The cardiac myocyte is the most physically energetic cell in the body. Its contraction is myogenic, i.e. it is independent of nervous stimulation. All cardiac myocyte are capable of spontaneous rhythmic depolarization and repolarization of their membrane. Cardiac myocytes occupy as much as 75% of cardiac mass but constitute only about one third of the total cell number in the heart. They are highly specialized high-oxygen-content cells and house a large number of mitochondria [1]. Differentiated cardiac myocytes have little capacity to proliferate and show the hypertrophic growth in response to alpha1-adrenergic stimuli via the Ras/MEK pathway [2]. Cardiac myocyte hypertrophy and apoptosis have been implicated in the loss of contractile function during heart failure. Cardiac myocytes have a complex network of signals that regulates their essential role in the rhythmic pumping of the heart [3]. This network is an appealing model system in which to study the basic principles of cellular signaling mechanisms leading to cardiac myocyte death.
HCM from ScienCell Research Laboratories are isolated from human heart tissue. HCM are cryopreserved immediately after purification and delivered frozen. Each vial contains >5 x 105 cells in 1 ml volume. HCM are characterized by immunofluorescent method with antibody to myosin. HCM are negative for HIV-1, HBV, HCV, mycoplasma, bacteria, yeast and fungi. HCM are guaranteed to further culture at the conditions provided by ScienCell Research Laboratories.
Recommended Medium
It is recommended to use Cardiac Myocyte Medium (CMM, Cat. No. 6201) for the culturing of HCM in vitro.
Product Use
HCM are for research use only. It is not approved for human or animal use, or for application in in vitro diagnostic procedures.
Storage
Directly and immediately transfer cells from dry ice to liquid nitrogen upon receiving and keep the cells in liquid nitrogen until cell culture needed for experiments.
Shipping
Dry ice.
Reference
[1] Bodyak, N., Kang, P. M., Hiromura, M., Sulijoadikusumo, I., Horikoshi, N., Khrapko, K. and Usheva, A. (2004) Gene expression profiling of the aging mouse cardiac myocytes. Nucleic Acids Research 30(17):3788-3794.
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Fig 1. Relief contrast morphology of cultured HCM, 200X.
Fig 2. Phase contrast morphology of cultured HCM. Note that cell clump or hill-like structure (middle of the picture) has been formed from monolayer of culture. The cells in the clump were beating, 200X.
Fig 3. Immunofluorescent staining of HCM with anti-alpha sarcomeric actinin antibody (green) and DAPI (blue), 200X.
Fig 3. Immunofluorescent staining of HCM with anti-myosin (skeletal, slow) antibody (green) and DAPI (blue), 200X.