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腺病毒在肥胖中的作用。

Role of adenoviruses in obesity.

机构信息

Epidemiology Consult Division, United States Air Force School of Aerospace Medicine, Wright-Patterson AFB, OH, USA.

Virginia Obesity Research Institute, Richmond, VA, USA.

出版信息

Rev Med Virol. 2015 Nov;25(6):379-87. doi: 10.1002/rmv.1852. Epub 2015 Sep 9.

Abstract

UNLABELLED

Five human adenovirus subtypes, Ad5, Ad9, Ad31, Ad36, and Ad37, and a non-human adenovirus, SMAM1, are linked to increased adiposity in vitro or in vivo. Experimental infection with Ad5, Ad36, and Ad37 produced excess adiposity or weight gain in animals. Ad9 and Ad31 increase fat storage in tissue culture but are not associated with animal or human obesity. Ad36 is the most extensively studied adipogenic adenovirus and is correlated with some measure of overweight/obesity in humans from multiple countries. The correlation is strongest and most consistent in children, but some studies have been negative in both children and adults. About 30% of overweight/obese children and adults and about 15-20% of lean individuals have Ad36 antibodies in epidemiologic studies. The mechanisms of action of Ad36 are due to the early gene 4, open reading frame 1 (E4-ORF1). Blocking E4-ORF1 with siRNA prevents the effects of Ad36, and transfection of lentivirus with E4-ORF1 reproduces the Ad36 effects. Increased adiposity is caused by stimulation of at least three pathways by Ad36. Cell membrane glucose receptors are increased via the Ras pathway, leading to increased intracellular glucose. Fatty acid synthase is increased, which converts the glucose to fatty acids. Finally, peroxisome proliferator-activated receptor-γ is increased, resulting in differentiation of adult stem cells into adipocytes.

CONCLUSIONS

several adenoviruses increase adiposity in animals and are associated with obesity in humans. There are critical gaps in the literature needing further investigation including evaluation of other adenovirus subtypes and better research designs to improve the strength of causal inferences.

摘要

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五种人类腺病毒亚型(Ad5、Ad9、Ad31、Ad36 和 Ad37)和一种非人类腺病毒 SMAM1,与体外或体内脂肪增加有关。实验性感染 Ad5、Ad36 和 Ad37 会导致动物肥胖或体重增加。Ad9 和 Ad31 在组织培养中增加脂肪储存,但与动物或人类肥胖无关。Ad36 是研究最广泛的致脂肪腺病毒,与来自多个国家的一些超重/肥胖人类指标相关。这种相关性在儿童中最强且最一致,但一些研究在儿童和成人中均为阴性。在流行病学研究中,约 30%的超重/肥胖儿童和成人以及约 15-20%的瘦人有 Ad36 抗体。Ad36 的作用机制归因于早期基因 4、开放阅读框 1(E4-ORF1)。用 siRNA 阻断 E4-ORF1 可阻止 Ad36 的作用,而用 E4-ORF1 转染慢病毒可再现 Ad36 的作用。Ad36 通过至少三条途径刺激脂肪增加。细胞膜葡萄糖受体通过 Ras 途径增加,导致细胞内葡萄糖增加。脂肪酸合酶增加,将葡萄糖转化为脂肪酸。最后,过氧化物酶体增殖物激活受体-γ 增加,导致成人干细胞分化为脂肪细胞。

结论

几种腺病毒会使动物肥胖,并与人类肥胖有关。文献中有一些关键的空白需要进一步研究,包括评估其他腺病毒亚型和更好的研究设计,以提高因果推断的强度。

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