坏死性下垂
肝星状细胞
程序性细胞死亡
纤维化
自噬
肌成纤维细胞
电池类型
癌症研究
细胞外基质
医学
生物
细胞凋亡
细胞生物学
病理
细胞
生物化学
遗传学
作者
Min Hao,Xin Han,Zhouhui Yao,Han Zhang,Mengting Zhao,Mengyun Peng,Kuilong Wang,Hao Cai,Xianan Sang,Xin Wu,Lu Wang,Qiang Lv,Qiao Yang,Yini Bao,Haodan Kuang,Zhang Hong-yan,Gang Cao
摘要
Fibrosis is a common process of tissue repair response to multiple injuries in all chronic progressive diseases, which features with excessive deposition of extracellular matrix. Fibrosis can occur in all organs and tends to be nonreversible with the progress of the disease. Different cells types in different organs are involved in the occurrence and development of fibrosis, that is, hepatic stellate cells, pancreatic stellate cells, fibroblasts and myofibroblasts. Various types of programmed cell death, including apoptosis, autophagy, ferroptosis and necroptosis, are closely related to organ fibrosis. Among these programmed cell death types, necroptosis, an emerging regulated cell death type, is regarded as a huge potential target to ameliorate organ fibrosis. In this review, we summarize the role of necroptosis signalling in organ fibrosis and collate the small molecule compounds targeting necroptosis. In addition, we discuss the potential challenges, opportunities and open questions in using necroptosis signalling as a potential target for antifibrotic therapies. LINKED ARTICLES: This article is part of a themed issue on Translational Advances in Fibrosis as a Therapeutic Target. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v180.22/issuetoc.
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