Ontology highlight
ABSTRACT: Background
Extracellular vesicles (EVs) are recognized as novel cell-free therapeutics. Non-alcoholic steatohepatitis (NASH) remains a critical health problem. Herein, we show that EVs from pan peroxisome proliferator-activated receptor agonist-primed induced mesenchymal stem cell (pan PPAR-iMSC-EVs) has unique cargo protein signatures, and demonstrate its therapeutic function in NASH.Results
A unique protein signatures were identified in pan PPAR-iMSC-EVs against those from non-stimulated iMSC-EVs. NASH mice receiving pan PPAR-iMSC-EVs showed reduced steatotic changes and ameliorated ER stress and mitochondiral oxidative stress induced by inflammation. Moreover, pan PPAR-iMSC-EVs promoted liver regeneration via inhibiting apoptosis and enhancing proliferation.Conclusions
We conclude that our strategy for enriching unique cargo proteins in EVs may facilitate the development of novel therapeutic option for NASH.
SUBMITTER: Kim J
PROVIDER: S-EPMC8600817 | biostudies-literature | 2021 Nov
REPOSITORIES: biostudies-literature
Kim Jimin J Lee Seul Ki SK Jeong Seon-Yeong SY Cho Hye Jin HJ Park Joonghoon J Kim Tae Min TM Kim Soo S
Journal of nanobiotechnology 20211117 1
<h4>Background</h4>Extracellular vesicles (EVs) are recognized as novel cell-free therapeutics. Non-alcoholic steatohepatitis (NASH) remains a critical health problem. Herein, we show that EVs from pan peroxisome proliferator-activated receptor agonist-primed induced mesenchymal stem cell (pan PPAR-iMSC-EVs) has unique cargo protein signatures, and demonstrate its therapeutic function in NASH.<h4>Results</h4>A unique protein signatures were identified in pan PPAR-iMSC-EVs against those from non- ...[more]