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

Authors :
Furihata, Takaaki
Takada, Shingo
Kakutani, Naoya
Maekawa, Satoshi
Tsuda, Masaya
Matsumoto, Junichi
Mizushima, Wataru
Fukushima, Arata
Yokota, Takashi
Enzan, Nobuyuki
Matsushima, Shouji
Handa, Haruka
Fumoto, Yoshizuki
Nio-Kobayashi, Junko
Iwanaga, Toshihiko
Tanaka, Shinya
Tsutsui, Hiroyuki
Sabe, Hisataka
Kinugawa, Shintaro
Source :
Communications Biology; 1/29/2021, Vol. 4 Issue 1, p1-11, 11p
Publication Year :
2021

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. Takaaki Furihata et al. report a new mouse model with heart-specific deletion of the mitochondrial protein, mitoNEET. Their results suggest that loss of mitoNEET expression may contribute to age-associated heart failure in older adults. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
23993642
Volume :
4
Issue :
1
Database :
Complementary Index
Journal :
Communications Biology
Publication Type :
Academic Journal
Accession number :
148405713
Full Text :
https://doi.org/10.1038/s42003-021-01675-4