| Literature DB >> 33772754 |
P Cipriani1, R Giacomelli2, P Di Benedetto3, P Ruscitti1, O Berardicurti1, M Vomero2, L Navarini2, V Dolo4.
Abstract
Systemic sclerosis (SSc) is an autoimmune disease characterized by significant vascular alterations and multi-organ fibrosis. Microvascular alterations are the first event of SSc and injured endothelial cells (ECs) may transdifferentiate towards myofibroblasts, the cells responsible for fibrosis and collagen deposition. This process is identified as endothelial-to-mesenchymal transition (EndMT), and understanding of its development is pivotal to identify early pathogenetic events and new therapeutic targets for SSc. In this review, we have highlighted the molecular mechanisms of EndMT and summarize the evidence of the role played by EndMT during the development of progressive fibrosis in SSc, also exploring the possible therapeutic role of its inhibition.Entities:
Keywords: endothelial cells; endothelial-to-mesenchymal transition; systemic sclerosis
Mesh:
Year: 2021 PMID: 33772754 PMCID: PMC8209570 DOI: 10.1111/cei.13599
Source DB: PubMed Journal: Clin Exp Immunol ISSN: 0009-9104 Impact factor: 5.732