PGRMC2 is a pressure-volume regulator critical for myocardial responses to stress in mice
Farideh Amirrad,
Vivian La,
Sharareh Ohadi,
Miram Albotaif,
Sha Webster,
James K. Pru,
Kiumars Shamloo,
Ashraf M. Mohieldin and
Surya M. Nauli ()
Additional contact information
Farideh Amirrad: Chapman University
Vivian La: Chapman University
Sharareh Ohadi: Chapman University
Miram Albotaif: Chapman University
Sha Webster: Chapman University
James K. Pru: University of Wyoming
Kiumars Shamloo: Chapman University
Ashraf M. Mohieldin: Chapman University
Surya M. Nauli: Chapman University
Nature Communications, 2025, vol. 16, issue 1, 1-17
Abstract:
Abstract Progesterone receptors are classified into nuclear and membrane-bound receptor families. Previous unbiased proteomic studies indicate a potential association between cardiac diseases and the progesterone receptor membrane-bound component-2 (PGRMC2); however, the role of PGRMC2 in the heart remains unknown. In this study, we use a heart-specific knockout (KO) mouse model (MyH6•Pgrmc2flox/flox) in which the Pgrmc2 gene was selectively deleted in cardiomyocytes. Here we show that PGRMC2 serves as a mediator of steroid hormones for rapid calcium signaling in cardiomyocytes to maintain cardiac contraction, sufficient stroke volume, and adequate cardiac output by regulating the cardiac pressure-volume relationship. The KO hearts from male and female mice exhibit an impairment in pressure-volume relationship. Under hypoxic conditions, this pressure-volume dysregulation progresses to congestive left and right ventricular failure in the KO hearts. Overall, we propose that PGRMC2 is a cardiac pressure-volume regulator to maintain normal cardiac physiology, especially during hypoxic stress.
Date: 2025
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-57707-8
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DOI: 10.1038/s41467-025-57707-8
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