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人脑肿瘤中神经元核基质蛋白NRP/B的基因组组织、染色体定位及表达调控

Genomic organization, chromosomal localization and regulation of expression of the neuronal nuclear matrix protein NRP/B in human brain tumors.

作者信息

Kim T A, Ota S, Jiang S, Pasztor L M, White R A, Avraham S

机构信息

Division of Experimental Medicine, Beth Israel Deaconess Medical Center, Harvard Institutes of Medicine, 4 Blackfan Circle, 02115, Boston, MA, USA.

出版信息

Gene. 2000 Sep 5;255(1):105-16. doi: 10.1016/s0378-1119(00)00297-3.

Abstract

The nuclear matrix and its role in cell physiology are largely unknown, and the discovery of any matrix constituent whose expression is tissue- and/or cell-specific offers a new avenue of exploration. Studies of the novel neuronal nuclear matrix protein, NRP/B, reveal that it is an early and highly specific marker of neuronal induction and development in vertebrates, since its expression is restricted mainly to the developing and mature nervous system. These studies also show that NRP/B is involved in neuronal differentiation. To further examine the structure-function of NRP/B, we have cloned and characterized the murine Nrp/b gene. The murine gene consists of four exons interrupted by three introns that span 7.6kb of DNA. The complete open reading frame is localized in exon 3, suggesting that NRP/B is highly conserved during evolution. Chromosomal analysis shows that NRP/B is localized to chromosome 13 in mouse and chromosome 5q12-13 in human. Since our previous studies demonstrated that NRP/B is expressed in primary hippocampal neurons but not in primary astrocytes, we have characterized NRP/B mRNA and protein expression in various brain cell lines and in human brain tumors. Abundant expression of NRP/B mRNA and protein was observed in human neuroblastoma cell lines (IMR32, SKN-MC, SKN-SH), in glioblastoma cell lines (A172, T98G, U87-MG, U118-MG, U138-MG, and U373-MG), in neuroglioma (H4) and astrocytoma cell lines (CCF-STTG1 and SW1088). Confocal analysis of NRP/B in U87-MG glioblastoma cells indicated nuclear localization of NRP/B. NRP/B expression was also observed in human primary brain tumors including glioblastoma multiformae and astrocytomas (total of five cases). These results suggest that NRP/B expression is upregulated in human brain tumors including glioblastomas and astrocytomas, while under normal conditions NRP/B expression is restricted to neurons. This study implicates a role for NRP/B in brain tumor development.

摘要

核基质及其在细胞生理学中的作用在很大程度上尚不明确,而发现任何一种其表达具有组织和/或细胞特异性的基质成分都为探索提供了新途径。对新型神经元核基质蛋白NRP/B的研究表明,它是脊椎动物神经元诱导和发育的早期且高度特异性的标志物,因为其表达主要局限于发育中的和成熟的神经系统。这些研究还表明NRP/B参与神经元分化。为了进一步研究NRP/B的结构功能,我们克隆并鉴定了小鼠Nrp/b基因。小鼠基因由四个外显子组成,被三个内含子打断,跨越7.6kb的DNA。完整的开放阅读框位于外显子3中,这表明NRP/B在进化过程中高度保守。染色体分析显示,NRP/B在小鼠中定位于13号染色体,在人类中定位于5q12 - 13染色体。由于我们之前的研究表明NRP/B在原代海马神经元中表达,但在原代星形胶质细胞中不表达,我们已经对各种脑细胞系和人脑肿瘤中NRP/B mRNA和蛋白的表达进行了鉴定。在人神经母细胞瘤细胞系(IMR32、SKN - MC、SKN - SH)、胶质母细胞瘤细胞系(A172、T98G、U87 - MG、U118 - MG、U138 - MG和U373 - MG)、神经胶质瘤(H4)和星形细胞瘤细胞系(CCF - STTG1和SW1088)中观察到NRP/B mRNA和蛋白的大量表达。对U87 - MG胶质母细胞瘤细胞中NRP/B的共聚焦分析表明NRP/B定位于细胞核。在包括多形性胶质母细胞瘤和星形细胞瘤(共5例)在内的人类原发性脑肿瘤中也观察到了NRP/B的表达。这些结果表明,在包括胶质母细胞瘤和星形细胞瘤在内的人脑肿瘤中,NRP/B的表达上调,而在正常情况下,NRP/B的表达局限于神经元。这项研究表明NRP/B在脑肿瘤发展中起作用。

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