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jimpy突变体中的基因表达:少突胶质细胞表达髓鞘蛋白基因减少及髓鞘碱性蛋白mRNA转运受损的证据

Gene expression in the jimpy mutant: evidence for fewer oligodendrocytes expressing myelin protein genes and impaired translocation of myelin basic protein mRNA.

作者信息

Verity A N, Levine M S, Campagnoni A T

机构信息

Mental Retardation Research Center, UCLA School of Medicine.

出版信息

Dev Neurosci. 1990;12(6):359-72. doi: 10.1159/000111864.

Abstract

Myelin basic protein (MBP) and proteolipid protein (PLP) gene expression was investigated in the murine dysmyelinating mutant, jimpy and age-matched normal mice. MBP and PLP mRNA expression was examined in several brain regions by in situ hybridization histochemistry between 10 and 20 days postpartum. The results showed a general reduction in both PLP and MBP mRNA expression throughout in jimpy brain due primarily to fewer numbers of jimpy oligodendrocytes expressing these genes. A less severe, but significant, reduction in the level of PLP expression per oligodendrocyte was also observed in the mutant brain. Because of the diffuse pattern of MBP mRNA distribution in the controls it was not possible to determine whether MBP expression was reduced on a per cell basis in the jimpy mutant. Silver grains representing MBP mRNAs were diffusely distributed over myelinating regions in normal mice but, in contrast, the grains were primarily clustered over oligodendrocyte cell bodies in the jimpy brains. No significant differences in jimpy oligodendrocyte morphology were evident by galactocerebroside immunohistochemistry. These results suggested that the apparent MBP mRNA clustering was not due to truncated or reduced numbers of oligodendrocyte processes. Rather, they suggest that the inability of jimpy mice to incorporate MBP into myelin may be due, in part, to a disruption in the translocation of MBP mRNAs within the oligodendrocyte.

摘要

在小鼠脱髓鞘突变体jimpy和年龄匹配的正常小鼠中研究了髓鞘碱性蛋白(MBP)和蛋白脂蛋白(PLP)基因的表达。在产后10至20天之间,通过原位杂交组织化学检查了几个脑区中MBP和PLP mRNA的表达。结果显示,jimpy脑内PLP和MBP mRNA的表达普遍降低,这主要是由于表达这些基因的jimpy少突胶质细胞数量较少。在突变体脑中还观察到每个少突胶质细胞中PLP表达水平有较轻微但显著的降低。由于对照中MBP mRNA分布呈弥散性,因此无法确定jimpy突变体中MBP表达在单个细胞水平上是否降低。代表MBP mRNA的银颗粒在正常小鼠的髓鞘形成区域弥散分布,但相比之下,这些颗粒主要聚集在jimpy脑内的少突胶质细胞胞体上。通过半乳糖脑苷脂免疫组织化学未发现jimpy少突胶质细胞形态有明显差异。这些结果表明,明显的MBP mRNA聚集并非由于少突胶质细胞突起的截断或数量减少。相反,它们表明jimpy小鼠无法将MBP整合到髓鞘中可能部分是由于少突胶质细胞内MBP mRNA转运的破坏。

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