The endothelial progenitor cells derived from Whartonâ??s jelly of human umbilical cord elicit protective effects on ischemic acute kidney injury in mice
4th International Conference and Exhibition on Cell & Gene Therapy
August 10-12, 2015 London, UK

Yuh-Lien Chen, Chan-Jung Liang and Fu-Bin Chang

Posters-Accepted Abstracts: J Stem Cell Res Ther

Abstract:

Acute kidney injury in humans has a high mortality and therapeutic options are limited, so the development of new potential
regenerative approaches as therapeutic strategies is highly desirable. The quality and the quantity of endothelial progenitor
cells (EPCs) that can be obtained from adult bone marrow and peripheral blood to treat renal diseases are limited. In this study,
we examined the therapeutic potential of implantation of EPCs isolated from Wharton’s jelly of human umbilical cord (WJC) in
the treatment of renal I/R injury in mice. Mesenchymal cells were isolated from WJC and cultured in endothelial growth medium.
Differentiation into EPCs was demonstrated by expression of the endothelial-specific markers and incorporation of acetylated lowdensity
lipoprotein. The present study demonstrated that EPCs improved renal function by the decrease in blood urea nitrogen and
creatinine levels in mice with renal I/R injury. Furthermore, EPC transplantation significantly attenuates renal apoptosis after I/R
injury as assessed by the TUNEL assay. This was closely associated with the inactivation of caspase 3 and the enhancement of antiapoptotic
marker Bcl-2 expression. In addition, EPC transplantation significantly reduced reactive oxygen species production and
the expression of the inflammatory cytokines (TNF-α, IL-1β) by immunohistochemistry and ELISA. Transplantation of EPCs from
WJC could provide a novel therapy for ischemic acute kidney injury by inhibiting apoptosis, ROS production and inflammation.