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白血病抑制因子通过Akt磷酸化和14-3-3的上调在少突胶质细胞中诱导抗凋亡反应。

Leukemia inhibitory factor induces an antiapoptotic response in oligodendrocytes through Akt-phosphorylation and up-regulation of 14-3-3.

作者信息

Slaets Helena, Dumont Debora, Vanderlocht Joris, Noben Jean-Paul, Leprince Pierre, Robben Johan, Hendriks Jerome, Stinissen Piet, Hellings Niels

机构信息

Hasselt University, Biomedical Research Institute and Transnationale Universiteit Limburg, School of Life Sciences, Diepenbeek, Belgium.

出版信息

Proteomics. 2008 Mar;8(6):1237-47. doi: 10.1002/pmic.200700641.

Abstract

Leukemia inhibitory factor (LIF) promotes the survival of oligodendrocytes (OLG) both in vitro and in an animal model of multiple sclerosis. Here, we show that LIF protects mature rat OLG cultures selectively against the combined insult of the proinflammatory cytokines interferon-gamma and tumor necrosis factor-alpha, but it does not protect against oxidative stress nor against staurosporine induced apoptosis. We further demonstrate that LIF activates the janus kinase (JAK)/signal transducer and activator of transcription 3 (STAT3) and the phosphatidylinositol 3 kinase/Akt pathway in mature OLG. We show that LIF protection is independent of suppressors of cytokine signaling and Bcl-2 mRNA expression levels. To gain further insight into the protective mechanism, a quantitative proteomic approach (DIGE) was applied to identify differentially expressed proteins in LIF-treated OLG. Our results indicate that LIF induces a shift in the cellular machinery toward a prosurvival execution program, illustrated by an enhanced expression of isoforms of the antiapoptotic molecule 14-3-3. These data provide further insight into the mechanisms of LIF-mediated protection of mature OLGs.

摘要

白血病抑制因子(LIF)在体外和多发性硬化症动物模型中均能促进少突胶质细胞(OLG)的存活。在此,我们表明LIF可选择性地保护成熟大鼠OLG培养物免受促炎细胞因子γ干扰素和肿瘤坏死因子-α的联合损伤,但它不能保护细胞免受氧化应激或星形孢菌素诱导的细胞凋亡。我们进一步证明,LIF可激活成熟OLG中的janus激酶(JAK)/信号转导子和转录激活子3(STAT3)以及磷脂酰肌醇3激酶/Akt信号通路。我们表明,LIF的保护作用独立于细胞因子信号转导抑制因子和Bcl-2 mRNA表达水平。为了进一步深入了解其保护机制,我们应用了定量蛋白质组学方法(差异凝胶电泳,DIGE)来鉴定LIF处理的OLG中差异表达的蛋白质。我们的结果表明,LIF诱导细胞机制向促生存执行程序转变,这表现为抗凋亡分子14-3-3的异构体表达增强。这些数据为LIF介导的成熟OLG保护机制提供了进一步的见解。

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