Mechanisms of fibrosis: therapeutic translation for fibrotic disease

被引:2609
作者
Wynn, Thomas A. [1 ]
Ramalingam, Thirumalai R. [1 ]
机构
[1] NIAID, Immunopathogenesis Sect, Program Barrier Immun & Repair, Parasit Dis Lab,NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
TUMOR-NECROSIS-FACTOR; REGULATORY T-CELLS; IDIOPATHIC PULMONARY-FIBROSIS; HEPATIC STELLATE-CELLS; TISSUE GROWTH-FACTOR; ENDOPLASMIC-RETICULUM STRESS; MESSENGER-RNA EXPRESSION; ACTIVATED RECEPTOR-GAMMA; PLACEBO-CONTROLLED TRIAL; ACUTE LUNG INJURY;
D O I
10.1038/nm.2807
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fibrosis is a pathological feature of most chronic inflammatory diseases. Fibrosis, or scarring, is defined by the accumulation of excess extracellular matrix components. If highly progressive, the fibrotic process eventually leads to organ malfunction and death. Fibrosis affects nearly every tissue in the body. Here we discuss how key components of the innate and adaptive immune response contribute to the pathogenesis of fibrosis. We also describe how cell-intrinsic changes in important structural cells can perpetuate the fibrotic response by regulating the differentiation, recruitment, proliferation and activation of extracellular matrix-producing myofibroblasts. Finally, we highlight some of the key mechanisms and pathways of fibrosis that are being targeted as potential therapies for a variety of important human diseases.
引用
收藏
页码:1028 / 1040
页数:13
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