Login / Signup

Cardiac-specific loss of mitoNEET expression is linked with age-related heart failure.

Takaaki FurihataShingo TakadaNaoya KakutaniSatoshi MaekawaMasaya TsudaJunichi MatsumotoWataru MizushimaArata FukushimaTakashi YokotaNobuyuki EnzanShouji MatsushimaHaruka HandaYoshizuki FumotoJunko Nio-KobayashiToshihiko IwanagaShinya TanakaHiroyuki TsutsuiHisataka SabeShintaro Kinugawa
Published in: Communications biology (2021)
Heart failure (HF) occurs frequently among older individuals, and dysfunction of cardiac mitochondria is often observed. We here show the cardiac-specific downregulation of a certain mitochondrial component during the chronological aging of mice, which is detrimental to the heart. MitoNEET is a mitochondrial outer membrane protein, encoded by CDGSH iron sulfur domain 1 (CISD1). Expression of mitoNEET was specifically downregulated in the heart and kidney of chronologically aged mice. Mice with a constitutive cardiac-specific deletion of CISD1 on the C57BL/6J background showed cardiac dysfunction only after 12 months of age and developed HF after 16 months; whereas irregular morphology and higher levels of reactive oxygen species in their cardiac mitochondria were observed at earlier time points. Our results suggest a possible mechanism by which cardiac mitochondria may gradually lose their integrity during natural aging, and shed light on an uncharted molecular basis closely related to age-associated HF.
Keyphrases
  • heart failure
  • left ventricular
  • reactive oxygen species
  • oxidative stress
  • poor prognosis
  • acute heart failure
  • atrial fibrillation
  • metabolic syndrome
  • long non coding rna
  • endoplasmic reticulum