The hepatocyte growth factor/c-met pathway is a key determinant of the fibrotic kidney local microenvironment
Year: 2021
Type: article
Abstract: The kidney local microenvironment (KLM) plays a critical role in the pathogenesis of kidney fibrosis. However, the composition and regulation of a fibrotic KLM remain unclear. Through a multidisciplinary approach, we investigated the roles of the hepatocyte growth factor/c-met signaling pathway in regulating KLM formation in various chronic kidney disease (CKD) models. We performed a retrospective analysis of single-cell RNA sequencing data and determined that tubular epithelial cells and macrophages are two major cell populations in a fibrotic kidney. We then created a mathematical model that predicted loss of c-met in tubular cells would cause greater responses to injury than loss of c-met in macrophages. By generating c-met conditional knockout mice, we validated that loss of c-met influences epithelial plasticity, myofibroblast activation, and extracellular matrix synthesis/degradation, which ultimately determined the characteristics of the fibrotic KLM. Our findings open the possibility of designing effective therapeutic strategies to retard CKD.
Source: iScience
Language: English
Subfield: Nephrology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $3,000
Awards: Early and Transient Activation of Fibroblast Promotes Tubule Repair after Acute Kidney Injury., G225257668, URoL: Epigenetics 1: Control by Noncoding RNA, The formation of kidney local microenvironment after acute kidney injury., Tenancin-C as a major component of the fibrogenic niche, G5834561958, Central role of fibroblasts in kidney repair and disease after AKI, G6890264914, Pittsburgh Center for Kidney Research, Cellular and Molecular Mechanisms of Renal Fibrosis, Cancer Center Support Grant
OpenAlex ID: W3199298556
