Center of Obesity and Metabolic Diseases, The Third People's Hospital of Chengdu, Chengdu, 610031, China.
Affiliated Hospital of Southwest Jiaotong University, Chengdu, 610036, China.
Theranostics. 2020 Mar 26;10(10):4705-4719. doi: 10.7150/thno.42417. eCollection 2020.
A growing body of evidence has suggested that circular RNAs (circRNAs) are crucial for the regulation of gene expression and their dysregulation is implicated in several diseases. However, the function of circRNAs in obesity remains largely unexplored. : Global changes in the circRNA expression patterns were detected in adipose tissues derived from obese and lean individuals. In particular, circSAMD4A was identified as significantly differentially upregulated and was functionally analyzed, both in vitro and in vivo, using various approaches. : CircSAMD4A overexpression was correlated with a poor prognosis in obese patients. By contrast, circSAMD4A knockdown inhibited differentiation in isolated preadipocytes. In high-fat diet (HFD) -induced obese mice, circSAMD4A knockdown reversed the associated weight gain, reduced food intake, lower body fat, and increased energy expenditure. These mice also exhibited increased insulin sensitivity and glucose tolerance. Furthermore, in vitro experiments indicated that circSAMD4A affected differentiation by binding to miR-138-5p and regulating EZH2 expression. : CircSAMD4A regulated preadipocyte differentiation by acting as a miR-138-5p sponge, and thus increasing EZH2 expression. These results suggested that circSAMD4A can serve as a potential target for obesity treatments and/or as a potential prognostic marker for obese patients following bariatric surgery.
越来越多的证据表明,环状 RNA(circRNAs)在基因表达调控中起着至关重要的作用,它们的失调与多种疾病有关。然而,circRNAs 在肥胖中的功能仍在很大程度上未被探索。
在肥胖和瘦个体的脂肪组织中检测到环状 RNA 表达模式的全局变化。特别是,circSAMD4A 被鉴定为显著差异上调,并通过各种方法在体外和体内进行了功能分析。
circSAMD4A 的过表达与肥胖患者的不良预后相关。相比之下,circSAMD4A 的敲低抑制了分离的前体脂肪细胞的分化。在高脂肪饮食(HFD)诱导的肥胖小鼠中,circSAMD4A 的敲低逆转了相关的体重增加,减少了食物摄入,降低了体脂肪,并增加了能量消耗。这些小鼠还表现出更高的胰岛素敏感性和葡萄糖耐量。此外,体外实验表明,circSAMD4A 通过与 miR-138-5p 结合并调节 EZH2 表达来影响分化。
circSAMD4A 通过作为 miR-138-5p 的海绵来调节前体脂肪细胞分化,从而增加 EZH2 的表达。这些结果表明,circSAMD4A 可以作为肥胖治疗的潜在靶点,或作为肥胖患者接受减肥手术后的潜在预后标志物。