With their rapid mode of action within only two hours in the kidney, the researchers deduced that the mechanism mediating the protective effects of MSC (mesenchymal stem cells) "must be primarily paracrine, as implied by their demonstrated expression of several growth factors such as HGF (hepatocyte growth factor), VEGF and IGF-1, all known to improve renal function in ARF, mediated by their antiapoptotic, mitogenic and other cytokine actions," the paper said.
"Specifically, these as yet incompletely defined paracrine actions of MSC result in the renal downregulation of proinflammatory cytokines IL-1-beta, TNF-alpha, and IFN-gamma, as well as iNOS (inducible nitric oxide synthase), and upregulation of anti-inflammatory and organ-protective interleukin-10, as well as bFGF (basic fibroblast growth factor), TGF-alpha (transforming growth factor alpha) and antiapoptotic Bc1-2," the paper added.
Beneficial paracrine actions are elicited early and late after onset of ARF
The study said it "provides the first clear evidence that therapy with MSC affords significant renoprotection in rats with ischemic/reperfusion (I/R) ARF. Animals infused with MSC either immediately or 24 hours after reperfusion had significantly better renal function, lower renal injury and cell-death scores, and higher cell division indices than vehicle-treated control animals," the paper stated. Indeed, administration after 24 hours of more severe ARF had an even greater beneficial effect.
Based on uti
Source:American Physiological Society