Loading MiR-210 in Endothelial Progenitor Cells Derived Exosomes Boosts Their Beneficial Effects on Hypoxia/Reoxygeneation-Injured Human Endothelial Cells via Protecting Mitochondrial Function
Author(s) -
Xiaotang Ma,
Jinju Wang,
Jiao Li,
Chunlian Ma,
Shuzhen Chen,
Wei Lei,
Yi Yang,
Shiming Liu,
Ji Bihl,
Can Chen
Publication year - 2018
Publication title -
cellular physiology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.486
H-Index - 87
eISSN - 1421-9778
pISSN - 1015-8987
DOI - 10.1159/000488635
Subject(s) - mfn2 , endothelial progenitor cell , mitochondrial fission , microbiology and biotechnology , apoptosis , viability assay , transfection , progenitor cell , dnm1l , angiogenesis , mitochondrial ros , microvesicles , reactive oxygen species , flow cytometry , mitochondrial fusion , biology , mitochondrion , chemistry , microrna , stem cell , cell culture , cancer research , biochemistry , mitochondrial dna , genetics , gene
Stem cell-derived exosomes (EXs) offer protective effects on various cells via their carried microRNAs (miRs). Meanwhile, miR-210 has been shown to reduce mitochondrial reactive oxygen species (ROS) overproduction. In this study, we determined the potential effects of endothelial progenitor cell-derived EXs (EPC-EXs) on hypoxia/ reoxygenation (H/R) injured endothelial cells (ECs) and investigated whether these effects could be boosted by miR-210 loading.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom