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发育中小鼠大脑中髓磷脂蛋白基因的区域表达:原位杂交研究

Regional expression of myelin protein genes in the developing mouse brain: in situ hybridization studies.

作者信息

Verity A N, Campagnoni A T

机构信息

Mental Retardation Research Center, UCLA School of Medicine 90024.

出版信息

J Neurosci Res. 1988 Oct-Dec;21(2-4):238-48. doi: 10.1002/jnr.490210216.

Abstract

Expression of mRNAs for the two major myelin proteins, myelin basic protein (MBP) and proteolipid protein (PLP), was examined in a number of regions of the developing mouse brain using in situ hybridization. In general, MBP and PLP mRNAs were observed to be coexpressed during ontogeny, prior to the histological appearance of myelin. Expression of both mRNAs was detected as early as 6 hours postpartum in the medulla oblongata and, with development, expression of these mRNAs progressed in a caudal to rostral direction. Peak expression occurred at approximately postnatal day 20 in most regions examined, regardless of time of onset of expression. As myelination proceeded, two different labeling patterns were observed with the PLP and MBP 35S-labeled cDNA probes. In the earliest stages of myelinogenesis MBP mRNA labeling was restricted to oligodendrocyte cell bodies, but shortly after the gene began to be expressed the labeling became more diffuse. In contrast, PLP mRNA labeling remained over or surrounding oligodendrocyte cell bodies at all stages of myelinogenesis. These two distinctly different patterns of labeling are consistent with alternative intracellular trafficking of MBP and PLP mRNAs, in which PLP mRNAs remain associated with ribosomes within the cell soma and MBP mRNAs move from the cell soma to the oligodendrocyte processes at a specific stage early in myelinogenesis. However, there appeared to be a clear time lag between the onset of MBP mRNA expression and the movement of ribosomes carrying MBP mRNAs into the oligodendrocyte processes. Additionally, the in situ hybridization studies revealed a population of unidentified cells residing in cortical molecular layers that express PLP mRNA in the absence of MBP mRNA.

摘要

利用原位杂交技术,在发育中的小鼠大脑的多个区域检测了两种主要髓磷脂蛋白,即髓磷脂碱性蛋白(MBP)和蛋白脂蛋白(PLP)的mRNA表达。一般来说,在髓磷脂组织学出现之前的个体发育过程中,观察到MBP和PLP mRNA是共表达的。早在产后6小时就在延髓中检测到了这两种mRNA的表达,并且随着发育,这些mRNA的表达从尾侧向头侧推进。在大多数检测区域,峰值表达大约出现在出生后第20天,与表达开始的时间无关。随着髓鞘形成的进行,用PLP和MBP 35S标记的cDNA探针观察到两种不同的标记模式。在髓鞘形成的最早阶段,MBP mRNA标记局限于少突胶质细胞胞体,但在基因开始表达后不久,标记变得更加弥散。相反,在髓鞘形成的所有阶段,PLP mRNA标记都保留在少突胶质细胞胞体上或其周围。这两种明显不同的标记模式与MBP和PLP mRNA的细胞内转运方式不同一致,其中PLP mRNA在细胞体中仍与核糖体结合,而MBP mRNA在髓鞘形成早期的特定阶段从细胞体移动到少突胶质细胞突起。然而MBP mRNA表达的开始与携带MBP mRNA的核糖体进入少突胶质细胞突起之间似乎存在明显的时间滞后。此外,原位杂交研究揭示了一群位于皮质分子层的未鉴定细胞,它们在没有MBP mRNA的情况下表达PLP mRNA。

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