Hi Krishna I did similar exp many years ago. What we did was to isolate cells from 5 day old rats using trypsinization. Cells were then centrifuged and suspended in culture medium. The cells were incubated in a culture dish to allow mesenchymal cells to bind to dish. I cannot remember the incubation time as this was about 35 years ago. After the initial incubation, the cells that were not bound in the initial incubation were counted and seeded into plates. Medium was changed every 3 days. After 5-7 days a person see synchronous beating of the cardiomyocyte clusters. The method used is described in the following paper: T. Chajek, O. Stein, Y. Stein, Lipoprotein lipase of cultured mesenchymal rat heart cells, Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, Volume 528, Issue 3, 1978, Pages 466-474
Hi Krishna, I isolated neonatal rat cardiomyocytes every weeks with a kit of extraction. After 3 days, every cells, covering the culture surface, beats synchronously.
The cells which don't beat may be fibroblasts? Do you pre-plating the cell suspension to avoid cardiac fibroblasts?
What is the size of your culture dish? We noticed that the beats are best in plastic 6-well plate. It seems that in the smaller wells (96 well-plate or 24), the pacemaker cells may not be enough numerous to allow good beats. Therefore your hypothesis is plausible.
Do you seeding the cells at a concentration sufficient? Have you tested a growing range of seeding concentration?
Hi Krishna, I have used collagen dispersion method to isolate neonatal rat cardiomyocytes. The cells not beating in plates are not necessarily nonmyocytes. Beating of cells usually occurs when the cells are present in clusters or clumps., forming connections with each other. Isolated single cells usually do not beat. If you have any doubt, stain your cells with alpha sarcomeric actinin and count the number of actinin positive cells. A good isolation generally shows more than 90% actinin positive cells (myocytes).