Rathod M, Vangipuram S D, Krishnan B, Heydari A R, Holland T C, Dhurandhar N V
Department of Nutrition and Food Science, Detroit, Michigan, USA.
Int J Obes (Lond). 2007 Jan;31(1):78-86. doi: 10.1038/sj.ijo.0803358. Epub 2006 May 2.
Human adenovirus Ad-36 causes adiposity in animal models and shows association with human obesity. Ad-36 enhances differentiation of 3T3-L1 and human preadipocytes, without cell lysis, a characteristic that may contribute to its adipogenic effect observed in vivo. Ad-2, another human adenovirus is nonadipogenic in animals and in 3T3-L1 cells and shows no correlation with human obesity. The objective of this study was to determine the adipogenic roles of viral mRNA and DNA, which may explain the differential effects of Ad-36 and Ad-2 on preadipocyte differentiation.
This study determined the duration of selected Ad-36 gene expression in 3T3-L1 cells, and the effect on preadipocytes differentiation, when Ad-36 gene expression was attenuated by Cidofovir, an antiadenoviral agent.
The results showed that Ad-36, but not Ad-2, expresses viral mRNA. Ad-36 gene expression peaked at 2-4 days postinoculation and very low levels persisted after day 7. Despite the viral mRNA expression, Ad-36 infection of 3T3-L1 cells was abortive as indicated by a progressive decrease in viral DNA quantity. Attenuation of Ad-36 mRNA expression by Cidofovir reduced the adipogenic effect of the virus.
In conclusion, viral mRNA expression, although transient, is a prerequisite for enhancing differentiation of preadipocytes by Ad-36. Viral DNA replication was not required for the effect. This is the first evidence for the role of gene expression of an adipogenic human virus in enhancing preadipocytes differentiation. This study provides the basis for further understanding novel regulatory modulators of preadipocytes differentiation.
人腺病毒Ad - 36在动物模型中可导致肥胖,且与人类肥胖相关。Ad - 36可促进3T3 - L1细胞和人脂肪前体细胞的分化,且不会引起细胞裂解,这一特性可能有助于其在体内产生致肥胖效应。另一种人腺病毒Ad - 2在动物和3T3 - L1细胞中不具有致肥胖性,且与人类肥胖无相关性。本研究的目的是确定病毒mRNA和DNA在脂肪生成中的作用,这可能解释Ad - 36和Ad - 2对脂肪前体细胞分化的不同影响。
本研究确定了3T3 - L1细胞中选定的Ad - 36基因表达持续时间,以及当用抗腺病毒药物西多福韦减弱Ad - 36基因表达时对脂肪前体细胞分化的影响。
结果显示,Ad - 36可表达病毒mRNA,而Ad - 2则不能。Ad - 36基因表达在接种后2 - 4天达到峰值,7天后仍维持在很低水平。尽管有病毒mRNA表达,但3T3 - L1细胞被Ad - 36感染是流产性的,这可通过病毒DNA数量的逐渐减少来表明。西多福韦减弱Ad - 36 mRNA表达可降低该病毒的致肥胖效应。
总之,病毒mRNA表达虽短暂,但却是Ad - 36增强脂肪前体细胞分化的先决条件。该效应不需要病毒DNA复制。这是关于致肥胖人病毒的基因表达在增强脂肪前体细胞分化中作用的首个证据。本研究为进一步理解脂肪前体细胞分化的新型调节因子提供了基础。