Fibrocytes and the pathogenesis of diffuse parenchymal lung disease.

Fibrogenesis & Tissue Repair Pub Date : 2012-06-06 eCollection Date: 2012-01-01 DOI:10.1186/1755-1536-5-S1-S22
Borna Mehrad, Robert M Strieter
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引用次数: 20

Abstract

Fibrosis is fundamental to the pathogenesis of many chronic lung diseases, including some lung infections, airway diseases such as bronchiectasis and asthma, and most of the diffuse parenchymal lung diseases. Idiopathic pulmonary fibrosis, the prototypical fibrotic lung disease, is amongst the most common diffuse parenchymal lung diseases and is characterized by progressive decline in lung function and premature death from respiratory failure. The clinical management of patients with this illness is hampered by our current inability to predict clinical deterioration and lack of an effective therapy. Fibrocytes are a population of bone marrow-derived circulating progenitor cells that home to injured tissues and differentiate into fibroblasts and myofibroblasts, thus contributing to scar formation. We summarize the evidence supporting the role of these cells in the pathogenesis of fibrotic lung diseases.

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纤维细胞与弥漫性肺实质疾病的发病机制。
纤维化是许多慢性肺部疾病发病的基础,包括一些肺部感染、支气管扩张和哮喘等气道疾病以及大多数弥漫性肺实质疾病。特发性肺纤维化是典型的肺纤维化疾病,是最常见的弥漫性肺实质疾病之一,其特征是肺功能进行性下降和呼吸衰竭导致的过早死亡。由于我们目前无法预测临床恶化和缺乏有效的治疗方法,对这种疾病患者的临床管理受到阻碍。纤维细胞是一种骨髓来源的循环祖细胞群,它们可返回损伤组织并分化为成纤维细胞和肌成纤维细胞,从而促进瘢痕形成。我们总结了支持这些细胞在纤维化肺疾病发病机制中的作用的证据。
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