Role of hypoxia-inducible factors in regulating right ventricular function and remodeling during chronic hypoxia–induced pulmonary hypertension

Kimberly A. Smith, Gregory B. Waypa, V. Joseph Dudley, G. R. Scott Budinger, Hiam Abdala-Valencia, Elizabeth Bartom, Paul T. Schumacker*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

Pulmonary hypertension (PH) and right ventricular (RV) hypertrophy frequently develop in patients with hypoxic lung disease. Chronic alveolar hypoxia (CH) promotes sustained pulmonary vasoconstriction and pulmonary artery (PA) remodeling by acting on lung cells, resulting in the development of PH. RV hypertrophy develops in response to PH, but coronary arterial hypoxemia in CH may influence that response by activating HIF-1a (hypoxia-inducible factor 1a) and/or HIF-2a in cardiomyocytes. Indeed, other studies show that the attenuation of PH in CH fails to prevent RV remodeling, suggesting that PH-independent factors regulate RV hypertrophy. Therefore, we examined the role of HIFs in RV remodeling in CH-induced PH. We deleted HIF-1a and/or HIF-2a in hearts of adult mice that were then housed under normoxia or CH (10% O2) for 4 weeks. RNA-sequencing analysis of the RV revealed that HIF-1a and HIF-2a regulate the transcription of largely distinct gene sets during CH. RV systolic pressure increased, and RV hypertrophy developed in CH. The deletion of HIF-1a in smooth muscle attenuated the CH-induced increases in RV systolic pressure but did not decrease hypertrophy. The deletion of HIF-1a in cardiomyocytes amplified RV remodeling; this was abrogated by the simultaneous loss of HIF-2a. CH decreased stroke volume and cardiac output in wild-type but not in HIF-1a–deficient hearts, suggesting that CH may cause cardiac dysfunction via HIF-dependent signaling. Collectively, these data reveal that HIF-1 and HIF-2 act together in RV cardiomyocytes to orchestrate RV remodeling in CH, with HIF-1 playing a protective role rather than driving hypertrophy.

Original languageEnglish (US)
Pages (from-to)652-664
Number of pages13
JournalAmerican journal of respiratory cell and molecular biology
Volume63
Issue number5
DOIs
StatePublished - Nov 2020

Keywords

  • Hypoxia
  • Hypoxia-inducible factors
  • Right ventricular hypertrophy

ASJC Scopus subject areas

  • Molecular Biology
  • Pulmonary and Respiratory Medicine
  • Clinical Biochemistry
  • Cell Biology

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