PGRMC2 is a pressure-volume regulator critical for myocardial responses to stress in mice

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•Pgrmc2<sup>flox/flox</sup>) 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.

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Publication Details

Journal
Nature Communications
Published
2025-03-11
DOI
https://doi.org/10.1038/s41467-025-57707-8
Citations
1
Primary Topic
Cardiac Ischemia and Reperfusion
Type
article
Field-Weighted Citation Impact
1.47

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article

PGRMC2 is a pressure-volume regulator critical for myocardial responses to stress in mice

James K. Pru, Sha Webster, Ashraf M. Mohieldin, Kiumars Shamloo et al.
1 citations
Nature Communications
Cardiac Ischemia and Reperfusion
1.47
article

PGRMC2 is a pressure-volume regulator critical for myocardial responses to stress in mice

James K. Pru, Sha Webster, Ashraf M. Mohieldin, Kiumars Shamloo, Farideh Amirrad, Vivian La, Sharareh Ohadi, Miram Albotaif
article en
1 citations

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•Pgrmc2<sup>flox/flox</sup>) 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.

Nature CommunicationsVol. 16(1)
University of Wyoming (US), Chapman University (US), Marshall B. Ketchum University (US), University of California, Irvine (US), California Northstate University (US)
National Heart, Lung, and Blood Institute
Good health and well-being
Openalex Percentile: Top 22%
Cardiac Ischemia and Reperfusion
1.47
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