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Biology subjects

Mori, M. P.

Publications and source records attributed to Mori, M. P..

2 recordsLinked to original sources

Antiretroviral therapy in the peripartum period impairs post pregnancy cardiac reverse remodeling with early signs of heart failure with preserved ejection fraction

Cardiovascular (CV) disease in pregnancy is the leading cause of maternal mortality worldwide, often associated with the cardiometabolic remodeling needed for fetal growth. In healthy pregnancies these changes reverse postpartum with no consequence, but improper reverse remodeling increases long-term CV risk. Pregnant patients with HIV are at further risk, but it remains unclear whether this is due to chronic low viremia or administration of antiretrovirals (ART). ART used in pregnancy includes nucleoside reverse transcriptase inhibitors (NRTIs), which have known mitochondrial toxicity, and may impact cardiac function. Here, we tested the hypothesis that NRTI-containing ART negatively impacts the maternal heart. Using rats, we show that pregnancy-associated reverse remodeling was impaired by ART. Molecularly, we found mitochondrial changes in the heart and in the liver, leading to dyslipidemia that collectively affected the heart. Our data suggest caution in the choice of ART prescribed for women with HIV during pregnancy and highlight the importance of studies focusing on maternal health.

physiology↗

Mitochondrial membrane potential regulates nuclear DNA methylation and gene expression through phospholipid remodeling

Maintenance of the mitochondrial inner membrane potential ({Delta}{Psi}M) is critical for many aspects of mitochondrial function, including mitochondrial protein import and ion homeostasis. While {Delta}{Psi}M loss and its consequences are well studied, little is known about the effects of increased {Delta}{Psi}M. In this study, we used cells deleted of ATPIF1, a natural inhibitor of the hydrolytic activity of the ATP synthase, as a genetic model of mitochondrial hyperpolarization. Our data show that chronic {Delta}{Psi}M increase leads to nuclear DNA hypermethylation, regulating transcription of mitochondria, carbohydrate and lipid metabolism genes. Surprisingly, remodeling of phospholipids, but not metabolites or redox changes, mechanistically links the {Delta}{Psi}M to the epigenome. These changes were also observed upon chemical exposures and reversed by decreasing the {Delta}{Psi}M, highlighting them as hallmark adaptations to chronic mitochondrial hyperpolarization. Our results reveal the {Delta}{Psi}M as the upstream signal conveying the mitochondrial status to the epigenome to regulate cellular biology, providing a new framework for how mitochondria can influence health outcomes in the absence of canonical dysfunction. HighlightsO_LIMitochondria hyperpolarization leads to nuclear DNA hypermethylation C_LIO_LIDNA methylation regulates expression of mitochondrial and lipid metabolism genes C_LIO_LIPhospholipid remodeling mediates the epigenetic effects of mitochondrial hyperpolarization C_LI

genomics↗