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α-突触核蛋白-1转基因小鼠表现出轻度运动障碍。

Synphilin-1 transgenic mice exhibit mild motor impairments.

作者信息

Jin Hong-Guo, Yamashita Hiroshi, Nakamura Takeshi, Fukuba Hiromasa, Takahashi Tetsuya, Hiji Masanori, Kohriyama Tatsuo, Matsumoto Masayasu

机构信息

Department of Clinical Neuroscience and Therapeutics, Hiroshima University Graduate School of Biomedical Sciences, 1-2-3 Kasumi, Hiroshima 734-8551, Japan.

出版信息

Neurosci Lett. 2008 Nov 7;445(1):12-7. doi: 10.1016/j.neulet.2008.08.073. Epub 2008 Aug 31.

Abstract

Synphilin-1 represents a cytoplasmic protein that interacts with alpha-synuclein and localizes close to synaptic vesicles. The interaction of synphilin-1 with several proteins involved in Parkinson's disease suggests that it might be involved in the pathogenesis of the disease. Nonetheless, the function of synphilin-1 remains unclear. In the present study, we generated transgenic mice expressing human synphilin-1 under the prion protein promoter. Synphilin-1 was widely expressed in neurons in the brain including the substantia nigra, where massive loss of dopamine neurons was not observed. In the transgenic mouse brain, synphilin-1 protein was polyubiquitinated, and partially insoluble. Although modified-SHIRPA revealed no significant difference in behavior and morphology, the reduced rotarod performance and step length were observed in transgenic mice as compared with non-transgenic littermates. Synphilin-1 might be involved in motor function, and its accumulation in the central nervous system can cause motor impairments.

摘要

突触核蛋白-1是一种细胞质蛋白,它与α-突触核蛋白相互作用,并定位于靠近突触小泡的位置。突触核蛋白-1与几种帕金森病相关蛋白的相互作用表明,它可能参与了该疾病的发病机制。尽管如此,突触核蛋白-1的功能仍不清楚。在本研究中,我们构建了在朊病毒蛋白启动子控制下表达人突触核蛋白-1的转基因小鼠。突触核蛋白-1在包括黑质在内的大脑神经元中广泛表达,在黑质中未观察到多巴胺能神经元的大量丢失。在转基因小鼠脑中,突触核蛋白-1蛋白发生多聚泛素化,且部分不溶。尽管改良SHIRPA行为学和形态学检测未发现显著差异,但与非转基因同窝小鼠相比,转基因小鼠的转棒试验表现和步长有所降低。突触核蛋白-1可能参与运动功能,其在中枢神经系统中的积累可导致运动障碍。

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