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封面文章:谷氨酸转运体GLAST和GLT1对大脑发育的不可或缺性。

From the Cover: Indispensability of the glutamate transporters GLAST and GLT1 to brain development.

作者信息

Matsugami Toshiko R, Tanemura Kentaro, Mieda Michihiro, Nakatomi Reiko, Yamada Keiko, Kondo Takashi, Ogawa Masaharu, Obata Kunihiko, Watanabe Masahiko, Hashikawa Tsutomu, Tanaka Kohichi

机构信息

Laboratory of Molecular Neuroscience, School of Biomedical Science and Medical Research Institute, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo 113-8510, Japan.

出版信息

Proc Natl Acad Sci U S A. 2006 Aug 8;103(32):12161-6. doi: 10.1073/pnas.0509144103. Epub 2006 Jul 31.

Abstract

Previous in vitro studies have shown that the neurotransmitter glutamate is important in brain development. Paradoxically, loss-of-function mouse models of glutamatergic signaling that are generated by genetic deletion of glutamate receptors or glutamate release show normal brain assembly. We examined the direct consequences on brain development of extracellular glutamate buildup due to the depletion of the glutamate transporters GLAST and GLT1. GLAST/GLT1 double knockout mice show multiple brain defects, including cortical, hippocampal, and olfactory bulb disorganization with perinatal mortality. Here, we report abnormal formation of the neocortex in GLAST/GLT1 mutants. Several essential aspects of neuronal development, such as stem cell proliferation, radial migration, neuronal differentiation, and survival of SP neurons, were impaired. These results provide direct in vivo evidence that GLAST and GLT1 are necessary for brain development through regulation of extracellular glutamate concentration and show that an important mechanism is likely to be maintenance of glutamate-mediated synaptic transmission.

摘要

先前的体外研究表明,神经递质谷氨酸在大脑发育中很重要。矛盾的是,通过谷氨酸受体基因缺失或谷氨酸释放产生的谷氨酸能信号功能丧失小鼠模型显示大脑组装正常。我们研究了由于谷氨酸转运体GLAST和GLT1耗竭导致细胞外谷氨酸积累对大脑发育的直接影响。GLAST/GLT1双敲除小鼠表现出多种脑缺陷,包括皮质、海马和嗅球结构紊乱以及围产期死亡。在此,我们报告了GLAST/GLT1突变体中新皮质的异常形成。神经元发育的几个重要方面,如干细胞增殖、放射状迁移、神经元分化和SP神经元的存活,均受到损害。这些结果提供了直接的体内证据,表明GLAST和GLT1通过调节细胞外谷氨酸浓度对大脑发育是必需的,并表明一个重要机制可能是维持谷氨酸介导的突触传递。

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