首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Ectopic positioning of Bergmann glia and impaired cerebellar wiring in Mlc1‐over‐expressing mice
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Ectopic positioning of Bergmann glia and impaired cerebellar wiring in Mlc1‐over‐expressing mice

机译:Bergmann Glia的异位定位和MLC1过度表达小鼠中的小脑布线受损

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摘要

Abstract Mlc1 is a causative gene for megalencephalic leukoencephalopathy with subcortical cysts, and is expressed in astrocytes. Mlc1‐over‐expressing mice represent an animal model of early‐onset leukoencephalopathy, which manifests as astrocytic swelling followed by myelin membrane splitting in the white matter. It has been previously reported that Mlc1 is highly expressed in Bergmann glia, while the cerebellar phenotypes of Mlc1‐over‐expressing mouse have not been characterized. Here, we examined the cerebellum of Mlc1‐over‐expressing mouse and found that the distribution of Bergmann glia ( BG ) was normally compacted along the Purkinje cell ( PC ) layer until postnatal day 10 (P10), while most BG were dispersed throughout the molecular layer by P28. Ectopic BG were poorly wrapped around somatodendritic elements of PC s and exhibited reduced expression of the glutamate transporter glutamate‐aspartate transporter. Extraordinarily slow and small climbing fiber ( CF )‐mediated excitatory post‐synaptic currents, which are known to be elicited under accelerated glutamate spillover, emerged at P20‐P28 when BG ectopia was severe, but not at P9‐P12 when ectopia was mild. Furthermore, maturation of CF wiring, which translocates the site of innervation from somata to proximal dendrites, was also impaired. Manipulations that restricted the Mlc1‐over‐expressing period successfully generated mice with and without BG ectopia, depending on the over‐expressing period. Together, these findings suggest that there is a critical time window for mechanisms that promote the positioning of BG in the PC layer. Once normal positioning of BG is affected, the differentiation of BG is impaired, leading to insufficient glial wrapping, exacerbated glutamate spillover, and aberrant synaptic wiring in PC s. Open Practices Open Science: This manuscript was awarded with the Open Materials Badge. For more information see: https://cos.io/our-services/open-science-badges/ Cover Image for this issue: doi: 10.1111/jnc.14199 .
机译:摘要MLC1是具有皮下囊肿的Mugalularic白细胞病变的致病基因,并以星形胶质细胞表达。 MLC1过度表达的小鼠代表早期发作白细胞病变的动物模型,其表现为星形胶质肿胀,然后是白质膜分裂。之前报道,MLC1在Bergmann Glia中高度表达,而MLC1过度表达小鼠的小脑表型尚未表现出来。在这里,我们检查了MLC1过度表达的小鼠的小脑,发现Bergmann Glia(BG)的分布通常沿着Purkinje细胞(PC)层压实直至产后第10天(P10),而大多数BG分散在整个中分子层P28。异位Bg缠绕在PC S的Sematodendritic元素周围,并表现出谷氨酸转运蛋白谷氨酸 - 天冬氨酸转运蛋白转运蛋白转运蛋白转运蛋白的表达。在P20-P28的加速谷氨酸溢出率下,众所周知的兴奋性后突出电流非常缓慢,较小的攀爬纤维(CF)介绍的兴奋性后突出性电流在P20-P28时出现,但当BG异位差异严重时,但在侧普亚岛温和时不在P9-P12处。此外,CF布线的成熟,也损害了从躯体向近端树突中转向躯体的支配部位。限制MLC1过度表达时期的操纵成功地生成了具有和不含BG异位的小鼠,这取决于过表达时期。这些研究结果表明,对于促进BG在PC层中的定位的机制,存在关键的时间窗口。一旦BG的正常定位受到影响,BG的分化会受到损害,导致胶质包装不足,加剧谷氨酸溢出,以及PC S中的异常突触布线。开放实践公开科学:此手稿是授予开放材料徽章的奖励。有关更多信息,请参阅:https://cos.io/our-services/open-cience-badges/封面图片此问题:DOI:10.1111 / JNC.14199。

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