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O-糖基化修饰调节高血糖诱导的 GPX1 激活。

O-GlcNAcylation regulates hyperglycemia-induced GPX1 activation.

机构信息

Department of Biology, Yonsei University, Seoul 120-749, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2010 Jan 1;391(1):756-61. doi: 10.1016/j.bbrc.2009.11.133. Epub 2009 Nov 26.

Abstract

Hyperglycemia induces activation of glutathione peroxidase 1 (GPX1), an anti-oxidant enzyme essential for cell survival during oxidative stress. However, the mechanism of GPX1 activation is unclear. Here, we report that hyperglycemia-induced protein glycosylation by O-linked N-acetylglucosamine (O-GlcNAc) is crucial for activation of GPX1 and for its binding to c-Abl and Arg kinases. GPX1 itself is modified with O-GlcNAc on its C-terminus. We also demonstrate that pharmacological injection of the O-GlcNAcase inhibitor NTZ induces GPX1 activation in the mouse liver. Our findings suggest a crucial role for GPX1 and its O-GlcNAc modification in hyperglycemia and diabetes mellitus.

摘要

高血糖诱导谷胱甘肽过氧化物酶 1(GPX1)的激活,GPX1 是一种抗氧化酶,在氧化应激期间对细胞存活至关重要。然而,GPX1 的激活机制尚不清楚。在这里,我们报告高血糖诱导的 O-连接 N-乙酰葡萄糖胺(O-GlcNAc)对蛋白质的糖基化对于 GPX1 的激活及其与 c-Abl 和 Arg 激酶的结合至关重要。GPX1 自身在其 C 末端被 O-GlcNAc 修饰。我们还证明了 O-GlcNAcase 抑制剂 NTZ 的药理注射可诱导小鼠肝脏中 GPX1 的激活。我们的研究结果表明 GPX1 及其 O-GlcNAc 修饰在高血糖和糖尿病中起关键作用。

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