Center of Excellence in Translational Medicine, CEMT-BIOREN, Universidad de La Frontera, Temuco, Chile.
Department of Internal Medicine, Universidad de La Frontera, Temuco, Chile.
Int J Obes (Lond). 2024 Oct;48(10):1414-1420. doi: 10.1038/s41366-024-01555-x. Epub 2024 Jun 19.
Human Adenovirus D-36 (HAdV-D36) promotes adipogenesis in cellular and animal models and may contribute to the development of human obesity. Induction of PPARγ by HAdV-D36 seems to have a central role in the maintenance of adipogenic status. There is limited information about epigenetic mechanisms contributing to this process in human adipose tissue. This study evaluated the expression of lncRNAs (ADINR, GAS5 and MEG3) and miRNAs (miR-18a and miR-140) involved in the adipogenic process in visceral adipose tissue (VAT) of subjects with obesity with previous HAdV-D36 infection (seropositive) and unexposed (seronegative) subjects with obesity.
Individuals with obesity were grouped according to the presence of antibodies against HAdV-D36 (Seropositive: HAdV-D36[+], n = 29; and Seronegative: HAdV-D36[-], n = 28). Additionally, a group of individuals without obesity (n = 17) was selected as a control group. The HAdV-D36 serology was carried out by ELISA. Biopsies of VAT were obtained during an elective and clinically indicated surgery (bariatric or cholecystectomy). RNA extraction from VAT was performed and the expression of PPARG and non-coding RNAs was evaluated by qPCR.
HAdV-D36[+] individuals had lower expression of anti-adipogenic lncRNAs GAS5 (p = 0.016) and MEG3 (p = 0.035) compared with HAdV-D36[-] subjects with obesity. HAdV-D36[+] subjects also presented increased expression of the adipogenic miRNA miR-18a (p = 0.042), which has been reported to be modulated by GAS5 through a RNA sponging mechanism during adipogenic differentiation. Additionally, an inverse correlation of GAS5 with PPARG expression was observed (r = -0.917, p = 0.01).
Our results suggest that HAdV-D36 is related to non-coding RNAs implicated in adipogenesis, representing a potential mechanism by which previous HAdV-D36 infection could be associated with the long-term maintenance of adipogenic status, probably through the GAS5/miR-18a axis.
人类腺病毒 D-36(HAdV-D36)在细胞和动物模型中促进脂肪生成,可能导致人类肥胖的发生。HAdV-D36 诱导 PPARγ 的表达似乎在维持脂肪生成状态方面起着核心作用。关于表观遗传机制在人类脂肪组织中对这一过程的贡献,信息有限。本研究评估了内脏脂肪组织(VAT)中涉及脂肪生成过程的 lncRNA(ADINR、GAS5 和 MEG3)和 miRNA(miR-18a 和 miR-140)的表达,这些组织来自于先前感染 HAdV-D36(血清阳性)和未暴露(血清阴性)的肥胖个体。
根据是否存在针对 HAdV-D36 的抗体,将肥胖个体分为血清阳性(HAdV-D36[+],n=29)和血清阴性(HAdV-D36[-],n=28)组。此外,还选择了一组不肥胖的个体(n=17)作为对照组。通过 ELISA 进行 HAdV-D36 血清学检测。在择期和临床需要的手术(减肥或胆囊切除术)中获取 VAT 活检。从 VAT 中提取 RNA,并通过 qPCR 评估 PPARG 和非编码 RNA 的表达。
与肥胖的 HAdV-D36[-]个体相比,HAdV-D36[+]个体的抗脂肪生成 lncRNA GAS5(p=0.016)和 MEG3(p=0.035)表达水平较低。HAdV-D36[+]个体的脂肪生成 miRNA miR-18a 表达也增加(p=0.042),据报道,在脂肪生成分化过程中,miR-18a 可以通过 GAS5 的 RNA 海绵机制进行调节。此外,还观察到 GAS5 与 PPARG 表达呈负相关(r=-0.917,p=0.01)。
我们的结果表明,HAdV-D36 与参与脂肪生成的非编码 RNA 有关,这代表了先前 HAdV-D36 感染与脂肪生成状态的长期维持相关的潜在机制,可能通过 GAS5/miR-18a 轴。