Brain derived neurotrophic factor contributes to the cardiogenic potential of adult resident progenitor cells in failing murine heart

PLoS One. 2015 Mar 23;10(3):e0120360. doi: 10.1371/journal.pone.0120360. eCollection 2015.

Abstract

Aims: Resident cardiac progenitor cells show homing properties when injected into the injured but not to the healthy myocardium. The molecular background behind this difference in behavior needs to be studied to elucidate how adult progenitor cells can restore cardiac function of the damaged myocardium. Since the brain derived neurotrophic factor (BDNF) moderates cardioprotection in injured hearts, we focused on delineating its regulatory role in the damaged myocardium.

Methods and results: Comparative gene expression profiling of freshly isolated undifferentiated Sca-1 progenitor cells derived either from heart failure transgenic αMHC-CyclinT1/Gαq overexpressing mice or wildtype littermates revealed transcriptional variations. Bdnf expression was up regulated 5-fold during heart failure which was verified by qRT-PCR and confirmed at protein level. The migratory capacity of Sca-1 cells from transgenic hearts was improved by 15% in the presence of 25 ng/ml BDNF. Furthermore, BDNF-mediated effects on Sca-1 cells were studied via pulsed Stable Isotope Labeling of Amino acids in Cell Culture (pSILAC) proteomics approach. After BDNF treatment significant differences between newly synthesized proteins in Sca-1 cells from control and transgenic hearts were observed for CDK1, SRRT, HDGF, and MAP2K3 which are known to regulate cell cycle, survival and differentiation. Moreover BDNF repressed the proliferation of Sca-1 cells from transgenic hearts.

Conclusion: Comparative profiling of resident Sca-1 cells revealed elevated BDNF levels in the failing heart. Exogenous BDNF (i) stimulated migration, which might improve the homing ability of Sca-1 cells derived from the failing heart and (ii) repressed the cell cycle progression suggesting its potency to ameliorate heart failure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult Stem Cells / cytology
  • Adult Stem Cells / metabolism*
  • Adult Stem Cells / physiology
  • Animals
  • Antigens, Ly / genetics
  • Antigens, Ly / metabolism
  • Brain-Derived Neurotrophic Factor / genetics
  • Brain-Derived Neurotrophic Factor / metabolism*
  • Cell Differentiation*
  • Cell Movement
  • Cell Proliferation
  • Cells, Cultured
  • Heart Failure / metabolism*
  • Human Umbilical Vein Endothelial Cells / metabolism
  • Humans
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Mice
  • Myocytes, Cardiac / cytology
  • Myocytes, Cardiac / metabolism
  • Myocytes, Cardiac / physiology

Substances

  • Antigens, Ly
  • Brain-Derived Neurotrophic Factor
  • Ly6a protein, mouse
  • Membrane Proteins

Associated data

  • GEO/GSE58577

Grants and funding

This work was supported by grants from the Enhancement of research competitiveness in molecular imaging (EnVision), Framework 7 (FKZ: CSA-SA_FP/-REGPOT 2010-1, Grant Nr: 264143) to S.B.F.