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The functional role of Higd1a in mitochondrial homeostasis and in multiple disease processes.

作者信息

Zhu Jie-Ying, Chen Min, Mu Wang-Jing, Luo Hong-Yang, Guo Liang

机构信息

School of Kinesiology, Shanghai University of Sport, Shanghai 200438, China.

Shanghai Frontiers Science Research Base of Exercise and Metabolic Health, Shanghai University of Sport, Shanghai 200438, China.

出版信息

Genes Dis. 2022 Apr 22;10(5):1833-1845. doi: 10.1016/j.gendis.2022.03.018. eCollection 2023 Sep.


DOI:10.1016/j.gendis.2022.03.018
PMID:37492734
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10363561/
Abstract

is a conserved gene in evolution which is widely expressed in many tissues in mammals. Accumulating evidence has revealed multiple functions of Higd1a, as a mitochondrial inner membrane protein, in the regulation of metabolic homeostasis. It plays an important role in anti-apoptosis and promotes cellular survival in several cell types under hypoxic condition. And the survival of porcine Sertoli cells facilitated by Higd1a helps to support reproduction. In some cases, Higd1a can serve as a sign of metabolic stress. Over the past several years, a considerable amount of studies about how tumor fate is determined and how cancerous proliferation is regulated by Higd1a have been performed. In this review, we summarize the physiological functions of Higd1a in metabolic homeostasis and its pathophysiological roles in distinct diseases including cancer, nonalcoholic fatty liver disease (NAFLD), type II diabetes and mitochondrial diseases. The prospect of Higd1a with potential to preserve mammal health is also discussed. This review might pave the way for Higd1a-based research and application in clinical practice.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe3/10363561/266ef3ee373c/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe3/10363561/5be9ab989443/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe3/10363561/7ce4cbd80754/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe3/10363561/d885c6d4d939/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe3/10363561/de79db2a2aa6/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe3/10363561/266ef3ee373c/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe3/10363561/5be9ab989443/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe3/10363561/7ce4cbd80754/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe3/10363561/d885c6d4d939/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe3/10363561/de79db2a2aa6/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe3/10363561/266ef3ee373c/gr5.jpg

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The functional role of Higd1a in mitochondrial homeostasis and in multiple disease processes.

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[2]
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[10]
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本文引用的文献

[1]
Cysteine dioxygenase type 1 (CDO1): Its functional role in physiological and pathophysiological processes.

Genes Dis. 2022-2-17

[2]
SERPINA3C ameliorates adipose tissue inflammation through the Cathepsin G/Integrin/AKT pathway.

Mol Metab. 2022-7

[3]
Exercise-Mediated Browning of White Adipose Tissue: Its Significance, Mechanism and Effectiveness.

Int J Mol Sci. 2021-10-26

[4]
l-Theanine Activates the Browning of White Adipose Tissue Through the AMPK/α-Ketoglutarate/Prdm16 Axis and Ameliorates Diet-Induced Obesity in Mice.

Diabetes. 2021-7

[5]
Global epidemiology of NAFLD-related HCC: trends, predictions, risk factors and prevention.

Nat Rev Gastroenterol Hepatol. 2021-4

[6]
Mitochondrial Dynamics: Fission and Fusion in Fate Determination of Mesenchymal Stem Cells.

Front Cell Dev Biol. 2020-10-15

[7]
Cytochrome c oxidase deficiency.

Biochim Biophys Acta Bioenerg. 2021-1-1

[8]
Mitochondria and Calcium in Alzheimer's Disease: From Cell Signaling to Neuronal Cell Death.

Trends Neurosci. 2021-2

[9]
Mitochondrial disorders of the OXPHOS system.

FEBS Lett. 2021-4

[10]
Defective mitophagy in Alzheimer's disease.

Ageing Res Rev. 2020-10-3

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