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瘦素在体内和体外均可增加成年海马体神经发生。

Leptin increases adult hippocampal neurogenesis in vivo and in vitro.

作者信息

Garza Jacob C, Guo Ming, Zhang Wei, Lu Xin-Yun

机构信息

Department of Pharmacology, University of Texas Health Science Center, San Antonio, TX 78229, USA.

出版信息

J Biol Chem. 2008 Jun 27;283(26):18238-47. doi: 10.1074/jbc.M800053200. Epub 2008 Mar 26.

Abstract

Leptin, an adipose-derived hormone, has been implicated in several physiological processes involving the hippocampus. However, the role of leptin in adult hippocampal neurogenesis remains unknown. Here we show that leptin regulates neurogenesis in the dentate gyrus of adult mice as well as in cultured adult hippocampal progenitor cells. Chronic administration of leptin to adult mice increased cell proliferation without significant effects on the differentiation and the survival of newly proliferated cells in the dentate gyrus. The expression of the long form leptin receptor, LepRb, was detected in hippocampal progenitor cells by reverse transcription-PCR and immunohistochemistry. Leptin treatment also increased proliferation of cultured adult hippocampal progenitor cells. Analysis of signal transduction pathways revealed that leptin stimulated phosphorylation of Akt and STAT3 but not ERK1/2. Furthermore, pre-treating the cells with specific inhibitors of Akt or STAT3 attenuated leptin-induced cell proliferation in a dose-dependent manner. Taken together, our results support a role for leptin in adult hippocampal neurogenesis and suggest the involvement of the Akt and STAT3 signaling pathways in mediating the actions of leptin on neurogenesis.

摘要

瘦素是一种由脂肪组织分泌的激素,它参与了多个涉及海马体的生理过程。然而,瘦素在成体海马神经发生中的作用尚不清楚。在此,我们表明瘦素可调节成年小鼠齿状回以及培养的成年海马祖细胞中的神经发生。对成年小鼠长期施用瘦素可增加细胞增殖,但对齿状回中新增殖细胞的分化和存活没有显著影响。通过逆转录 - PCR和免疫组织化学在海马祖细胞中检测到了长型瘦素受体LepRb的表达。瘦素处理也增加了培养的成年海马祖细胞的增殖。信号转导通路分析显示,瘦素刺激了Akt和STAT3的磷酸化,但未刺激ERK1/2。此外,用Akt或STAT3的特异性抑制剂预处理细胞以剂量依赖的方式减弱了瘦素诱导的细胞增殖。综上所述,我们的结果支持瘦素在成体海马神经发生中的作用,并表明Akt和STAT3信号通路参与介导瘦素对神经发生的作用。

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