Watase K, Hashimoto K, Kano M, Yamada K, Watanabe M, Inoue Y, Okuyama S, Sakagawa T, Ogawa S, Kawashima N, Hori S, Takimoto M, Wada K, Tanaka K
Department of Degenerative Neurological Diseases, National Institute of Neuroscience, Kodaira, Tokyo, Japan.
Eur J Neurosci. 1998 Mar;10(3):976-88. doi: 10.1046/j.1460-9568.1998.00108.x.
To study the function of GLAST, a glutamate transporter highly expressed in the cerebellar Bergmann astrocytes, the mouse GLAST gene was inactivated. GLAST-deficient mice developed normally and could manage simple coordinated tasks, such as staying on a stationary or a slowly rotating rod, but failed more challenging task such as staying on a quickly rotating rod. Electrophysiological examination revealed that Purkinje cells in the mutant mice remained to be multiply innervated by climbing fibres even at the adult stage. We also found that oedema volumes in the mutant mice increased significantly after cerebellar injury. These results indicate that GLAST plays active roles both in the cerebellar climbing fibre synapse formation and in preventing excitotoxic cerebellar damage after acute brain injury.
为了研究谷氨酸转运体GLAST(一种在小脑伯格曼星形胶质细胞中高度表达的谷氨酸转运体)的功能,研究人员使小鼠GLAST基因失活。GLAST基因缺陷的小鼠发育正常,能够完成简单的协调任务,如停留在静止或缓慢旋转的杆上,但在完成更具挑战性的任务(如停留在快速旋转的杆上)时失败。电生理检查显示,即使在成年阶段,突变小鼠的浦肯野细胞仍被攀缘纤维多重支配。我们还发现,突变小鼠在小脑损伤后的水肿体积显著增加。这些结果表明,GLAST在小脑攀缘纤维突触形成以及预防急性脑损伤后兴奋性毒性小脑损伤方面均发挥着积极作用。