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肺纤维化的不可逆性

Irreversibility of Pulmonary Fibrosis.

作者信息

Yu Qing Yang, Tang Xiao Xiao

机构信息

1State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, National Center for Respiratory Medicine, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.

2Guangzhou Laboratory, Bio-island, Guangzhou, China.

出版信息

Aging Dis. 2022 Feb 1;13(1):73-86. doi: 10.14336/AD.2021.0730. eCollection 2022 Feb.


DOI:10.14336/AD.2021.0730
PMID:35111363
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8782547/
Abstract

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 some diseases is reversible 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 irreversible fibrosis 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 on the underlying pathogenesis of irreversible pulmonary fibrosis from the above aspects as well as preclinical disease models, and also suggest directions for future studies.

摘要

肺纤维化是肺部的一种终末期病理变化,由异常的伤口愈合、细胞外基质(ECM)沉积引起,最终肺实质被ECM替代。急性肺损伤和某些疾病引起的肺纤维化在治疗下是可逆的。而特发性肺纤维化即使经过治疗仍持续且不可逆。目前,不可逆性肺纤维化的发病机制尚未完全阐明。已知与不可逆性纤维化发展相关的因素包括(肌)成纤维细胞的抗凋亡、肺血管功能障碍、细胞线粒体和自噬、上皮细胞异常增生以及脂质代谢紊乱。在本综述中,除了简要介绍可逆性肺纤维化外,我们将从上述方面以及临床前疾病模型重点关注不可逆性肺纤维化的潜在发病机制,并提出未来研究方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf17/8782547/11a48ae656ca/ad-13-1-73-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf17/8782547/47d83322c514/ad-13-1-73-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf17/8782547/11a48ae656ca/ad-13-1-73-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf17/8782547/47d83322c514/ad-13-1-73-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf17/8782547/11a48ae656ca/ad-13-1-73-g2.jpg

相似文献

[1]
Irreversibility of Pulmonary Fibrosis.

Aging Dis. 2022-2-1

[2]
Epithelium-dependent profibrotic milieu in the pathogenesis of idiopathic pulmonary fibrosis: current status and future directions.

Clin Respir J. 2016-3

[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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[5]
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[6]
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[7]
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[8]
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[10]
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本文引用的文献

[1]
Role of interleukins in the pathogenesis of pulmonary fibrosis.

Cell Death Discov. 2021-3-15

[2]
Club Cell Loss as a Feature of Bronchiolization in ILD.

Front Immunol. 2021

[3]
Spontaneous Lung Fibrosis Resolution Reveals Novel Antifibrotic Regulators.

Am J Respir Cell Mol Biol. 2021-4

[4]
Persistent, Progressive Pulmonary Fibrosis and Epithelial Remodeling in Mice.

Am J Respir Cell Mol Biol. 2021-6

[5]
Loss of Fas signaling in fibroblasts impairs homeostatic fibrosis resolution and promotes persistent pulmonary fibrosis.

JCI Insight. 2020-12-8

[6]
Reversible lung fibrosis in a 6-year-old girl after long term nitrofurantoin treatment.

BMC Pulm Med. 2020-11-26

[7]
Fibrosis: from mechanisms to medicines.

Nature. 2020-11

[8]
Stuck in a Moment: Does Abnormal Persistence of Epithelial Progenitors Drive Pulmonary Fibrosis?

Am J Respir Crit Care Med. 2021-3-15

[9]
New Perspectives on the Aberrant Alveolar Repair of Idiopathic Pulmonary Fibrosis.

Front Cell Dev Biol. 2020-9-30

[10]
Progressive fibrosing interstitial lung disease: a clinical cohort (the PROGRESS study).

Eur Respir J. 2021-2-11

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