PI3K/AKT/PTEN通路在非酒精性脂肪肝细胞信号传导中的作用

ISRN endocrinology Pub Date : 2013-01-01 Epub Date: 2013-01-30 DOI:10.1155/2013/472432
Satoru Matsuda, Mayumi Kobayashi, Yasuko Kitagishi
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引用次数: 125

摘要

非酒精性脂肪性肝病(NAFLD)是最常见的肝脏病理形式,与肥胖和代谢综合征有关,代谢综合征是一系列与2型糖尿病风险增加相关的脂肪性肝病。如何从单纯性脂肪肝转变为非酒精性脂肪性肝炎(NASH)的分子机制尚不清楚。然而,越来越多的证据表明,肝细胞中磷脂酰肌醇3-激酶(PI3K)/AKT通路的失调是与代谢功能障碍(包括肥胖、代谢综合征和NAFLD)相关的常见分子事件。肿瘤抑制因子PTEN通过其脂质磷酸酶活性负调控PI3K/AKT通路。NAFLD的分子研究支持PTEN在肝脏胰岛素敏感性和脂肪变性、脂肪性肝炎和纤维化的发展中的关键作用。我们回顾了PTEN和PI3K/AKT通路的最新研究,并讨论了NAFLD信号通路中涉及的蛋白质功能。导致这些疾病的分子机制是大量研究的主题,因为更好地了解其发病机制将导致新的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Roles for PI3K/AKT/PTEN Pathway in Cell Signaling of Nonalcoholic Fatty Liver Disease.

Nonalcoholic fatty liver disease (NAFLD) is the most common form of liver pathologies and is associated with obesity and the metabolic syndrome, which represents a range of fatty liver diseases associated with an increased risk of type 2 diabetes. Molecular mechanisms underlying how to make transition from simple fatty liver to nonalcoholic steatohepatitis (NASH) are not well understood. However, accumulating evidence indicates that deregulation of the phosphatidylinositol 3-kinase (PI3K)/AKT pathway in hepatocytes is a common molecular event associated with metabolic dysfunctions including obesity, metabolic syndrome, and the NAFLD. A tumor suppressor PTEN negatively regulates the PI3K/AKT pathways through its lipid phosphatase activity. Molecular studies in the NAFLD support a key role for PTEN in hepatic insulin sensitivity and the development of steatosis, steatohepatitis, and fibrosis. We review recent studies on the features of the PTEN and the PI3K/AKT pathway and discuss the protein functions in the signaling pathways involved in the NAFLD. The molecular mechanisms contributing to the diseases are the subject of considerable investigation, as a better understanding of the pathogenesis will lead to novel therapies for a condition.

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