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突触结合蛋白-1在星形胶质细胞生成中起关键作用:对唐氏综合征可能具有的相关性。

Synaptojanin-1 plays a key role in astrogliogenesis: possible relevance for Down's syndrome.

作者信息

Herrera F, Chen Q, Fischer W H, Maher P, Schubert D R

机构信息

Cellular Neurobiology Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037-1099, USA.

出版信息

Cell Death Differ. 2009 Jun;16(6):910-20. doi: 10.1038/cdd.2009.24. Epub 2009 Mar 13.

Abstract

There is increasing interest in gliogenesis as the relevance of glia to both brain development and pathology becomes better understood. However, little is known about this process. The use of multidimensional protein identification technology (MudPIT) to identify changes in phosphoprotein levels in rat neural precursor cells treated with cytokines or retinoic acid showed that phosphorylation of the catalytic subunit of phosphatidylinositol-4,5-bisphosphate 3-kinase (PI3K p110alpha) and dephosphorylation of the inositol phosphatase synaptojanin-1 were common to the gliogenic stimuli. Although PI3K was found to be involved in both neuro- and astrogliogenesis, synaptojanin-1 was specifically involved in astrogliogenesis of neural precursor cells. The role of synaptojanin-1 in astrogliogenesis was further confirmed by analysis of neuron- and glia-specific markers in synaptojanin-1 knockout mouse brain. Additional experiments showed that the Sac1-like phosphatase domain of synaptojanin-1 is responsible for the observed astrogliogenic effect. Our results strongly indicate that phosphatidylinositol metabolism plays a key role in astrogliogenesis. The relevance of our findings for Down's syndrome pathology is discussed.

摘要

随着神经胶质细胞在脑发育和病理学中的相关性得到更好的理解,人们对神经胶质生成的兴趣与日俱增。然而,关于这个过程我们知之甚少。使用多维蛋白质鉴定技术(MudPIT)来鉴定用细胞因子或视黄酸处理的大鼠神经前体细胞中磷酸化蛋白水平的变化,结果显示磷脂酰肌醇-4,5-二磷酸3-激酶(PI3K p110α)催化亚基的磷酸化以及肌醇磷酸酶突触结合蛋白-1的去磷酸化是神经胶质生成刺激的共同特征。虽然发现PI3K参与神经发生和星形胶质细胞生成,但突触结合蛋白-1特别参与神经前体细胞的星形胶质细胞生成。通过分析突触结合蛋白-1基因敲除小鼠脑中的神经元和神经胶质细胞特异性标志物,进一步证实了突触结合蛋白-1在星形胶质细胞生成中的作用。额外的实验表明,突触结合蛋白-1的类Sac1磷酸酶结构域对观察到的星形胶质细胞生成效应负责。我们的结果强烈表明磷脂酰肌醇代谢在星形胶质细胞生成中起关键作用。本文还讨论了我们的发现与唐氏综合征病理学的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdcc/2807404/9d27217f50aa/nihms117700f1.jpg

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