| Literature DB >> 34986347 |
Alsya J Affandi1, Tiago Carvalheiro2, Andrea Ottria2, Judith J de Haan3, Maike A D Brans3, Maarten M Brandt4, Ralph G Tieland2, Ana P Lopes2, Beatriz Malvar Fernández2, Cornelis P J Bekker2, Maarten van der Linden2, Maili Zimmermann2, Barbara Giovannone5, Catharina G K Wichers2, Samuel Garcia2, Michael de Kok6, Giuseppina Stifano7, Yan Juan Xu8, M Anna Kowalska9, Maaike Waasdorp6, Caroline Cheng8, Susan Gibbs10, Saskia C A de Jager3, Joel A G van Roon2, Timothy R D J Radstake2, Wioleta Marut11.
Abstract
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.Entities:
Keywords: CXCL4; bleomycin; endothelial-to-mesenchymal transition; fibrosis; inflammation; myofibroblast; systemic sclerosis
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Year: 2022 PMID: 34986347 DOI: 10.1016/j.celrep.2021.110189
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423