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本文引用的文献

1
Vascular-Parenchymal Cross-Talk Promotes Lung Fibrosis through BMPR2 Signaling.血管-实质相互作用通过 BMPR2 信号促进肺纤维化。
Am J Respir Crit Care Med. 2023 Jun 1;207(11):1498-1514. doi: 10.1164/rccm.202109-2174OC.
2
Arterial remodelling in smokers and in patients with small airway disease and COPD: implications for lung physiology and early origins of pulmonary hypertension.吸烟者以及患有小气道疾病和慢性阻塞性肺疾病患者的动脉重塑:对肺生理学及肺动脉高压早期起源的影响
ERJ Open Res. 2022 Dec 5;8(4). doi: 10.1183/23120541.00254-2022. eCollection 2022 Oct.
3
Single cell meta-analysis of EndMT and EMT state in COVID-19.单细胞荟萃分析 COVID-19 中的 EndMT 和 EMT 状态。
Front Immunol. 2022 Sep 29;13:976512. doi: 10.3389/fimmu.2022.976512. eCollection 2022.
4
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Nat Commun. 2022 Jul 25;13(1):4170. doi: 10.1038/s41467-022-31890-4.
5
Vascular remodelling in idiopathic pulmonary fibrosis patients and its detrimental effect on lung physiology: potential role of endothelial-to-mesenchymal transition.特发性肺纤维化患者的血管重塑及其对肺生理的有害影响:内皮-间充质转化的潜在作用
ERJ Open Res. 2022 Mar 21;8(1). doi: 10.1183/23120541.00571-2021. eCollection 2022 Jan.
6
Outcomes and Incidence of PF-ILD According to Different Definitions in a Real-World Setting.真实世界中根据不同定义的PF-ILD的结局和发病率
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7
Role of endothelial cells in pulmonary fibrosis via SREBP2 activation.内皮细胞通过 SREBP2 激活在肺纤维化中的作用。
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Age-related changes in the local milieu of inflamed tissues cause aberrant neutrophil trafficking and subsequent remote organ damage.炎症组织局部微环境随年龄增长而发生的改变可导致中性粒细胞迁移异常,并继发远处器官损伤。
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血管对肺修复和纤维化的作用。

Vascular Contribution to Lung Repair and Fibrosis.

机构信息

Department of Medicine, Stritch School of Medicine, Loyola University Chicago, Chicago, Illinois; and.

Department of Medicine, Boston University School of Medicine, Boston, Massachusetts.

出版信息

Am J Respir Cell Mol Biol. 2023 Aug;69(2):135-146. doi: 10.1165/rcmb.2022-0431TR.

DOI:10.1165/rcmb.2022-0431TR
PMID:37126595
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10399144/
Abstract

Lungs are constantly exposed to environmental perturbations and therefore have remarkable capacity to regenerate in response to injury. Sustained lung injuries, aging, and increased genomic instability, however, make lungs particularly susceptible to disrepair and fibrosis. Pulmonary fibrosis constitutes a major cause of morbidity and is often relentlessly progressive, leading to death from respiratory failure. The pulmonary vasculature, which is critical for gas exchanges and plays a key role during lung development, repair, and regeneration, becomes aberrantly remodeled in patients with progressive pulmonary fibrosis. Although capillary rarefaction and increased vascular permeability are recognized as distinctive features of fibrotic lungs, the role of vasculature dysfunction in the pathogenesis of pulmonary fibrosis has only recently emerged as an important contributor to the progression of this disease. This review summarizes current findings related to lung vascular repair and regeneration and provides recent insights into the vascular abnormalities associated with the development of persistent lung fibrosis.

摘要

肺脏不断受到环境变化的影响,因此具有很强的再生能力以应对损伤。然而,持续的肺部损伤、衰老和基因组不稳定性使肺部特别容易出现修复缺陷和纤维化。肺纤维化是发病率的主要原因,且往往呈进行性发展,导致呼吸衰竭而死亡。肺部血管对于气体交换至关重要,并在肺发育、修复和再生过程中发挥关键作用,在进行性肺纤维化患者中会发生异常重塑。尽管毛细血管稀疏和血管通透性增加被认为是纤维化肺部的显著特征,但血管功能障碍在肺纤维化发病机制中的作用最近才被认为是导致该疾病进展的一个重要因素。本综述总结了与肺血管修复和再生相关的最新发现,并提供了与持续性肺纤维化发展相关的血管异常的最新见解。