| Literature DB >> 33718407 |
Philip Chiu-Tsun Tang1, Alex Siu-Wing Chan2, Cai-Bin Zhang1, Cristina Alexandra García Córdoba1, Ying-Ying Zhang3, Ka-Fai To1, Kam-Tong Leung4, Hui-Yao Lan5,6, Patrick Ming-Kuen Tang1.
Abstract
Chronic kidney disease (CKD) is a major cause of morbidity and mortality worldwide, imposing a great burden on the healthcare system. Regrettably, effective CKD therapeutic strategies are yet available due to their elusive pathogenic mechanisms. CKD is featured by progressive inflammation and fibrosis associated with immune cell dysfunction, leading to the formation of an inflammatory microenvironment, which ultimately exacerbating renal fibrosis. Transforming growth factor β1 (TGF-β1) is an indispensable immunoregulator promoting CKD progression by controlling the activation, proliferation, and apoptosis of immunocytes via both canonical and non-canonical pathways. More importantly, recent studies have uncovered a new mechanism of TGF-β1 for de novo generation of myofibroblast via macrophage-myofibroblast transition (MMT). This review will update the versatile roles of TGF-β signaling in the dynamics of renal immunity, a better understanding may facilitate the discovery of novel therapeutic strategies against CKD.Entities:
Keywords: chronic kidney disease; immunity; kidney fibrosis; renal inflammation; transforming growth factor β
Year: 2021 PMID: 33718407 PMCID: PMC7948440 DOI: 10.3389/fmed.2021.628519
Source DB: PubMed Journal: Front Med (Lausanne) ISSN: 2296-858X