大鼠大脑和小脑皮质肌聚糖染色模式变异性的免疫荧光研究

G. Rizzo, D. Mauro, G. Cutroneo, P. Schembri-Wismayer, Dario Brunetto, Cecilia Spoto, G. Vermiglio, A. Centofanti, A. Favaloro
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引用次数: 0

摘要

题目:大鼠大脑和小脑皮层肌聚糖染色模式变异的免疫荧光研究。背景:肌聚糖是连接细胞外基质成分和细胞骨架的跨膜糖蛋白。这种蛋白质系统在肌肉中的研究已经进行了很长时间,但关于其在非肌肉组织中的定位的数据很少。方法和发现:在本报告中,我们对正常大鼠的大脑和小脑皮层进行了间接免疫荧光研究。结果表明,在这些区域中,每个肌聚糖都以“斑点样”的染色模式表达,斑点的平均直径为0.5-2 μm,主要延伸到神经元和神经胶质细胞的体细胞周围。在大脑皮层中,尽管所有的肌聚糖都存在,但在不同的大脑皮层区域,每种肌聚糖的染色模式存在差异。相反,肌聚糖在小脑皮层的模式分布水平没有改变。我们还进行了统计分析,证实了免疫荧光结果。结论:因此,已知存在多个突触网络的大脑皮层中存在肌聚糖变异性,而小脑皮层中不存在肌聚糖变异性,在小脑皮层中相同的突触网络不变地重复,这表明在大脑中肌聚糖可能与突触网络有关。此外,肌聚糖的分布,主要在神经元的突触后区域,表明这些蛋白在细胞信号传导中起作用,调节膜受体的组装。我们也支持神经胶质细胞中的肌聚糖可能与脑血屏障的调节机制有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Immunofluorescence Study About Staining Pattern Variability of Sarcoglycans in Ratâs Cerebral and Cerebellar Cortex
Title: An Immunofluorescence Study About Staining Pattern Variability of Sarcoglycans in Rat’s Cerebral and Cerebellar Cortex. Background: Sarcoglycans are transmembrane glycoproteins which connect extracellular matrix components to cytoskeleton. This protein system has been long studied in muscle but there are few data about its localization in non-muscular tissues. Methods and Findings: In the present report, we have conducted an indirect immunofluorescence study on normal rat’s cerebral and cerebellar cortex. Our results show that in these districts each sarcoglycan is expressed by a “spot-like” staining pattern, with spots of 0.5-2 μm average diameter, extending mainly around the soma of neurons and glial cells. In cerebral cortex, although all sarcoglycans are present, a staining pattern variability for each sarcoglycan, in the different cerebral cortex areas, exists. Instead, the pattern distribution level of sarcoglycans in cerebellar cortex doesn’t change. We also performed a statistical analysis which confirms the immunofluorescence results. Conclusions: Then, the presence of a sarcoglycans variability in cerebral cortex, where it is known the existence of several synaptic network, and the absence of a sarcoglycans variability in cerebellar cortex, where the same synaptic networks are repeated unchanged, suggest that in brain sarcoglycans may be associated with synaptic networks. Moreover, the distribution of sarcoglycans, mainly in post-synaptic regions of the neurons, suggests a role of these proteins in cellular signalling, regulating membrane receptors assembly. We also support that sarcoglycans in glial cells could be associated with the regulation of the mechanism in the brain-blood-barrier.
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