肌成纤维细胞
心脏纤维化
细胞生物学
生物
上皮-间质转换
间充质干细胞
肺纤维化
纤维化
癌症研究
免疫学
伤口愈合
细胞外基质
医学
病理
下调和上调
生物化学
基因
作者
Alsya J. Affandi,Tiago Carvalheiro,Andrea Ottria,Judith J. de Haan,Maike A. D. Brans,Maarten M. Brandt,Ralph G. Tieland,Ana P. Lopes,Beatriz Fernández,Cornelis P. J. Bekker,Maarten van der Linden,Maili Zimmermann,Barbara Giovannone,Catharina G. K. Wichers,Samuel García,Michael de Kok,Giuseppina Stifano,Yan Xu,M. Anna Kowalska,Maaike Waasdorp
出处
期刊:Cell Reports
[Cell Press]
日期:2022-01-01
卷期号:38 (1): 110189-110189
被引量:52
标识
DOI:10.1016/j.celrep.2021.110189
摘要
Fibrosis is a major cause of mortality worldwide, characterized by myofibroblast activation and excessive extracellular matrix deposition. Systemic sclerosis is a prototypic fibrotic disease in which CXCL4 is increased and strongly correlates with skin and lung fibrosis. Here we aim to elucidate the role of CXCL4 in fibrosis development. CXCL4 levels are increased in multiple inflammatory and fibrotic mouse models, and, using CXCL4-deficient mice, we demonstrate the essential role of CXCL4 in promoting fibrotic events in the skin, lungs, and heart. Overexpressing human CXCL4 in mice aggravates, whereas blocking CXCL4 reduces, bleomycin-induced fibrosis. Single-cell ligand-receptor analysis predicts CXCL4 to affect endothelial cells and fibroblasts. In vitro, we confirm that CXCL4 directly induces myofibroblast differentiation and collagen synthesis in different precursor cells, including endothelial cells, by stimulating endothelial-to-mesenchymal transition. Our findings identify a pivotal role of CXCL4 in fibrosis, further substantiating the potential role of neutralizing CXCL4 as a therapeutic strategy.
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