纤维细胞与弥漫性肺实质疾病的发病机制。

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
{"title":"纤维细胞与弥漫性肺实质疾病的发病机制。","authors":"Borna Mehrad,&nbsp;Robert M Strieter","doi":"10.1186/1755-1536-5-S1-S22","DOIUrl":null,"url":null,"abstract":"<p><p>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. </p>","PeriodicalId":12264,"journal":{"name":"Fibrogenesis & Tissue Repair","volume":"5 Suppl 1","pages":"S22"},"PeriodicalIF":0.0000,"publicationDate":"2012-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/1755-1536-5-S1-S22","citationCount":"20","resultStr":"{\"title\":\"Fibrocytes and the pathogenesis of diffuse parenchymal lung disease.\",\"authors\":\"Borna Mehrad,&nbsp;Robert M Strieter\",\"doi\":\"10.1186/1755-1536-5-S1-S22\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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. </p>\",\"PeriodicalId\":12264,\"journal\":{\"name\":\"Fibrogenesis & Tissue Repair\",\"volume\":\"5 Suppl 1\",\"pages\":\"S22\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2012-06-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1186/1755-1536-5-S1-S22\",\"citationCount\":\"20\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fibrogenesis & Tissue Repair\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1186/1755-1536-5-S1-S22\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2012/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fibrogenesis & Tissue Repair","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/1755-1536-5-S1-S22","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2012/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 20

摘要

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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fibrocytes and the pathogenesis of diffuse parenchymal lung disease.

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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信