He Weichun, Dai Chunsun
Center for Kidney Disease, Second Affiliated Hospital, Nanjing Medical University, 262 North Zhongshan Road, Nanjing, 210003 China.
Curr Pathobiol Rep. 2015;3(2):183-192. doi: 10.1007/s40139-015-0077-z.
Fibrosis is defined as an excessive accumulation of extracellular matrix components that lead to the destruction of organ architecture and impairment of organ function. Moreover, fibrosis is an intricate process attributable to a variety of interlaced fibrogenic signals and intrinsic mechanisms of activation of myofibroblasts. Being the dominant matrix-producing cells in organ fibrosis, myofibroblasts may be differentiated from various types of precursor cells. Identification of the signal pathways that play a key role in the pathogenesis of fibrotic diseases may suggest potential therapeutic targets. Here, we emphasize several intracellular signaling pathways that control the activation of myofibroblasts and matrix production.
纤维化的定义是细胞外基质成分过度积聚,导致器官结构破坏和器官功能受损。此外,纤维化是一个复杂的过程,归因于多种交织的致纤维化信号和成肌纤维细胞激活的内在机制。成肌纤维细胞作为器官纤维化中主要的基质产生细胞,可由多种类型的前体细胞分化而来。鉴定在纤维化疾病发病机制中起关键作用的信号通路可能提示潜在的治疗靶点。在此,我们着重介绍几种控制成肌纤维细胞激活和基质产生的细胞内信号通路。