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P-糖蛋白在人脑胶质瘤毛细血管内皮细胞上的超微结构定位

Ultrastructural localization of P-glycoprotein on capillary endothelial cells in human gliomas.

作者信息

Tanaka Y, Abe Y, Tsugu A, Takamiya Y, Akatsuka A, Tsuruo T, Yamazaki H, Ueyama Y, Sato O, Tamaoki N

机构信息

Department of Neurosurgery, Tokai University School of Medicine, Kanagawa, Japan.

出版信息

Virchows Arch. 1994;425(2):133-8. doi: 10.1007/BF00230349.

Abstract

The P-glycoprotein (P-Gp) encoded by the human multidrug-resistance gene MDR1 has been suggested to play certain roles in the blood-brain barrier (BBB). However, the detailed mechanism of the activity of P-Gp in multidrug-resistance (MDR) remains unclear in human glioma. We examined the localization of P-Gp in human glioma by immunohistochemical (IHC) and immunoelectron microscopic (IEM) methods with anti P-Gp monoclonal antibodies (C219, MRK16). We also examined MDR1 expression in primary glioma and xenografts by reverse transcription-polymerase chain reaction (RT-PCR) with human MDR1-specific primers. The IHC study showed no P-Gp expression on tumour cells but it was present on capillary endothelial cells and IEM analysis showed definitive localization on their luminal surface. MDR1 gene expression was detected in eight primary glioma and three normal brain specimens by RT-PCR, but not in glioma xenografts. The lack of MDR1 expression in these cells appears to be a consequence of the replacement of the original human stroma, including blood vessels, by murine stroma in glioma xenografts. The unique distribution of P-Gp on the capillary blood vessels was confirmed in human glioma by the results of immunohistochemical and molecular biological studies.

摘要

人类多药耐药基因MDR1编码的P-糖蛋白(P-Gp)被认为在血脑屏障(BBB)中发挥一定作用。然而,在人类胶质瘤中,P-Gp在多药耐药(MDR)中的详细作用机制仍不清楚。我们使用抗P-Gp单克隆抗体(C219、MRK16),通过免疫组织化学(IHC)和免疫电子显微镜(IEM)方法检测了P-Gp在人类胶质瘤中的定位。我们还使用人MDR1特异性引物,通过逆转录-聚合酶链反应(RT-PCR)检测了原发性胶质瘤和异种移植瘤中MDR1的表达。免疫组织化学研究显示肿瘤细胞上无P-Gp表达,但在毛细血管内皮细胞上有表达;免疫电子显微镜分析显示其明确位于管腔表面。通过RT-PCR在8例原发性胶质瘤和3例正常脑标本中检测到MDR1基因表达,但在胶质瘤异种移植瘤中未检测到。这些细胞中MDR1表达的缺失似乎是由于胶质瘤异种移植瘤中原始人类基质(包括血管)被鼠基质替代的结果。免疫组织化学和分子生物学研究结果证实了P-Gp在人类胶质瘤毛细血管上的独特分布。

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