| Literature DB >> 33514783 |
Takaaki Furihata1, Shingo Takada1, Naoya Kakutani1, Satoshi Maekawa1, Masaya Tsuda1, Junichi Matsumoto1, Wataru Mizushima1, Arata Fukushima1, Takashi Yokota1, Nobuyuki Enzan2, Shouji Matsushima2, Haruka Handa3, Yoshizuki Fumoto3, Junko Nio-Kobayashi4, Toshihiko Iwanaga4, Shinya Tanaka5, Hiroyuki Tsutsui2, Hisataka Sabe3, Shintaro Kinugawa6.
Abstract
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.Entities:
Year: 2021 PMID: 33514783 PMCID: PMC7846856 DOI: 10.1038/s42003-021-01675-4
Source DB: PubMed Journal: Commun Biol ISSN: 2399-3642