Cardiomyocyte, also called myocardiocyte or cardiac myocyte, is a myocyte that resides in the heart and develops from myoblasts with a central nucleus [1]. It is mainly responsible for the contraction of the heart to effectively execute the contraction-relaxation cycle by an intricate network of contractile proteins and ion transporters for this work [2]. Cardiomyocyte is smaller than skeletal myocytes and has abundant sarcoplasm.
As mentioned before, the primary function of the heart is to pump blood efficiently by virtue of an orchestrated contraction–relaxation cycle of the working myocytes. Regulation of contractility of the individual cardiomyocytes is achieved by a spatially defined program of ion channels and exchangers that accurately control Ca2+ entry into and out of the cell and the sarcoplasmic reticulum (Figure 1).

Figure 1. Model of Ca2+ regulation in cardiomyocytes
*This diagram is derived from the publication on The International Journal of Biochemistry & Cell Biology [3]
Cardiomyocyte markers are detected during development and diseases to determine the presence of cardiomyocytes. They may include enzymes, isoenzymes, isoforms and muscle proteins. CUSABIO list most cardiomyocyte markers on the following table, and click to see all the related molecules/targets and research reagents of them.
References
[1] Whetzel PL, et al. BioPortal: enhanced functionality via new web services from the National Center for Biomedical Ontology to access and use ontologies in software applications [J]. Nucleic Acids Res. 39 (2011) W541–W545 (Web Server issue).
[2] Benjamin Keepers, Jiandong Liu, and Li Qian. What's in a cardiomyocyte – And how do we make one through reprogramming [J]? Biochim Biophys Acta Mol Cell Res. 2020. 1867(3): 118464.
[3] Elizabeth A. Woodcock; Scot J. Matkovich. Cardiomyocytes structure, function and associated pathologies [J]. The International Journal of Biochemistry & Cell Biology. 2005, 37(9), 0–1751.
[4] Pradhan, L., Genis, C., Scone, P., et al. Crystal Structure of the Human NKX2.5 Homeodomain in Complex with DNA Target [J]. Biochemistry. 2012, 51(32), 6312–6319.
[5] Koss, M., Bolze, A., Brendolan, A., et al. Congenital Asplenia in Mice and Humans with Mutations in a Pbx/Nkx2-5/p15 Module [J]. Developmental Cell. 2012, 22(5), 913–926.
Cardiovascular Biology
Cardiovascular Markers
Common Cardiovascular Diseases
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