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. 2025 Jun;4(6):710-726.
doi: 10.1038/s44161-025-00653-x. Epub 2025 May 19.

Mineralocorticoid receptor phase separation modulates cardiac preservation

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Mineralocorticoid receptor phase separation modulates cardiac preservation

Ienglam Lei et al. Nat Cardiovasc Res. 2025 Jun.

Abstract

Heart transplantation is the gold standard treatment for patients with end-stage heart failure. However, there is a shortage of donor hearts available. The short tolerable cold ischemic time for delivering donor hearts to matching recipients is closely responsible for this shortage. Here we uncover the phenomenon of mineralocorticoid receptor (MR) phase separation, which exacerbates injury to the murine and human donor heart during cold storage and can be modulated with pharmacological inhibition to improve preservation quality. Interestingly, donor cardiomyocytes strongly expressed MR, which undergoes preservation-related phase separation. The phenomenon of macromolecular phase separation is not limited to the heart or MR during preservation. Cold preservation of the lung, liver and kidney also displays phase separation of other transcriptional regulators including histone deacetylase 1 (HDAC1), bromodomain-containing 4 (BRD4) and MR. Our results reveal an understudied area of preservation biology that may be further exploited to improve the preservation of multiple solid organs.

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Conflict of interest statement

Competing interests: I.L., Z.W., F.D.P., B.P., Y.E.C. and P.C.T. have filed a US provisional patent (title: Histone-acetylation-modulating agents for the treatment and prevention of organ injury, no. 63/045,784, international application no. PCT/US2021/039650). A.A.E.E. has a consulting agreement with TransMedics. F.D.P. is an ad hoc, noncompensated scientific advisor for Medtronic, Abbott, FineHeart and CH Biomedical and a noncompensated medical monitor for Abiomed. F.D.P. is also a member of the data safety monitoring board for Carmat and the NHLBI PumpKIN clinical trial as well as the chair of data safety and management for the DCD heart national FDA clinical trial and the EXPAND heart-Continuous access protocol national FDA trial. P.C.T. is a noncompensated member of the data safety monitoring board for the XVIVO Perfusion PRESERVE trial. The other authors declare no competing interests.

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