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Differential expression of nuclear lamin subtypes in the neural cells of the adult rat cerebral cortex

机译:成年大鼠大脑皮层神经细胞核层粘连蛋白亚型的差异表达

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摘要

Lamins are type V intermediate filament proteins that are located beneath the inner nuclear membrane. In mammalian somatic cells, LMNB1 and LMNB2 encode somatic lamins B1 and B2, respectively, and the LMNA gene is alternatively spliced to generate somatic lamins A and C.Mutations in lamin genes have been linked to many human hereditary diseases, including neurodegenerative disorders. Knowledge about lamins in the nervous system has been accumulated recently, but a precise analysis of lamin subtypes in glial cells has not yet been reported. In this study we investigated the composition of lamin subtypes in neurons, astrocytes, oligodendrocyte-lineage cells, and microglia in the adult rat cerebral cortex using an immunohistochemical staining method. Lamin A was not observed in neurons and glial cells. Lamin C was observed in astrocytes, mature oligodendrocytes and neurons, but not observed in oligodendrocyte progenitor cells. Microglia also did not stain positive for lamin C which differed from macrophages, with lamin C positive. Lamin B1 and B2 were observed in all glial cells and neurons. Lamin B1 was intensely positive in oligodendrocyte progenitor cells compared with other glial cells and neurons. Lamin B2 was weakly positive in all glial cells compared to neurons. Our current study might provide useful information to reveal how the onset mechanisms of human neurodegenerative diseases are associated with mutations in genes for nuclear lamin proteins.
机译:核纤层蛋白是位于内核膜下方的V型中间丝蛋白。在哺乳动物的体细胞中,LMNB1和LMNB2分别编码体层lamin B1和B2,并且将LMNA基因剪接以产生体层lamin A和C.lamin基因的突变与许多人类遗传性疾病有关,包括神经退行性疾病。最近已经积累了有关神经系统中lamin的知识,但尚未报道对神经胶质细胞中lamin亚型的精确分析。在这项研究中,我们使用免疫组织化学染色方法研究了成年大鼠大脑皮层神经元,星形胶质细胞,少突胶质细胞谱系细胞和小胶质细胞中lamin亚型的组成。在神经元和神经胶质细胞中未观察到核纤层蛋白A。在星形胶质细胞,成熟的少突胶质细胞和神经元中观察到层粘连蛋白C,但在少突胶质细胞祖细胞中未观察到。小胶质细胞也没有发现与巨噬细胞不同的lamin C阳性,lamin C阳性。在所有神经胶质细胞和神经元中均观察到了Lamin B1和B2。与其他神经胶质细胞和神经元相比,Lamin B1在少突胶质祖细胞中强烈阳性。与神经元相比,Lamin B2在所有神经胶质细胞中均呈弱阳性。我们当前的研究可能会提供有用的信息,以揭示人类神经退行性疾病的发病机制与核纤层蛋白基因突变有关。

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