Sca-1+ stem cell survival and engraftment in the infarcted heart: dual role for preconditioning-induced connexin-43

Circulation. 2009 May 19;119(19):2587-96. doi: 10.1161/CIRCULATIONAHA.108.827691. Epub 2009 May 4.

Abstract

Background: We report that elevated connexin-43 (Cx-43) in stem cells preconditioned with insulin-like growth factor-1 (IGF-1) is cytoprotective and reprograms the cells for cardiomyogenic differentiation.

Methods and results: Sca-1+ cells were preconditioned with 100 nmol/L IGF-1 for 30 minutes followed by 8 hours of oxygen glucose deprivation to assess the cytoprotective effects of preconditioning. LDH release assay, cytochrome c release, and mitochondrial membrane potential assay showed improved survival of preconditioned Sca-1+ cells under oxygen glucose deprivation compared with nonpreconditioned Sca-1+ cells via PI3K/Akt-dependent caspase-3 downregulation. We observed PI3K/Akt-dependent upregulation of cardiac-specific markers including MEF-2c (2.5-fold), GATA4 (3.1-fold), and Cx-43 (3.5-fold). Cx-43 inhibition with specific RNA interference reduced cell survival under oxygen glucose deprivation and after transplantation. In vivo studies were performed in a female rat model of acute myocardial infarction (n=78). Animals were grouped to receive intramyocardially 70 microL Dulbecco modified Eagles medium without cells (group 1) or containing male 1 x 10(6) nonpreconditioned Sca-1+ cells (group 2) or preconditioned Sca-1+ (group 3) cells labeled with PKH26. Survival of the preconditioned Sca-1+ cells was 5.5-fold higher in group 3 compared with group 2 at 7 days after transplantation. Confocal imaging after actinin and Cx-43 specific immunostaining showed extensive engraftment and myogenic differentiation of preconditioned Sca-1+ cells. Compared with group 2, group 3 showed increased blood vessel density (22.3+/-1.7 per microscopic field; P<0.0001) and attenuated infarction size (23.3+/-3.6%; P=0.002). Heart function indices including ejection fraction (56.2+/-3.5; P=0.029) and fractional shortening (24.3+/-2.1; P=0.03) were improved in group 3 compared with group 2.

Conclusions: Preconditioning with IGF-1 reprograms Sca-1+ for prosurvival signaling and cardiomyogenic differentiation with an important role for Cx-43 in this process.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antigens, Ly / analysis
  • Apoptosis / drug effects
  • Apoptosis / physiology
  • Cell Hypoxia
  • Cells, Cultured / drug effects
  • Cells, Cultured / metabolism
  • Cells, Cultured / transplantation
  • Connexin 43 / genetics
  • Connexin 43 / physiology*
  • Female
  • Glucose / pharmacology
  • Insulin-Like Growth Factor I / pharmacology
  • Ischemic Preconditioning, Myocardial*
  • Male
  • Membrane Proteins / analysis
  • Mesenchymal Stem Cell Transplantation*
  • Mesenchymal Stem Cells / drug effects*
  • Mesenchymal Stem Cells / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Multipotent Stem Cells / drug effects*
  • Multipotent Stem Cells / metabolism
  • Multipotent Stem Cells / transplantation
  • Myocardial Infarction / pathology
  • Myocardial Infarction / physiopathology
  • Myocardial Infarction / surgery*
  • Phosphatidylinositol 3-Kinases / physiology
  • Phosphoinositide-3 Kinase Inhibitors
  • Proto-Oncogene Proteins c-akt / antagonists & inhibitors
  • Proto-Oncogene Proteins c-akt / physiology
  • RNA Interference
  • RNA, Small Interfering / pharmacology
  • Rats
  • Rats, Inbred F344
  • Recombinant Proteins / pharmacology
  • Signal Transduction / drug effects

Substances

  • Antigens, Ly
  • Connexin 43
  • Ly6a protein, mouse
  • Membrane Proteins
  • Phosphoinositide-3 Kinase Inhibitors
  • RNA, Small Interfering
  • Recombinant Proteins
  • Insulin-Like Growth Factor I
  • Akt1 protein, mouse
  • Proto-Oncogene Proteins c-akt
  • Glucose