Tabriz University of Medical Sciences Journal of Cardiovascular and Thoracic Research 2008-5117 13 2 2021 05 22 Gender-specific characteristics of hypertrophic response in cardiomyocytes derived from human embryonic stem cells 146 155 10.34172/jcvtr.2021.32 EN Shiva Ahmadvand https://orcid.org/0000-0003-2824-1204 Ali Osia Anna Meyfour Sara Pahlavan https://orcid.org/0000-0002-8854-2626 Journal Article 10.34172/jcvtr.2021.32 2021 02 02 2021 04 30 Introduction: Gender-specific phenotypes of the heart were reported with respect to both physiology and pathology. While most differences were associated with the sex hormones, differential expression of genes received special attention, particularly X-Y chromosomes’ genes. Methods: Here, we compared cardiogenesis by gene expression analysis of lineage specific markers and X-Y chromosomes’ genes, during in vitro differentiation of XY and XX human embryonic stem cells (hESC), in a hormone-free setup. Results: Downregulation of pluripotency marker (NANOG) and upregulation of cardiac mesoderm and progenitor markers (GATA4, TBX5, NKX2.5, ISL1) was remained temporally similar in differentiating XY and XX hESCs. Isoproterenol treatment of XY and XX hESC-derived cardiomyocytes (hESCCM) induced hypertrophy in a sex-specific manner, with female cardiomyocytes showing response at higher isoproterenol concentration and a later time point of differentiation. Interestingly, KDM5C as an X-linked gene, was markedly upregulated in both hypertrophied male and female cardiomyocytes. Conclusion: Collectively, our results indicated a temporally identical cardiogenesis, but more susceptibility of XY hESC-CM to hypertrophic stimulus in a hormone-free condition.