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

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作者
Takaaki Furihata
Shingo Takada
Naoya Kakutani
Satoshi Maekawa
Masaya Tsuda
Junichi Matsumoto
Wataru Mizushima
Arata Fukushima
Takashi Yokota
Nobuyuki Enzan
Shouji Matsushima
Haruka Handa
Yoshizuki Fumoto
Junko Nio-Kobayashi
Toshihiko Iwanaga
Shinya Tanaka
Hiroyuki Tsutsui
Hisataka Sabe
Shintaro Kinugawa
机构
[1] Hokkaido University,Department of Cardiovascular Medicine, Faculty of Medicine and Graduate School of Medicine
[2] Kyushu University Graduate School of Medical Sciences,Department of Cardiovascular Medicine
[3] Hokkaido University,Department of Molecular Biology, Faculty of Medicine and Graduate School of Medicine
[4] Hokkaido University,Laboratory of Histology and Cytology, Department of Anatomy, Faculty of Medicine and Graduate School of Medicine
[5] Hokkaido University,Department of Cancer Pathology, Faculty of Medicine and Graduate School of Medicine
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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.
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