Studies on Differentiation of Cardiac Myoblast Induced by Co-culture with Isolated Neonatal Rat Cardiac Myocytes.
- Author:
Jeong Hyun PARK
1
;
Han Sol KANG
Author Information
1. Department of Anatomy, College of Medicine, Kangwon National University, Korea. jhpark@kangwon.ac.kr
- Publication Type:Original Article
- Keywords:
Cardiomyocyte;
Myoblast;
MEF2c;
Nkx2.5;
Cell transplantation;
Intercellular junction
- MeSH:
Animals;
Anoxia;
Cardiomyoplasty;
Cell Line;
Cell Transplantation;
Coculture Techniques*;
Connexin 43;
Desmosomes;
Gap Junctions;
Genetic Therapy;
Intercellular Junctions;
Myoblasts;
Myoblasts, Cardiac*;
Myocardial Ischemia;
Myocytes, Cardiac*;
Plasmids;
Rats*;
Regeneration;
Transcription Factors;
Transfection;
Troponin T
- From:Korean Journal of Anatomy
2004;37(1):19-30
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Cellular cardiomyoplasty has recently emerged as a potential new treatment of ischemic heart disease. Combining cellular cardiomyoplasty with gene therapy using myogenic transcription factor might facilitate myocardial regeneration. In this study, we engineered H9c2, L6 using plasmid vector to overexpress the transcription factor MEF2c, Nkx2.5 involved in cardiomyogenesis. We investigated 1) formation of intercellular junction in mono-culture and co-culture with cardiomyocyte for functional and structural synchronous contraction after transplantation, 2) differentiation into cardiomyocyte, 3) resistance to hypoxic condition. Each cell overexpressing MEF2 and Nkx2.5 was generated by gene transfection and clonal selection. CO-culture was performed that each cell line added over cultured cardiomyocyte. H9c2-MEF2c and H9c2-Nkx2.5 became long, spindle shape like cardiomyocyte. Troponin T, cardiac specific marker, was found spot-like pattern in H9c2-Nkx2.5. However, co-culture with cardiomyocyte did not induce differentiation all kinds of cells into cardiomyocyte. Connexin43, which is gap junction marker was increased in H9c2-MEF2c, H9c2-Nkx2.5, L6-MEF2c and L6-Nkx2.5. Especially, co-culture with cardiomyocyte resulted in elevation of connexin43 levels more than monoculture. Ultrastructurally, formations of gap junction and desmosome were found apparently in L6-Nkx2.5. Long-standing, strong, regular and more frequent contraction were observed in cardiomyocyte co-cultured with H9c2-MEF2c, H9c2-Nkx2.5, L6-MEF2c, L6-Nkx2.5, respectively. Neverthless, any cell did not have active contraction itself, but passive movement except cardiomyocyte. H9c2-MEF2c, L6-MEF2c and L6-Nkx2.5 had resistance to hypoxia compared with other groups. These results suggested that co-culture and overexpressions of MEF2c and Nkx2.5 induced differentiation into cardiomyocyte and played an important role on intercellular junction formation and hypoxic resistance. This would be a promising source of cellular cardiomyoplasty. Therefore, much more research would be essential for clinical application of cellular cardiomyoplasty and this study would be a basic source for further study of MEF2c and Nkx2.5 in cellular cardiomyoplasty.
