Xu Lu-lian, Shi Chun-mei, Xu Guang-feng, Chen Ling, Zhu Ling-ling, Zhu Lu, Guo Xi-rong, Xu Mei-yu, Ji Chen-bo
Department of Pediatrics, Affiliated Hospital of Nantong University, Nantong, 226000, People's Republic of China.
Cell Biochem Biophys. 2014 Nov;70(2):771-6. doi: 10.1007/s12013-014-9980-x.
Obesity has become a global public health problem associated with complications including type 2 diabetes, cardiovascular disease, and several cancers. Adipocyte differentiation (adipogenesis) plays an important role in obesity and energy homeostasis. Adipose tissue secretes multiple cytokines and adipokines which can cause the complications of obesity, especially insulin resistance. TNF-α, IL-6, leptin, and resistin have been identified as the main regulators of obesity and insulin activity. miR-378 is highly induced during adipogenesis and has been reported to be positively regulated in adipogenesis. In the current study, matured human adipocytes were treated with TNF-α, IL-6, leptin, or resistin on the 15th day after the induction of human pre-adipocyte differentiation. We demonstrated that TNF-α, IL-6, and leptin upregulated miR-378 expression indicating that miR-378 probably is a novel mediator in the development of insulin resistance related to obesity.
肥胖已成为一个全球性的公共卫生问题,与包括2型糖尿病、心血管疾病和几种癌症在内的并发症相关。脂肪细胞分化(脂肪生成)在肥胖和能量稳态中起重要作用。脂肪组织分泌多种细胞因子和脂肪因子,它们可导致肥胖并发症,尤其是胰岛素抵抗。肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)、瘦素和抵抗素已被确定为肥胖和胰岛素活性的主要调节因子。miR-378在脂肪生成过程中被高度诱导,并且据报道在脂肪生成中受到正向调节。在本研究中,在人前脂肪细胞分化诱导后的第15天,用TNF-α、IL-6、瘦素或抵抗素处理成熟的人脂肪细胞。我们证明,TNF-α、IL-6和瘦素上调了miR-378的表达,表明miR-378可能是与肥胖相关的胰岛素抵抗发展中的一种新型介质。