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INDY——动物和人类代谢调节的新纽带。

INDY-A New Link to Metabolic Regulation in Animals and Humans.

作者信息

Rogina Blanka

机构信息

Department of Genetics and Genome Sciences, Institute for Systems Genomics, School of Medicine, University of Connecticut Health Center, FarmingtonCT, United States.

出版信息

Front Genet. 2017 May 24;8:66. doi: 10.3389/fgene.2017.00066. eCollection 2017.

Abstract

The () gene encodes the fly homolog of the mammalian SLC13A5 citrate transporter. Reduced expression of the gene in flies and worms extends their longevity. INDY is expressed in the plasma membrane of metabolically active tissues. Decreased expression of in worms, flies, mice, and rats alters metabolism in a manner similar to calorie restriction. Reducing INDY activity prevents weight gain in flies, worms, and mice, and counteracts the negative effects of age or a high fat diet on metabolism and insulin sensitivity. The metabolic effects of reducing INDY activity are the result of reduced cytoplasmic citrate. Citrate is a key metabolite and has a central role in energy status of the cell by effecting lipid and carbohydrate metabolism and energy production. Thereby newly described drugs that reduce INDY transporting activity increase insulin sensitivity and reduce hepatic lipid levels via its effect on hepatic citrate uptake. A recent report presented the first direct link between increased hepatic levels of human INDY, insulin resistance, and non-alcoholic fatty liver disease in obese humans. Similarly increased hepatic levels were observed in non-human primates fed on a high fat diet for 2 years. This effect is mediated via the stimulatory effect of the interleukin-6/Stat3 pathway on mINDY hepatic expression. These findings make INDY a potential and very promising target for the treatment of metabolic disorders in humans.

摘要

()基因编码哺乳动物SLC13A5柠檬酸转运蛋白的果蝇同源物。果蝇和蠕虫中该基因表达的降低可延长其寿命。INDY在代谢活跃组织的质膜中表达。蠕虫、果蝇、小鼠和大鼠中该基因表达的降低以类似于热量限制的方式改变新陈代谢。降低INDY活性可防止果蝇、蠕虫和小鼠体重增加,并抵消年龄或高脂肪饮食对新陈代谢和胰岛素敏感性的负面影响。降低INDY活性的代谢作用是细胞质柠檬酸减少的结果。柠檬酸是一种关键代谢物,通过影响脂质和碳水化合物代谢以及能量产生,在细胞能量状态中起核心作用。因此,新描述的降低INDY转运活性的药物通过影响肝脏对柠檬酸的摄取,增加胰岛素敏感性并降低肝脏脂质水平。最近的一份报告首次揭示了肥胖人群肝脏中人类INDY水平升高、胰岛素抵抗和非酒精性脂肪肝病之间的直接联系。同样,在喂食高脂肪饮食两年的非人类灵长类动物中也观察到肝脏INDY水平升高。这种效应是通过白细胞介素-6/Stat3途径对肝脏mINDY表达的刺激作用介导的。这些发现使INDY成为治疗人类代谢紊乱的一个潜在且非常有前景的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd25/5442177/d95131d5d22f/fgene-08-00066-g001.jpg

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本文引用的文献

1
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The human longevity gene homolog INDY and interleukin-6 interact in hepatic lipid metabolism.
Hepatology. 2017 Aug;66(2):616-630. doi: 10.1002/hep.29089. Epub 2017 Jun 26.
3
Punctate white matter lesions in full-term infants with neonatal seizures associated with SLC13A5 mutations.
Eur J Paediatr Neurol. 2017 Mar;21(2):396-403. doi: 10.1016/j.ejpn.2016.11.002. Epub 2016 Nov 19.
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Optimization of a Dicarboxylic Series for in Vivo Inhibition of Citrate Transport by the Solute Carrier 13 (SLC13) Family.
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Knockdown of Indy/CeNac2 extends Caenorhabditis elegans life span by inducing AMPK/aak-2.
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