Muscle RING finger-1 promotes a maladaptive phenotype in chronic hypoxia-induced right ventricular remodeling

Matthew J. Campen, Michael L. Paffett, E. Sage Colombo, Selita N. Lucas, Tamara Anderson, Monique Nysus, Jeffrey P. Norenberg, Ben Gershman, Jacob Hesterman, Jack Hoppin, Monte Willis

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Exposure to chronic hypoxia (CH) induces elevated pulmonary artery pressure/resistance, leading to an eventual maladaptive right ventricular hypertrophy (RVH). Muscle RING finger-1 (MuRF1) is a muscle-specific ubiquitin ligase that mediates myocyte atrophy and has been shown to play a role in left ventricular hypertrophy and altered cardiac bioenergetics in pressure overloaded hearts. However, little is known about the contribution of MuRF1 impacting RVH in the setting of CH. Therefore, we hypothesized that MuRF1 deletion would enhance RVH compared to their wild-type littermates, while cardiac-specific overexpression would reduce hypertrophy following CH-induced pulmonary hypertension. We assessed right ventricular systolic pressure (RVSP), right ventricle to left ventricle plus septal weight ratio (RV/LV+S) and hematocrit (Hct) following a 3-wk isobaric CH exposure. Additionally, we conducted dual-isotope SPECT/CT imaging with cardiac function agent 201Tl- chloride and cell death agent 99mTc-annexin V. Predictably, CH induced pulmonary hypertension, measured by increased RVSP, RV/LV+S and Hct in WT mice compared to normoxic WT mice. Normoxic WT and MuRF1-null mice exhibited no significant differences in RVSP, RV/LV+S or Hct. CH-induced increases in RVSP were also similar between WT and MuRF1-null mice; however, RV/LV+S and Hct were significantly elevated in CH-exposed MuRF1-null mice compared to WT. In cardiac-specific MuRF1 overexpressing mice, RV/LV+S increased significantly due to CH exposure, even greater than in WT mice. This remodeling appeared eccentric, maladaptive and led to reduced systemic perfusion. In conclusion, these results are consistent with an atrophic role for MuRF1 regulating the magnitude of right ventricular hypertrophy following CH-induction of pulmonary hypertension.

Original languageEnglish (US)
Article numbere97084
JournalPLoS ONE
Volume9
Issue number5
DOIs
StatePublished - May 8 2014
Externally publishedYes

Fingerprint

Ventricular Remodeling
Muscle
hypoxia
Phenotype
hypertrophy
phenotype
Muscles
muscles
Right Ventricular Hypertrophy
Ventricular Pressure
Hematocrit
mice
hematocrit
Pulmonary Hypertension
hypertension
Blood Pressure
lungs
Heart Ventricles
Hypoxia
Pressure

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Agricultural and Biological Sciences(all)

Cite this

Muscle RING finger-1 promotes a maladaptive phenotype in chronic hypoxia-induced right ventricular remodeling. / Campen, Matthew J.; Paffett, Michael L.; Colombo, E. Sage; Lucas, Selita N.; Anderson, Tamara; Nysus, Monique; Norenberg, Jeffrey P.; Gershman, Ben; Hesterman, Jacob; Hoppin, Jack; Willis, Monte.

In: PLoS ONE, Vol. 9, No. 5, e97084, 08.05.2014.

Research output: Contribution to journalArticle

Campen, MJ, Paffett, ML, Colombo, ES, Lucas, SN, Anderson, T, Nysus, M, Norenberg, JP, Gershman, B, Hesterman, J, Hoppin, J & Willis, M 2014, 'Muscle RING finger-1 promotes a maladaptive phenotype in chronic hypoxia-induced right ventricular remodeling', PLoS ONE, vol. 9, no. 5, e97084. https://doi.org/10.1371/journal.pone.0097084
Campen, Matthew J. ; Paffett, Michael L. ; Colombo, E. Sage ; Lucas, Selita N. ; Anderson, Tamara ; Nysus, Monique ; Norenberg, Jeffrey P. ; Gershman, Ben ; Hesterman, Jacob ; Hoppin, Jack ; Willis, Monte. / Muscle RING finger-1 promotes a maladaptive phenotype in chronic hypoxia-induced right ventricular remodeling. In: PLoS ONE. 2014 ; Vol. 9, No. 5.
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