Cyclic mechanical strain promotes transforming-growth-factor-beta1-mediated cardiomyogenic marker expression in bone-marrow-derived mesenchymal stem cells in vitro

Biotechnol Appl Biochem. 2010 Apr 7;55(4):191-7. doi: 10.1042/BA20090307.

Abstract

Cardiomyocytes in the heart reside in mechanically dynamic environments, such as those subject to cyclic mechanical strain. TGF-beta1 (transforming growth factor-beta1) stimulates cardiomyogenic marker expression of BMMSCs (bone-marrow-derived mesenchymal stem cells). In the present study, we tested the hypothesis that cyclic mechanical strain promotes TGF-beta1-mediated cardiomyogenic marker expression in BMMSCs in vitro. The mRNA expression of cardiac-specific genes was more up-regulated in BMMSCs cultured with a TGF-beta1 supplement and subjected to cyclic strain for 1 week than in BMMSCs cultured statically with a TGF-beta1 supplement. Immunocytochemical analyses and flow cytometric analysis showed that the proportions of cardiac troponin-I-positive cells and cardiac MHC (myosin heavy chain)-positive cells and the proportions of cells expressing tropomyosin respectively were increased to a greater extent by TGF-beta1with cyclic strain than by TGF-beta1 alone. These results showed that cyclic strain promotes TGF-beta1mediated cardiomyogenic marker expression in BMMSCs in vitro.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Biomarkers / metabolism
  • Bone Marrow Cells / cytology
  • Bone Marrow Cells / metabolism
  • Cell Culture Techniques / methods*
  • Flow Cytometry
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / metabolism*
  • Myocytes, Cardiac / metabolism*
  • Myosin Heavy Chains / metabolism
  • Osteocalcin / genetics
  • Osteocalcin / metabolism
  • Osteonectin / genetics
  • Osteonectin / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Reverse Transcriptase Polymerase Chain Reaction
  • Shear Strength
  • Silicon / chemistry
  • Transforming Growth Factor beta1 / biosynthesis*
  • Troponin I / metabolism

Substances

  • Biomarkers
  • Osteonectin
  • Tgfb1 protein, rat
  • Transforming Growth Factor beta1
  • Troponin I
  • Osteocalcin
  • Myosin Heavy Chains
  • Silicon