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转铁蛋白内化后的少突胶质细胞分化和信号转导:作用机制。

Oligodendrocyte differentiation and signaling after transferrin internalization: a mechanism of action.

机构信息

Cátedra de Química Biológica Patológica, Departamento de Química Biológica, Facultad de Farmacia y Bioquímica (FFyB), Universidad de Buenos Aires (UBA), Instituto de Química y Fisicoquímica Biológica "Prof. Alejandro C. Paladini" (IQUIFIB), UBA-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Junin 965, CABA, Buenos Aires, Argentina.

出版信息

Exp Neurol. 2013 Oct;248:262-74. doi: 10.1016/j.expneurol.2013.06.014. Epub 2013 Jun 21.

DOI:10.1016/j.expneurol.2013.06.014
PMID:23797152
Abstract

Oligodendrocytes are the cells producing the myelin membrane around the axons in the central nervous system and, although apotransferrin (aTf) is required for oligodendrocyte differentiation, the underlying mechanisms are not fully understood. Fyn tyrosine kinase, a member of the Src family of proteins, has been shown to play an important role in myelination by up-regulating the expression of myelin basic protein; however, a molecular link between aTf and Fyn kinase signaling pathway during oligodendrocytes differentiation has not been established yet. Our aim was to investigate whether Fyn kinase, MEK/ERK and PI3K/Akt signaling pathways are required for aTf-stimulation of oligodendrocyte differentiation and also to determine if the transferrin receptor is involved in these mechanisms. Treatment of primary cultures of oligodendroglial precursor cells with aTf leads to Fyn kinase activation by a mechanism that involves transferrin receptor. In turn, Fyn kinase activation promotes MEK-mediated transient phosphorylation of ERK1/2. On the other hand, transferrin receptor internalization also produces rapid and sustained activation of Akt, which involves phosphatidylinositol 3-kinase (PI3K) activation. Finally, aTf incorporated through clathrin-mediated endocytosis increases myelin basic protein, F3-contactin and β-tubulin through Fyn/MEK/ERK pathways, as well as an activation of the PI3K/Akt pathway. Our results also demonstrate that the activation of the pathways necessary for oligodendroglial precursor cell maturation is dependent on AP2 recruitment onto the plasma membrane for clathrin-mediated endocytosis of transferrin receptor.

摘要

少突胶质细胞是在中枢神经系统中产生轴突髓鞘膜的细胞,虽然转铁蛋白(aTf)是少突胶质细胞分化所必需的,但其中的机制尚未完全阐明。Src 家族蛋白中的 Fyn 酪氨酸激酶已被证明通过上调髓鞘碱性蛋白的表达在髓鞘形成中起重要作用;然而,aTf 和 Fyn 激酶信号通路之间的分子联系在少突胶质细胞分化中尚未建立。我们的目的是研究 Fyn 激酶、MEK/ERK 和 PI3K/Akt 信号通路是否是 aTf 刺激少突胶质细胞分化所必需的,以及转铁蛋白受体是否参与这些机制。用 aTf 处理少突胶质前体细胞的原代培养物会导致 Fyn 激酶通过涉及转铁蛋白受体的机制被激活。反过来,Fyn 激酶的激活促进了 MEK 介导的 ERK1/2 的短暂磷酸化。另一方面,转铁蛋白受体的内化也会迅速而持续地激活 Akt,这涉及到磷脂酰肌醇 3-激酶(PI3K)的激活。最后,通过网格蛋白介导的内吞作用摄取的 aTf 通过 Fyn/MEK/ERK 通路增加髓鞘碱性蛋白、F3-结合蛋白和 β-微管蛋白,同时激活 PI3K/Akt 通路。我们的结果还表明,少突胶质前体细胞成熟所必需的途径的激活依赖于 AP2 募集到质膜上,用于网格蛋白介导的转铁蛋白受体的内吞作用。

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