Irreversibility of Pulmonary Fibrosis

被引:48
作者
Yu, Qing Yang [1 ]
Tang, Xiao Xiao [1 ,2 ]
机构
[1] Guangzhou Med Univ, Guangzhou Inst Resp Hlth, Natl Clin Res Ctr Resp Dis, Affiliated Hosp 1,Natl Ctr Resp Med,State Key Lab, Guangzhou, Peoples R China
[2] Guangzhou Lab, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
pulmonary fibrosis; irreversibility; pathogenesis; lung; INTERSTITIAL LUNG-DISEASE; EXPRESSION; DIFFERENTIATION; AUTOPHAGY; MODELS; CELLS; PROLIFERATION; PNEUMONITIS; PROGENITORS; PERSISTENCE;
D O I
10.14336/AD.2021.0730
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
: Pulmonary fibrosis, a kind of terminal pathological changes in the lung, is caused by aberrant wound healing, deposition of extracellular matrix (ECM), and eventually replacement of lung parenchyma by ECM. Pulmonary fibrosis induced by acute lung injury and somediseases isreversible under treatment. While idiopathic pulmonary fibrosis is persistent and irreversible even after treatment. Currently, the pathogenesis of irreversible pulmonary fibrosis is not fully elucidated. The known factors associated with the development of irreversiblefibrosis include apoptosis resistance of (myo)fibroblasts, dysfunction of pulmonary vessel, cell mitochondria and autophagy, aberrant epithelia hyperplasia and lipid metabolism disorder. In this review, other than a brief introduction of reversible pulmonary fibrosis, we focus onthe underlying pathogenesis of irreversible pulmonary fibrosis from the above aspects as well aspreclinical disease models, and also suggestdirections for future studies
引用
收藏
页码:73 / 86
页数:14
相关论文
共 120 条
[1]   Club cells inhibit alveolar epithelial wound repair via TRAIL-dependent apoptosis [J].
Akram, Khondoker M. ;
Lomas, Nicola J. ;
Spiteri, Monica A. ;
Forsyth, Nicholas R. .
EUROPEAN RESPIRATORY JOURNAL, 2013, 41 (03) :683-694
[2]   NOX4/NADPH oxidase expression is increased in pulmonary fibroblasts from patients with idiopathic pulmonary fibrosis and mediates TGFβ1-induced fibroblast differentiation into myofibroblasts [J].
Amara, Nadia ;
Goven, Delphine ;
Prost, Fabienne ;
Muloway, Rachel ;
Crestani, Bruno ;
Boczkowski, Jorge .
THORAX, 2010, 65 (08) :733-738
[3]   Insufficient autophagy in idiopathic pulmonary fibrosis [J].
Araya, Jun ;
Kojima, Jun ;
Takasaka, Naoki ;
Ito, Saburo ;
Fujii, Satoko ;
Hara, Hiromichi ;
Yanagisawa, Haruhiko ;
Kobayashi, Kenji ;
Tsurushige, Chikako ;
Kawaishi, Makoto ;
Kamiya, Noriki ;
Hirano, Jun ;
Odaka, Makoto ;
Morikawa, Toshiaki ;
Nishimura, Stephen L. ;
Kawabata, Yoshinori ;
Hano, Hiroshi ;
Nakayama, Katsutoshi ;
Kuwano, Kazuyoshi .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2013, 304 (01) :L56-L69
[4]   You Say You Want a Resolution (of Fibrosis) [J].
Atabai, Kamran ;
Yang, Christopher D. ;
Podolsky, Michael J. .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2020, 63 (04) :424-435
[5]   Stuck in a Moment: Does Abnormal Persistence of Epithelial Progenitors Drive Pulmonary Fibrosis? [J].
Auyeung, Vincent C. ;
Sheppard, Dean .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2021, 203 (06) :667-669
[6]   Protein Tyrosine Phosphatase-N13 Promotes Myofibroblast Resistance to Apoptosis in Idiopathic Pulmonary Fibrosis [J].
Bamberg, Alison ;
Redente, Elizabeth F. ;
Groshong, Steve D. ;
Tuder, Rubin M. ;
Cool, Carlyne D. ;
Keith, Rebecca C. ;
Edelman, Benjamin L. ;
Black, Bart P. ;
Cosgrove, Gregory P. ;
Wynes, Murry W. ;
Curran-Everett, Douglas ;
De langhe, Stijn ;
Ortiz, Luis A. ;
Thorburn, Andrew ;
Riches, David W. H. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2018, 198 (07) :914-927
[7]   Linking Parenchymal disease progression to changes in lung mechanical function by percolation [J].
Bates, Jason H. T. ;
Davis, Gerald S. ;
Majumdar, Arnab ;
Butnor, Kelly J. ;
Suki, Bela .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2007, 176 (06) :617-623
[8]   Exploring efficacy and safety of oral Pirfenidone for progressive, non-IPF lung fibrosis (RELIEF) - a randomized, double-blind, placebo-controlled, parallel group, multi-center, phase II trial [J].
Behr, Juergen ;
Neuser, Petra ;
Prasse, Antje ;
Kreuter, Michael ;
Rabe, Klaus ;
Schade-Brittinger, Carmen ;
Wagner, Jasmin ;
Guenther, Andreas .
BMC PULMONARY MEDICINE, 2017, 17
[9]   Number and proliferation of Clara cells in normal human airway epithelium [J].
Boers, JE ;
Ambergen, AW ;
Thunnissen, FBJM .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 159 (05) :1585-1591
[10]   PINK1 deficiency impairs mitochondrial homeostasis and promotes lung fibrosis [J].
Bueno, Marta ;
Lai, Yen-Chun ;
Romero, Yair ;
Brands, Judith ;
Croix, Claudette M. St. ;
Kamga, Christelle ;
Corey, Catherine ;
Herazo-Maya, Jose D. ;
Sembrat, John ;
Lee, Janet S. ;
Duncan, Steve R. ;
Rojas, Mauricio ;
Shiva, Sruti ;
Chu, Charleen T. ;
Mora, Ana L. .
JOURNAL OF CLINICAL INVESTIGATION, 2015, 125 (02) :521-538