Sexually dimorphic role of estrogen receptor α in preserving right ventricular endothelial integrity
Right ventricular (RV) function and adaptation to afterload increase determine survival in pulmonary hypertension (PH). RV adaptation in PH is sexually dimorphic and more preserved in females, mediated by protective estrogen receptor (ER) signaling in cardiomyocytes. However, the effects of ER on RV endothelial cells (RVECs), a critical mediator of RV homeostasis and adaptation, are unknown. We hypothesized that ER exerts sexually dimorphic pro-angiogenic effects on RVECs in vitro and promotes RV vascularization in vivo. Compared to cells isolated from wild-type animals, RVECs from male and female rats with an ER loss-of-function mutation (ERMut) showed reduced ability to form pseudo-vascular networks and migrate. RVECs from female ERMut rats demonstrated increased apoptosis. In a PH model induced by monocrotaline (MCT), female ERMut rats exhibited increased RV hypertrophy and reduced RV capillary density before (10 days) and at the time of established PH (28 days). Capillary rarefaction was associated with increased RVEC apoptosis, and, as identified by single-nucleus RNA-sequencing, by a net loss of the endocardial RVEC sub-population. Differentially expressed gene analysis and pathway analysis identified that capillary and endocardial RVECs from female MCT-PH ERMut rats demonstrated decreased expression of migration pathways and increased expression of apoptosis pathways. These findings reveal a sex-specific endothelial-intrinsic role of ER that is essential for angiogenesis in the RV under both homeostatic and pathological conditions. This effect appears to stem from the enhanced survival and migration capacity of capillary and endocardial RVEC. Collectively, our results identify ER as a potential target for developing sex-specific RV-directed therapies in PH. Translational perspectiveEffects of ER on vascular function in RV failure induced by PH are poorly understood. We unveiled a novel sexually dimorphic role of ER in regulating RV vascularization and RVEC function. Single nucleus RNA-Sequencing in female wild-type and ER loss-of-function rats with PH identified 5 unique RVEC sub-populations under transcriptional control of ER. Our findings provide insights into previously undescribed pro-angiogenic, pro-migratory and anti-apoptotic roles of ER in female RVs and RVECs. Promoting RVEC migration or inhibiting RVEC apoptosis to enhance RV angiogenesis may be viable pathways to maintain RV function in PH patients of either sex. These findings offer novel opportunities and potential therapeutic avenues for preventing or treating RV failure.