Ontology highlight
ABSTRACT: Background
Idiopathic pulmonary fibrosis (IPF) is characterized by the recruitment of lung fibroblasts to sites within the lung interstitium, along with the differentiation of myofibroblasts induced by transforming growth factor (TGF)-β1, a mediator of fibrosis, which, in turn, leads to accelerated contractile lung fibrotic processes with excessive extracellular matrix (ECM) deposition. Extracellular vesicles (EVs) are small particles released by cells that contain physiologically active substances, including messenger RNAs, microRNAs (miRNAs), and proteins. Although EVs derived from mesenchymal stem cells (MSCs) are expected to be a promising drug for various intractable diseases, including IPF, the underlying mechanisms remain elusive. In this study, we aimed to elucidate the mec
SUBMITTER: Sumiyoshi I
PROVIDER: S-EPMC12357429 | biostudies-literature | 2025 Aug
REPOSITORIES: biostudies-literature