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神经节苷脂特异性唾液酸酶NEU3在肝脏中的表达增加可改善小鼠的胰岛素敏感性和糖耐量。

Increased hepatic expression of ganglioside-specific sialidase, NEU3, improves insulin sensitivity and glucose tolerance in mice.

作者信息

Yoshizumi Shinsuke, Suzuki Susumu, Hirai Masashi, Hinokio Yoshinori, Yamada Tetsuya, Yamada Takahiro, Tsunoda Uiko, Aburatani Hiroyuki, Yamaguchi Kazunori, Miyagi Taeko, Oka Yoshitomo

机构信息

Department of Metabolism and Diabetes, Tohoku University School of Medicine, Sendai 980-8574, Japan.

出版信息

Metabolism. 2007 Mar;56(3):420-9. doi: 10.1016/j.metabol.2006.10.027.

Abstract

Membrane microdomains rich in gangliosides are recognized as being critical for proper compartmentalization of insulin signaling. Plasma membrane-associated sialidase, NEU3, is a key enzyme for ganglioside hydrolysis. We previously reported that mice overexpressing NEU3 mainly in muscles developed severe insulin-resistant diabetes. To examine the possible contributions of NEU3 to in vivo insulin sensitivity and glucose tolerance, NEU3 was expressed by using adenoviral vectors in the livers of C57BL/6 mice on standard and high-fat diets, and insulin-resistant KKAy mice on standard diets. Hepatic NEU3 overexpression paradoxically improved glucose tolerance and insulin sensitivity in the C57BL/6 mice fed standard diets, and glucose tolerance in the C57BL/6 mice fed high-fat diets and in KKAy mice. Hepatic NEU3 overexpression increased hepatic glycogen deposition and triglyceride accumulation, and enhanced the hepatic peroxisome proliferator-activated receptor gamma and fetuin expression in the C57BL/6 mice on standard and high-fat diets, and in KKAy mice. Thin-layer chromatographic analysis demonstrated increased levels of GM1 and markedly reduced GM3 in the livers of mice with hepatic NEU3 overexpression (NEU3 mice). Basal and insulin-stimulated tyrosine phosphorylations of insulin receptor substrate 1 were significantly increased, but tyrosine phosphorylations of the insulin receptor and insulin receptor substrate 2 in the NEU3 liver were unchanged. Insulin-stimulated tyrosine phosphorylations of the insulin receptor were increased in adipose tissues of NEU3 mice. These results suggest that hepatic NEU3 overexpression improves insulin sensitivity and glucose tolerance through modification of ganglioside composition and peroxisome proliferator-activated receptor gamma signaling. Our findings also provide further evidence that NEU3 is an important regulator of insulin sensitivity and glucose tolerance.

摘要

富含神经节苷脂的膜微区被认为对胰岛素信号的正确区室化至关重要。与质膜相关的唾液酸酶NEU3是神经节苷脂水解的关键酶。我们之前报道过,主要在肌肉中过表达NEU3的小鼠会发展为严重的胰岛素抵抗性糖尿病。为了研究NEU3对体内胰岛素敏感性和葡萄糖耐量的可能作用,我们使用腺病毒载体在标准饮食和高脂饮食的C57BL/6小鼠肝脏以及标准饮食的胰岛素抵抗KKAy小鼠肝脏中表达NEU3。矛盾的是,肝脏中NEU3的过表达改善了标准饮食喂养的C57BL/6小鼠的葡萄糖耐量和胰岛素敏感性,以及高脂饮食喂养的C57BL/6小鼠和KKAy小鼠的葡萄糖耐量。肝脏中NEU3的过表达增加了肝脏糖原沉积和甘油三酯积累,并增强了标准饮食和高脂饮食的C57BL/6小鼠以及KKAy小鼠肝脏中过氧化物酶体增殖物激活受体γ和胎球蛋白的表达。薄层色谱分析表明,肝脏NEU3过表达的小鼠(NEU3小鼠)肝脏中GM1水平升高,GM3水平显著降低。胰岛素受体底物1的基础酪氨酸磷酸化和胰岛素刺激的酪氨酸磷酸化显著增加,但NEU3肝脏中胰岛素受体和胰岛素受体底物2的酪氨酸磷酸化未发生变化。NEU3小鼠脂肪组织中胰岛素刺激的胰岛素受体酪氨酸磷酸化增加。这些结果表明,肝脏中NEU3的过表达通过改变神经节苷脂组成和过氧化物酶体增殖物激活受体γ信号传导来改善胰岛素敏感性和葡萄糖耐量。我们的研究结果还进一步证明NEU3是胰岛素敏感性和葡萄糖耐量的重要调节因子。

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