Abstract
The female-predominate sex hormone 17β-estradiol exerts cardioprotective effects via multiple mechanisms. Available data demonstrate 17β-estradiol modulates microtubule dynamics in vitro, but its effects on pathogenic microtubule remodeling in pressure-overloaded cardiomyocytes are unexplored. Here, we show 17β-estradiol directly blunts microtubule polymerization in vitro, counteracts endothelin-mediated microtubule remodeling in iPSC-cardiomyocytes, and mitigates microtubule stabilization in pulmonary artery banded right ventricular cardiomyocytes. 17β-estradiol treatment blunts cardiomyocyte and nuclear hypertrophy, restores t-tubule architecture, and prevents mislocalization of connexin-43 in RV cardiomyocytes of pulmonary artery banded rats. These cellular phenotypes are paired with significant improvements in RV function. Thus, we propose 17β-estradiol exerts cardioprotective effects via direct modulation of microtubules in addition to its well ascribed signaling functions.
Competing Interest Statement
Dr. Prisco received personal fees from Merck. Dr. Prins obtained funding from Bayer. All other authors have no relevant disclosures.
Footnotes
Funding Sources Funding: JBM was funded by NIH T32 AR007612 and F31 HL170585, SZP was funded by NIH K08 HL168166 and an American Heart Association Career Development Award (23CDA1049093, https://doi.org/10.58275/AHA.23CDA1049093.pc.gr.167948), and KWP was funded by NIH R01s HL158795 and HL162927.
Conflict of Interest Disclosures Dr. Prisco received personal fees from Merck. Dr. Prins obtained funding from Bayer. All other authors have no relevant disclosures.