In vitro Sex-specific Function-Structure Relationship in Neonatal Rat Cardiac Sheets

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The study developed an in vitro “heart-on-a-chip” platform using primary neonatal rat ventricular myocytes to examine sex chromosome–driven differences in cardiac monolayer structure and function without adding supplemented hormones. By allowing cardiomyocytes to self-assemble under controlled conditions, the authors found sex-specific divergence in both the contractile apparatus morphology and the functional properties of confluent monolayers. They report that this is the first characterization of sex-specific neonatal rat ventricular myocytes in in vitro culture. The paper’s main limitation is that it is an in vitro neonatal rat model, which may not capture full in vivo complexity. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract

ABSTRACT Even though in vivo rodent studies have been instrumental in investigating sex-specific differences in cardiac health, function, and pathology, they fall short in providing a fast and flexible platform for investigating sex differences of cardiac anisotropic monolayer in isolation. In vitro platforms offer an accessible and more controlled alternative to dissect and study the mechanisms by which male and female cardiac tissue sheets differ from one another. Here, we have shown on an in vitro heart-on-a-chip platform, primary neonatal rat ventricular myocytes can serve as a viable model showing sex chromosome-driven characteristics even in the absence of supplemented hormones. With controlled experimental conditions, the self-assembly of isolated cardiomyocytes resulted in morphological differences in the structure of the contractile apparatus. More importantly, the assembly of cardiac cells into confluent monolayers had a sex chromosome-driven divergence in both structure and the corresponding function. This work is the first characterization of the difference between sex-specific NRVMs in in vitro culture. Thus, this offers an avenue to investigate sex-based variations in cardiac function that are otherwise difficult to study.
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ABSTRACT Even though in vivo rodent studies have been instrumental in investigating sex-specific differences in cardiac health, function, and pathology, they fall short in providing a fast and flexible platform for investigating sex differences of cardiac anisotropic monolayer in isolation. In vitro platforms offer an accessible and more controlled alternative to dissect and study the mechanisms by which male and female cardiac tissue sheets differ from one another. Here, we have shown on an in vitro heart-on-a-chip platform, primary neonatal rat ventricular myocytes can serve as a viable model showing sex chromosome-driven characteristics even in the absence of supplemented hormones. With controlled experimental conditions, the self-assembly of isolated cardiomyocytes resulted in morphological differences in the structure of the contractile apparatus. More importantly, the assembly of cardiac cells into confluent monolayers had a sex chromosome-driven divergence in both structure and the corresponding function. This work is the first characterization of the difference between sex-specific NRVMs in in vitro culture. Thus, this offers an avenue to investigate sex-based variations in cardiac function that are otherwise difficult to study. Competing Interest Statement The authors have declared no competing interest.

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last seen: 2026-05-20T01:45:00.602351+00:00