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Difference between revisions of "Zhao 2021 Diabetes"

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(Created page with "{{Publication |title=Zhao Q, Luo T, Gao F, Fu Y, Li B, Shao X, Chen H, Zhou Z, Guo S, Shen L, Jin L, Cen D, Zhou H, Lyu J, Fang H (2021) GRP75 regulates mitochondrial-supercom...")
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{{Publication
{{Publication
|title=Zhao Q, Luo T, Gao F, Fu Y, Li B, Shao X, Chen H, Zhou Z, Guo S, Shen L, Jin L, Cen D, Zhou H, Lyu J, Fang H (2021) GRP75 regulates mitochondrial-supercomplex turnover to modulate insulin sensitivity. Diabetes [Epub ahead of print].
|title=Zhao Q, Luo T, Gao F, Fu Y, Li B, Shao X, Chen H, Zhou Z, Guo S, Shen L, Jin L, Cen D, Zhou H, Lyu J, Fang H (2021) GRP75 regulates mitochondrial-supercomplex turnover to modulate insulin sensitivity. Diabetes 71:233-48.
|info=[https://www.ncbi.nlm.nih.gov/pubmed/34810178 PMID: 34810178 Open Access]
|info=[https://www.ncbi.nlm.nih.gov/pubmed/34810178 PMID: 34810178]
|authors=Zhao Q, Luo T, Gao F, Fu Y, Li B, Shao X, Chen H, Zhou Z, Guo S, Shen L, Jin L, Cen D, Zhou H, Lyu J, Fang H
|authors=Zhao Qiongya, Luo Ting, Gao Feng, Fu Yinxu, Li Bin, Shao Xiaoli, Chen Haifeng, Zhou Zhuohua, Guo Sihan, Shen Lijun, Jin Liqin, Cen Dong, Zhou Huaibin, Lyu Jianxin, Fang Hezhi
|year=2021
|year=2021
|journal=Diabetes
|journal=Diabetes
|abstract=GRP75, defined as a major component of both mitochondrial quality control system and mitochondria-associated membrane, plays a key role in mitochondrial homeostasis. In this study, we assessed the roles of GRP75, other than as a component, in insulin action in both in vitro and in vivo models with insulin resistance. We found that GRP75 was downregulated in HFD-fed mice, and induction of Grp75 in mice could prevent HFD induced obesity and insulin resistance. Mechanistically, GRP75 influenced insulin sensitivity by regulating mitochondrial function through its modulation of mitochondrial-supercomplex turnover rather than MAM communication: GRP75 was negatively associated with respiratory-chain complex activity and was essential for mitochondrial-supercomplex assembly and stabilization. Moreover, mitochondrial dysfunction in Grp75-knockdown cells might further increase mitochondrial fragmentation, thus trigger cytosolic mitochondrial DNA release and activate the cGAS/STING-dependent pro-inflammatory response. Therefore, GRP75 can serve as a potential therapeutic target of insulin resistant-related diabetes or other metabolic diseases.
|abstract=GRP75, defined as a major component of both mitochondrial quality control system and mitochondria-associated membrane, plays a key role in mitochondrial homeostasis. In this study, we assessed the roles of GRP75, other than as a component, in insulin action in both ''in vitro'' and ''in vivo'' models with insulin resistance. We found that GRP75 was downregulated in HFD-fed mice, and induction of Grp75 in mice could prevent HFD induced obesity and insulin resistance. Mechanistically, GRP75 influenced insulin sensitivity by regulating mitochondrial function through its modulation of mitochondrial-supercomplex turnover rather than MAM communication: GRP75 was negatively associated with respiratory-chain complex activity and was essential for mitochondrial-supercomplex assembly and stabilization. Moreover, mitochondrial dysfunction in Grp75-knockdown cells might further increase mitochondrial fragmentation, thus trigger cytosolic mitochondrial DNA release and activate the cGAS/STING-dependent pro-inflammatory response. Therefore, GRP75 can serve as a potential therapeutic target of insulin resistant-related diabetes or other metabolic diseases.
|editor=[[Plangger M]]
|editor=[[Plangger M]]
}}
}}
{{Labeling
{{Labeling
|area=Respiration
|area=Respiration
|diseases=Diabetes
|organism=Human, Mouse
|enzymes=Supercomplex
|instruments=Oxygraph-2k
|instruments=Oxygraph-2k
|additional=2021-11
|additional=CN, 2021-11
}}
}}

Latest revision as of 03:32, 21 November 2023

Publications in the MiPMap
Zhao Q, Luo T, Gao F, Fu Y, Li B, Shao X, Chen H, Zhou Z, Guo S, Shen L, Jin L, Cen D, Zhou H, Lyu J, Fang H (2021) GRP75 regulates mitochondrial-supercomplex turnover to modulate insulin sensitivity. Diabetes 71:233-48.

Β» PMID: 34810178

Zhao Qiongya, Luo Ting, Gao Feng, Fu Yinxu, Li Bin, Shao Xiaoli, Chen Haifeng, Zhou Zhuohua, Guo Sihan, Shen Lijun, Jin Liqin, Cen Dong, Zhou Huaibin, Lyu Jianxin, Fang Hezhi (2021) Diabetes

Abstract: GRP75, defined as a major component of both mitochondrial quality control system and mitochondria-associated membrane, plays a key role in mitochondrial homeostasis. In this study, we assessed the roles of GRP75, other than as a component, in insulin action in both in vitro and in vivo models with insulin resistance. We found that GRP75 was downregulated in HFD-fed mice, and induction of Grp75 in mice could prevent HFD induced obesity and insulin resistance. Mechanistically, GRP75 influenced insulin sensitivity by regulating mitochondrial function through its modulation of mitochondrial-supercomplex turnover rather than MAM communication: GRP75 was negatively associated with respiratory-chain complex activity and was essential for mitochondrial-supercomplex assembly and stabilization. Moreover, mitochondrial dysfunction in Grp75-knockdown cells might further increase mitochondrial fragmentation, thus trigger cytosolic mitochondrial DNA release and activate the cGAS/STING-dependent pro-inflammatory response. Therefore, GRP75 can serve as a potential therapeutic target of insulin resistant-related diabetes or other metabolic diseases.

β€’ Bioblast editor: Plangger M


Labels: MiParea: Respiration  Pathology: Diabetes 

Organism: Human, Mouse 


Enzyme: Supercomplex 


HRR: Oxygraph-2k 

CN, 2021-11