Ontology highlight
ABSTRACT: Background
Renal ischemia-reperfusion (I/R) injury is a major cause of acute kidney injury (AKI), which is associated with high morbidity and mortality. AKI is a serious and costly medical condition. Effective therapy for AKI is an unmet clinical need, and molecular mechanisms underlying the interactions between an injured kidney and distant organs remain unclear. Therefore, novel therapeutic strategies should be developed.Methods
We directed the differentiation of human induced pluripotent stem (iPS) cells into endothelial progenitor cells (iEPCs), which were then applied for treating mouse AKI. The mouse model of AKI was induced by I/R injury.Results
We discovered that intravenously infused iEPCs were recruited to the injured kidney, expressed the mature endotheli
SUBMITTER: Shen WC
PROVIDER: S-EPMC6288873 | biostudies-literature | 2018 Dec
REPOSITORIES: biostudies-literature