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干扰素-γ受体在人神经胶质细胞体内和体外的差异表达。

Differential expression of interferon-gamma receptor on human glial cells in vivo and in vitro.

机构信息

Department of Psychiatry, The University of British Columbia, Vancouver, BC, Canada.

出版信息

J Neuroimmunol. 2010 Aug 25;225(1-2):91-9. doi: 10.1016/j.jneuroim.2010.04.023.

Abstract

Although significant effects of interferon-gamma (IFN-gamma) on glial cells are well documented, information on the expression level and localization of glial IFN-gamma receptors (IFN-gamma-R) in the human central nervous system (CNS) is sparse. To examine the glial expression of IFN-gamma-R in the human CNS, immunohistochemistry and quantitative analyses were performed on Alzheimer disease hippocampus, Parkinson disease substantia nigra, amyotrophic lateral sclerosis spinal cord and corresponding areas from non-neurological cases. Almost all IFN-gamma-R-positive (IFN-gamma-R(+)) cells corresponded to GFAP-positive (GFAP(+)) astrocytes, while none of IFN-gamma-R(+) cells corresponded to IBA1-positive (IBA1(+)) microglia or MBP-positive (MBP(+)) oligodendrocytes in these neurological cases. We observed a similar pattern of glial IFN-gamma-R expression in non-neurological cases. Also, we quantitatively analyzed the IFN-gamma-R expression by cultured human glial cells using immunocytochemistry and reverse transcription polymerase chain reaction (RT-PCR). In contrast to in vivo results, almost all IFN-gamma-R(+) cells were IBA1(+) in microglial cultures, GFAP(+) in astrocytic cultures and MBP(+) in oligodendrocytic cultures. Moreover, no significant difference in IFN-gamma-R mRNA expression was found for these glial cell types by RT-PCR. These results suggest that the microglial and oligodendrocytic expression levels of IFN-gamma-R are much lower than the astrocytic expression levels in the human CNS in vivo, whereas all three types of glial cells constitutively express IFN-gamma-R when cultured in vitro.

摘要

尽管干扰素-γ(IFN-γ)对神经胶质细胞的显著作用已有充分的文献记载,但有关其在人类中枢神经系统(CNS)中的表达水平和定位的信息却很少。为了研究 IFN-γ-R 在人类中枢神经系统中的神经胶质表达,我们对阿尔茨海默病海马、帕金森病黑质、肌萎缩侧索硬化症脊髓以及相应的非神经病例进行了免疫组织化学和定量分析。几乎所有 IFN-γ-R 阳性(IFN-γ-R(+))细胞都对应于 GFAP 阳性(GFAP(+))星形胶质细胞,而在这些神经病例中,没有任何 IFN-γ-R(+)细胞对应于 IBA1 阳性(IBA1(+))小胶质细胞或 MBP 阳性(MBP(+))少突胶质细胞。我们在非神经病例中观察到类似的神经胶质 IFN-γ-R 表达模式。此外,我们还通过免疫细胞化学和逆转录聚合酶链反应(RT-PCR)定量分析了培养的人类神经胶质细胞中的 IFN-γ-R 表达。与体内结果相反,在小胶质细胞培养物中,几乎所有 IFN-γ-R(+)细胞都是 IBA1(+),在星形胶质细胞培养物中是 GFAP(+),在少突胶质细胞培养物中是 MBP(+)。此外,通过 RT-PCR 发现这三种神经胶质细胞类型的 IFN-γ-R mRNA 表达没有显著差异。这些结果表明,在人类中枢神经系统中,与体内的星形胶质细胞表达水平相比,小胶质细胞和少突胶质细胞中 IFN-γ-R 的表达水平要低得多,而当在体外培养时,所有三种类型的神经胶质细胞都能持续表达 IFN-γ-R。

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