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杂合子 Q140 亨廷顿病小鼠纹状体投射神经元病变之前,皮质纹状体和丘脑纹状体突触末梢丢失。

Loss of corticostriatal and thalamostriatal synaptic terminals precedes striatal projection neuron pathology in heterozygous Q140 Huntington's disease mice.

机构信息

Department of Anatomy and Neurobiology, The University of Tennessee Health Science Center, Memphis, TN 38163, USA.

出版信息

Neurobiol Dis. 2013 Dec;60:89-107. doi: 10.1016/j.nbd.2013.08.009. Epub 2013 Aug 19.

Abstract

Motor slowing, forebrain white matter loss, and striatal shrinkage have been reported in premanifest Huntington's disease (HD) prior to overt striatal neuron loss. We carried out detailed LM and EM studies in a genetically precise HD mimic, heterozygous Q140 HD knock-in mice, to examine the possibility that loss of corticostriatal and thalamostriatal terminals prior to striatal neuron loss underlies these premanifest HD abnormalities. In our studies, we used VGLUT1 and VGLUT2 immunolabeling to detect corticostriatal and thalamostriatal (respectively) terminals in dorsolateral (motor) striatum over the first year of life, prior to striatal projection neuron pathology. VGLUT1+ axospinous corticostriatal terminals represented about 55% of all excitatory terminals in striatum, and VGLUT2+ axospinous thalamostriatal terminals represented about 35%, with VGLUT1+ and VGLUT2+ axodendritic terminals accounting for the remainder. In Q140 mice, a significant 40% shortfall in VGLUT2+ axodendritic thalamostriatal terminals and a 20% shortfall in axospinous thalamostriatal terminals were already observed at 1 month of age, but VGLUT1+ terminals were normal in abundance. The 20% deficiency in VGLUT2+ thalamostriatal axospinous terminals persisted at 4 and 12 months in Q140 mice, and an additional 30% loss of VGLUT1+ corticostriatal terminals was observed at 12 months. The early and persistent deficiency in thalamostriatal axospinous terminals in Q140 mice may reflect a development defect, and the impoverishment of this excitatory drive to striatum may help explain early motor defects in Q140 mice and in premanifest HD. The loss of corticostriatal terminals at 1 year in Q140 mice is consistent with prior evidence from other mouse models of corticostriatal disconnection early during progression, and can explain both the measurable bradykinesia and striatal white matter loss in late premanifest HD.

摘要

运动减慢、前脑白质丢失和纹状体萎缩在明显的纹状体神经元丢失之前已在隐匿性亨廷顿病(HD)中被报道。我们在一种遗传上精确的 HD 模拟物,杂合 Q140 HD 敲入小鼠中进行了详细的 LM 和 EM 研究,以检查在纹状体神经元丢失之前皮质纹状体和丘脑纹状体末端的丢失是否导致这些隐匿性 HD 异常。在我们的研究中,我们使用 VGLUT1 和 VGLUT2 免疫标记物来检测在纹状体投射神经元病理学之前的生命第一年的背外侧(运动)纹状体中的皮质纹状体和丘脑纹状体(分别)末端。VGLUT1+轴突棘皮质纹状体末端代表纹状体中所有兴奋性末端的约 55%,而 VGLUT2+轴突棘丘脑纹状体末端代表约 35%,VGLUT1+和 VGLUT2+轴突树突末端占其余部分。在 Q140 小鼠中,在 1 个月龄时已经观察到 VGLUT2+轴突树突状丘脑纹状体末端的显著 40%短缺和轴突棘状丘脑纹状体末端的 20%短缺,而 VGLUT1+末端的丰度正常。在 Q140 小鼠中,在 4 个月和 12 个月时,VGLUT2+丘脑纹状体轴突棘状末端的 20%缺陷持续存在,并且在 12 个月时观察到 VGLUT1+皮质纹状体末端的额外 30%损失。Q140 小鼠中丘脑纹状体轴突棘状末端的早期和持续缺陷可能反映了发育缺陷,并且这种兴奋性对纹状体的驱动不足可能有助于解释 Q140 小鼠和隐匿性 HD 中的早期运动缺陷。Q140 小鼠中 1 年时皮质纹状体末端的丢失与其他皮质纹状体分离的小鼠模型中早期进展期间的先前证据一致,并且可以解释晚期隐匿性 HD 中的可测量的运动徐缓和纹状体白质丢失。

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Role of cerebral cortex in the neuropathology of Huntington's disease.大脑皮层在亨廷顿病神经病理学中的作用。
Front Neural Circuits. 2013 Feb 18;7:19. doi: 10.3389/fncir.2013.00019. eCollection 2013.

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