小脑突触发生:突变小鼠-神经元移植。

Journal de physiologie Pub Date : 1991-01-01
C Sotelo
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引用次数: 0

摘要

影响小鼠小脑的神经突变为研究与突触连接建立有关的一些细胞机制提供了可能性(见Sotelo, 1990)。事实上,这些突变通过明确的病变引起突触形成正常过程的破坏,并且通过检查成人小脑连通性的扰动,有可能解开突触发生过程中发生的许多复杂的细胞相互作用。此外,其中一些突变主要影响浦肯野细胞,浦肯野细胞是小脑皮层的关键成分,也是它唯一的输出物,导致它们退化。这些浦肯野细胞缺陷的小脑提供了一种最佳材料,通过移植实验来尝试取代缺失的神经元,并分析不同生物年龄的神经元伙伴之间的突触发生过程:宿主成年神经元和胚胎移植的浦肯野细胞(Sotelo et al., 1990)。本文的目的是总结我的实验室在上述两个课题上所做的一些工作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cerebellar synaptogenesis: mutant mice--neuronal grafting.

Neurological mutations affecting the cerebellum of the mouse have offered the possibility to study some of the cellular mechanisms involved in the establishment of synaptic connections (see in Sotelo, 1990). Indeed, these mutations provoke through well-defined lesions, the disruption of the normal processes of synapse formation and, by examination of the perturbations in the adult cerebellar connectivity, it is possible to unravel some of the numerous and intricate cellular interactions taking place during synaptogenesis. Furthermore, some of these mutants primarily affect Purkinje cells, the pivotal elements of the cerebellar cortex and its only output, inducing their degeneration. These Purkinje cell-deficient cerebella offer an optimal material to try--by grafting experiments--to replace the missing neurons, and to analyze synaptogenic processes between neuronal partners of different biological ages: the host adult neurons and the embryonary grafted Purkinje cells (Sotelo et al., 1990). The aim of this paper is to summarize some of the work carried out in my laboratory concerning the two above-mentioned topics.

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