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星形胶质细胞谷氨酸转运体GLT1的缺失改变了SOD1(G93A)小鼠的疾病状况。

Loss of the astrocyte glutamate transporter GLT1 modifies disease in SOD1(G93A) mice.

作者信息

Pardo Andrea C, Wong Victor, Benson Leah M, Dykes Margaret, Tanaka Kohichi, Rothstein Jeffrey D, Maragakis Nicholas J

机构信息

Department of Neurology, Johns Hopkins University, 600 N. Wolfe St., Meyer 6-119, Baltimore, MD 21287, USA.

出版信息

Exp Neurol. 2006 Sep;201(1):120-30. doi: 10.1016/j.expneurol.2006.03.028. Epub 2006 Jun 6.

Abstract

Recent studies have highlighted the role of astrocytes in the development of motor neuron disease in animal models. The astrocyte glutamate transporter GLT1 is responsible for a significant portion of glutamate transport from the synaptic cleft; regulating synaptic transmission and preventing glutamate excitotoxicity. While previous studies have demonstrated reductions in GLT1 with SOD1-mediated disease progression, it is not well established whether a reduction in this astrocyte-specific transporter alters the pathobiology of motor neuron degeneration in the SOD1(G93A) mouse. In order to address this possible astrocyte-specific influence, we crossed the SOD1(G93A) mouse line with a mouse heterozygous for GLT1 (GLT1+/-) exhibiting a significant reduction in transporter protein. Mice that carried both the SOD1 mutation and a reduced amount of GLT1 (SOD1(G93A)/GLT1+/-) exhibited an increase in the rate of motor decline accompanied by earlier motor neuron loss when compared with SOD1(G93A) mice. A modest reduction in survival was also noted in these mice. Dramatic losses of the GLT1 protein and reduced glutamate transport in the lumbar spinal cords of the SOD1(G93A)/GLT1+/- animals were also observed. GLT1 was not significantly changed in cortices from these animals suggesting that the effect of mutant SOD1 on GLT1 production/function was largely targeted to spinal cord rather than cortical astrocytes. This study suggests that astrocytes, and the astrocyte glutamate transporter GLT1, play a role in modifying disease progression and motor neuron loss in this model.

摘要

最近的研究突出了星形胶质细胞在动物模型运动神经元疾病发展中的作用。星形胶质细胞谷氨酸转运体GLT1负责从突触间隙转运相当一部分谷氨酸;调节突触传递并防止谷氨酸兴奋性毒性。虽然先前的研究已证明随着SOD1介导的疾病进展GLT1会减少,但这种星形胶质细胞特异性转运体的减少是否会改变SOD1(G93A)小鼠运动神经元变性的病理生物学尚不清楚。为了解决这种可能的星形胶质细胞特异性影响,我们将SOD1(G93A)小鼠品系与GLT1杂合小鼠(GLT1+/-)杂交,该小鼠的转运体蛋白显著减少。与SOD1(G93A)小鼠相比,同时携带SOD1突变和减少量GLT1的小鼠(SOD1(G93A)/GLT1+/-)运动功能衰退速率增加,伴有更早的运动神经元丧失。这些小鼠的生存期也有适度缩短。在SOD1(G93A)/GLT1+/-动物的腰脊髓中还观察到GLT1蛋白显著缺失和谷氨酸转运减少。这些动物皮质中的GLT1没有明显变化,这表明突变型SOD1对GLT1产生/功能的影响主要针对脊髓星形胶质细胞而非皮质星形胶质细胞。这项研究表明,星形胶质细胞以及星形胶质细胞谷氨酸转运体GLT1在该模型中对疾病进展和运动神经元丧失具有调节作用。

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