腹侧手术入路下橄榄损伤。病变部位和小脑的星形细胞反应的时空特征。

K Ito, Y Ishikawa, R D Skinner, R E Mrak, M Morrison-Bogorad, J Mukawa, W S Griffin
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引用次数: 10

摘要

激活的星形胶质细胞是中枢神经系统局部和远端(轴突靶区)损伤反应的内在成分,现在被认为是许多神经系统疾病的活性代谢和调节介质。为了进一步确定这些反应,我们设计了一种新的腹侧手术入路来单侧损伤下橄榄核复合体,该复合体有一个主要的远程靶点,小脑。激活的星形胶质细胞数量、体积、密度以及参与星形胶质细胞反应的脑干总体积均在病变后第4天达到峰值,在第24天向未手术对照值靠拢,但未向未手术对照值靠拢(p < 0.05)。相反,小脑星形胶质细胞反应的峰值延迟,在pld 6时达到最大(与对照组或pld 2相比,p < 0.05)。这些反应与S100 β(一种星形胶质细胞衍生的神经突生长因子)过表达的增加以及小脑稳态神经元损伤反应蛋白β -淀粉样前体蛋白(β - app)水平的增加有关。这与癫痫和阿尔茨海默病中发现的这两种蛋白质的相关增加相似。我们的研究定义了远端星形细胞和神经元反应,这对于理解阿尔茨海默病等疾病中神经病理变化扩散背后的神经胶质-神经元机制可能很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lesioning of the inferior olive using a ventral surgical approach. Characterization of temporal and spatial astrocytic responses at the lesion site and in cerebellum.

Activated astrocytes, intrinsic components of both local and remote (axonal target regions) central nervous system injury responses, are now recognized as active metabolic and regulatory mediators in many neurological disorders. To further define these responses, we devised a new ventral surgical approach to unilaterally lesion the inferior olivary nuclear complex, which has a single predominant remote target, the cerebellum. Activated astrocyte number, volume, and density, as well as the total volume of brainstem involved in the astrocytic response, all peaked at postlesion day (pld) 4, returning toward, but not to, unoperated control values at pld 24 (p < 0.05). In contrast, the peak astrocyte response in the cerebellum was delayed, being greatest at pld 6 (p < 0.05 compared to control or pld 2). These responses were associated with increases in overexpression of S100 beta, an astrocyte-derived neurite growth factor, and with an increase in cerebellar steady-state levels of a neuronal injury response protein, the beta-amyloid precursor protein (beta-APP). This is similar to correlated increases in these two proteins that are found in epilepsy and Alzheimer disease. Our studies defining remote astrocytic and neuronal responses may be important for understanding glial-neuronal mechanisms underlying the spread of neuropathological changes in conditions such as Alzheimer disease.

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