, A. Ogata, S. Baba, A. Yamaoka, et al. Autocrine TGF-β-positive feedback in profibrotic AT2-lineage cells plays a crucial role in non-inflammatory lung fibrogenesis. Nat Commun, 14 (1) (2023), p. 4956
|
[29] |
M. Lehmann, M. Korfei, K. Mutze, S. Klee, W. Skronska-Wasek, H.N. Alsafadi, et al. Senolytic drugs target alveolar epithelial cell function and attenuate experimental lung fibrosis ex vivo. Eur Respir J, 50 (2) (2017), Article 1602367
|
[30] |
C. Yao, X. Guan, G. Carraro, T. Parimon, X. Liu, G. Huang, et al. Senescence of alveolar type 2 cells drives progressive pulmonary fibrosis. Am J Respir Crit Care Med, 203 (6) (2021), pp. 707-717
|
[31] |
J. Pan, D. Li, Y. Xu, J. Zhang, Y. Wang, M. Chen, et al.. Inhibition of Bcl-2/xl with ABT-263 selectively kills senescent type II pneumocytes and reverses persistent pulmonary fibrosis induced by ionizing radiation in mice. Int J Radiat Oncol Biol Phys, 99 (2) (2017), pp. 353-361
|
[32] |
B. Piersma, R.A. Bank, M. Boersema. Signaling in fibrosis: TGF-β WNT, and YAP/TAZ converge. Frontiers in medicine, 3 (2) (2015), p. 59
|
[33] |
X.M. Meng, D.J. Nikolic-Paterson, H.Y. Lan. TGF-β: the master regulator of fibrosis. Nat Rev Nephrol, 12 (6) (2016), pp. 325-338
|
[34] |
R.L. Gieseck III, M.S. Wilson, T.A. Wynn. Type 2 immunity in tissue repair and fibrosis. Nat Rev Immunol, 18 (1) (2018), pp. 62-76
|
[35] |
N. Schaum, B. Lehallier, O. Hahn, R. Pálovics, S. Hosseinzadeh, S.E. Lee, et al. Ageing hallmarks exhibit organ-specific temporal signatures. Nature, 583 (7817) (2020), pp. 596-602
|
[36] |
J. Sun, X. Ding, S. Liu, X. Duan, H. Liang, T. Sun. Adipose-derived mesenchymal stem cells attenuate acute lung injury and improve the gut microbiota in septic rats. Stem Cell Res Ther, 11 (1) (2020), p. 384
|
[37] |
C. Wang, J. Xie, L. Zhao, X. Fei, H. Zhang, Y. Tan, et al. Alveolar macrophage dysfunction and cytokine storm in the pathogenesis of two severe COVID-19 patients. EBioMedicine, 57 (2020), Article 102833
|
[38] |
R. Quan, C. Shi, B. Fang, Y. Sun, T. Qu, X. Wang, et al. Age-dependent inflammatory microenvironment mediates alveolar regeneration. Int J Mol Sci, 25 (6) (2024), p. 3476
|
[39] |
F. Verrecchia, M.L. Chu, A. Mauviel. Identification of novel TGF-β/smad gene targets in dermal fibroblasts using a combined cdna microarray/promoter transactivation approach. J Biol Chem, 276 (20) (2001), pp. 17058-17062
|
[40] |
Walton KL, Johnson KE, Harrison CA. Targeting TGF-β mediated smad signaling for the prevention of fibrosis. Front Pharmacol 2017; 8:461.
|
[41] |
D. Peng, M. Fu, M. Wang, Y. Wei, X. Wei. Targeting TGF-β signal transduction for fibrosis and cancer therapy. Mol Cancer, 21 (1) (2022), p. 104
|
[42] |
G. Raghu, S.Y. Chen, W.S. Yeh, B. Maroni, Q. Li, Y.C. Lee, et al. Idiopathic pulmonary fibrosis in US medicare beneficiaries aged 65 years and older: incidence, prevalence, and survival, 2001-2011. Lancet Respir Med, 2 (7) (2014), pp. 566-572
|
[43] |
T. Zhu, Z. Ying, X. Zhang, H. Wang, H. Liu. Piceatannol-mediated JAK2/STAT3 signaling pathway inhibition contributes to the alleviation of oxidative injury and collagen synthesis during pulmonary fibrosis. Int Immunopharmacol, 111 (2022), Article 109107
|
[44] |
L. Bai, A. Li, C. Gong, X. Ning, Z. Wang. Protective effect of rutin against bleomycin induced lung fibrosis: involvement of TGF-β1/α-SMA/Col I and III pathway. Biofactors, 46 (4) (2020), pp. 637-644
|
[45] |
J.J. Osterholzer, P.J. Christensen, V. Lama, J.C. Horowitz, N. Hattori, N. Subbotina, et al. PAI-1 promotes the accumulation of exudate macrophages and worsens pulmonary fibrosis following type II alveolar epithelial cell injury. J Pathol, 228 (2) (2012), pp. 170-180
|
[46] |
P. Flevaris, D. Vaughan. The role of plasminogen activator inhibitor type-1 in fibrosis. Semin Thromb Hemost, 43 (2) (2017), pp. 169-177
|
[47] |
K. Takeshita, K. Yamamoto, M. Ito, T. Kondo, T. Matsushita, M. Hirai, et al. Increased expression of plasminogen activator inhibitor-1 with fibrin deposition in a murine model of aging, “klotho” mouse. Semin Thromb Hemost, 28 (6) (2002), pp. 545-553
|
[48] |
K. Yamamoto, K. Takeshita, H. Saito. Plasminogen activator inhibitor-1 in aging. Semin Thromb Hemost, 40 (6) (2014), pp. 652-659
|
[49] |
A.K. Ghosh, D.E. Vaughan. PAI-1 in tissue fibrosis. J Cell Physiol, 227 (2) (2012), pp. 493-507
|
[50] |
L. Zappa, R. Savady, G.N. Humphries, P.H. Sugarbaker. Interstitial pneumonitis following intrapleural chemotherapy. World J Surg Oncol, 12 (7) (2009), p. 17
|
[51] |
A.S. Marudamuthu, S.K. Shetty, Y.P. Bhandary, S. Karandashova, M. Thompson, V. Sathish, et al. Plasminogen activator inhibitor-1 suppresses profibrotic responses in fibroblasts from fibrotic lungs. J Biol Chem, 290 (15) (2015), pp. 9428-9441
|
[52] |
T.H. Sisson, M. Mendez, K. Choi, N. Subbotina, A. Courey, A. Cunningham, et al. Targeted injury of type II alveolar epithelial cells induces pulmonary fibrosis. Am J Respir Crit Care Med, 181 (3) (2010), pp. 254-263
|
[53] |
A.K. Min, M.K. Kim, H.Y. Seo, H.S. Kim, B.K. Jang, J.S. Hwang, et al. Alpha-lipoic acid inhibits hepatic PAI-1 expression and fibrosis by inhibiting the TGF-β signaling pathway. Biochem Biophys Res Commun, 393 (3) (2010), pp. 536-541
|