Adult skeletal muscle stem cells differentiate into endothelial lineage and ameliorate renal dysfunction after acute ischemia

Am J Physiol Renal Physiol. 2004 Oct;287(4):F621-7. doi: 10.1152/ajprenal.00126.2004. Epub 2004 Jun 15.


We previously demonstrated that endothelial cells are severely damaged during renal ischemia-reperfusion and that transplantation of adult human endothelial cells into athymic nude rats subjected to renal ischemia resulted in a dramatic protection of the kidney against injury and dysfunction. Morphological studies demonstrated the engraftment of transplanted cells into renal microvasculature. The goal of the present study was to determine the potential efficacy of in vitro expanded skeletal muscle-derived stem cells (MDSC) differentiated along the endothelial lineage in ameliorating acute renal injury. MDSC obtained from the Tie-2-green fluorescent protein (GFP) mice were used as donors of differentiated and nondifferentiated stem cells. FVB mice, used as recipients, were subjected to renal ischemia and transplanted with the above MDSC. The differentiation of MDSC along the endothelial lineage was monitored by the appearance of Tie-2 promotor-driven expression of GFP. These mouse endothelial cell antigen-, endothelial nitric oxide synthase (eNOS)-, Flk-1-, Flt-1-, and CD31-positive cells engrafted into renal microvasculature and significantly protected short-term renal function after ischemia. Transplantation of nondifferentiated MDSC characterized by the expression of Sca-1 (low levels of CD34, Flk-1, and cKit, and negative for GFP, eNOS, and CD31) did not improve short-term renal dysfunction. In conclusion, the data 1) provide a rich source of MDSC, 2) delineate protocols for their in vitro expansion and differentiation along the endothelial lineage, and 3) demonstrate their efficacy in preserving renal function immediately after ischemic insult.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acute Disease
  • Age Factors
  • Animals
  • Cell Differentiation
  • Cell Lineage
  • Endothelial Cells / cytology
  • Endothelial Cells / transplantation*
  • Green Fluorescent Proteins
  • Ischemia / pathology
  • Ischemia / physiopathology
  • Ischemia / therapy*
  • Kidney Diseases / pathology
  • Kidney Diseases / physiopathology
  • Kidney Diseases / therapy*
  • Luminescent Proteins / genetics
  • Mice
  • Mice, Transgenic
  • Muscle, Skeletal / cytology*
  • Receptor, TIE-2 / genetics
  • Stem Cell Transplantation*
  • Stem Cells / cytology


  • Luminescent Proteins
  • Green Fluorescent Proteins
  • Receptor, TIE-2