Sex differences and altered mitophagy in experimental pulmonary hypertension

Abstract

Pulmonary hypertension (PH) is a debilitating condition characterized by increased pulmonary arterial pressures and remodeling of pulmonary arteries, leading to right heart failure. Women have a higher prevalence of PH, whereas men have more severe disease and poorer outcomes. Animal models also show female-predominant disease. Despite the known sex differences in PH, little is known about how pathogenesis differs between the sexes. There is growing evidence of mitochondrial dysfunction, as well as altered mitophagy in PH. We hypothesized that sexual dimorphism contributes to mitochondrial dysfunction and altered mitophagy in PH. Using mouse lung endothelial cells, we exposed both wild-type and Parkin−/− cells to hypoxia and measured the effects on mitochondrial function and mitophagy-associated proteins. Our results show that females have more Parkin expression at baseline as well as increased mitochondrial respiratory capacity when exposed to oxidative stress. Inhibition of Parkin increased metabolic activity but reduced cell proliferation but to different degrees depending on sex, with results differing by sex. Our findings demonstrate sexual dimorphism in mitophagy-associated proteins and in mitochondrial respiration, which may help shed light on how the pathogenesis of PH may differ between the sexes.

Document Details

Document Type
Pub Defense Publication
Publication Date
May 01, 2022
Source ID
10.1152/ajplung.00019.2020

Entities

People

  • Isabel S. Bazan
  • Maor Sauler
  • Patty J Lee
  • Peiying Shan
  • So-jin Kim
  • Taylor A. Ardito
  • Yi Zhang

Organizations

  • Biomedical Laboratory Research and Development, VA Office of Research and Development
  • Duke University
  • National Heart, Lung, and Blood Institute
  • United States Department of Defense
  • Yale School of Medicine

Tags

Fields of Study

  • Biology
  • Medicine

Readers

  • Cardiovascular Physiology
  • Gender and Food Studies
  • Gulf War Illness and Chronic Multisymptom Illness in Veterans.