Impact of growth factors on miogenic mouse cells proliferation and surface markers expression
Radvile Malickaitė1'2, Laimutė Jurgauskienė1' 2, Jolanta Bukauskaitė3
Background. Acute myocardial infarction is accompanied by increased levels of proinflammatory cytokines, including TNF-a. We aimed to analyze alternations in myogenic mouse stem cells profifera - tion as well as the surface expression of adhesion molecules and receptors, involved in cell differentiation and transendothelial migration.
Material and methods. Skeletal muscle derived myogenic cell lines were isolated from 2-4 week old mouse leg musculus. Cell proliferation was assessed by flow cytometry using BrdU Flow Kit (BD Biosciences, San Diego). Influence of cytokines of pharmacological potential TNF-a, G-CSF, SCF and G-CSF/SCF combination on myogenic mouse stem cells proliferation as well as surface molecules expression has been investigated.
Results. High (100 ng/ml) concentrations of TNF-a inhibited cells proliferation; no stimulation of cell cycle has been noticed while using growth factors (G-CSF, SCF and G-CSF/SCF combina - tion). Endothelial progenitor cell markers CD31 and CD146 were not expressed. Neither TNF-a, no G-CSF, SCF nor G-CSF/SCF combination has influenced the expression of adhesion molecule CD44. Expression of CD81 (TAPA-1) and CD9 were inhibited using TNF-a, and induced only by G-CSF/SCF combination. SCF ligand CD117 expression was found to be twice as high after the incubation with growth factors combination in comparison with controls.
Conclusions. It was shown, that high concentrations of proinflammatory cytokine TNF-a suppress myogenic stem cell proliferation, as well as adhesion receptors CD81 (TAPA-1) and CD9 expression. No significant effect of SCF (100 ng/ml) or G-CSF (100 ng/ml) on cell pro lif er a tion was es tab lished. The G-CSF/SCF combination (100 ng/ml each) activates trans-membrane protein with tyrosine kinase capacity SCF ligand CD117 expression on myoblast cell line.
Keywords: stem cell, cytokines, adhesion molecules.