Ontology highlight
ABSTRACT: Background
Pulmonary fibrosis (PF), the end point of interstitial lung diseases, is characterized by myofibroblast over differentiation and excessive extracellular matrix accumulation, leading to progressive organ dysfunction and usually a terminal outcome. Studies have shown that umbilical cord-derived mesenchymal stromal cells (uMSCs) could alleviate PF; however, the underlying mechanism remains to be elucidated.Methods
The therapeutic effects of uMSC-derived extracellular vesicles (uMSC-EVs) on PF were evaluated using bleomycin (BLM)-induced mouse models. Then, the role and mechanism of uMSC-EVs in inhibiting myofibroblast differentiation were investigated in vivo and in vitro.Results
Treatment with uMSC-EVs alleviated the PF and enhanced the proliferation of alv
SUBMITTER: Shi L
PROVIDER: S-EPMC8041243 | biostudies-literature | 2021 Apr
REPOSITORIES: biostudies-literature