C6细胞悬液接种成年大鼠脑:免疫组织化学研究。

J Mokrý, S Nĕmecek, J Adler, K Dĕdic
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摘要

将C6胶质瘤细胞悬液接种于成年朗埃文斯大鼠脑内。动物存活2 ~ 60 d后,在石蜡包埋切片上免疫组化检测肿瘤组织中S100蛋白和胶质纤维酸性蛋白(GFAP)。在我们的体内模型中,在植入后10天C6胶质细胞中观察到s100蛋白和GFAP的最高阳性。同时,在含有更多分化的C6胶质瘤细胞的中心区域和肿瘤边界的宿主反应性星形胶质细胞中,s100蛋白的表达水平升高。肿瘤外周及邻近血管周围间隙的C6胶质瘤细胞在分裂和侵袭(即低分化)中几乎没有发现s100蛋白。GFAP阳性细胞的分布与含C6的s100蛋白细胞的分布相似。GFAP表达细胞出现在静止的肿瘤中心部位,该部位被分化程度较高的细胞占据。肿瘤周围有强烈GFAP阳性的宿主反应性星形胶质细胞。随后,当肿瘤消退迹象出现时,C6胶质瘤细胞的s100蛋白和GFAP免疫反应性下降。总之,我们建立了一个体内模型来观察生长中的胶质瘤中的细胞分化。与中心和更安静的肿瘤部分相比,分化程度较低和恶性程度较高的胶质瘤细胞几乎不表达s100蛋白和GFAP。
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Inoculation of C6 cell suspension into the brain of adult rats: immunohistochemical study.

C6 glioma cell suspension has been inoculated into the brain of adult Long Evans rats. Animals were allowed to survive 2 to 60 days and then immunohistochemical detection of S100 protein and glial fibrillary acidic protein (GFAP) in tumors was carried out on paraffin-embedded sections. In our in vivo model the maximum positivity for both S 100 protein and GFAP was observed in C6 glial cells at 10 days after implantation. At that time increased levels of S 100 protein were expressed both in central areas containing more differentiated C6 glioma cells and in host reactive astrocytes at tumor boundary. Almost no S 100 protein was found in dividing and invading, i.e. less differentiated, C6 glioma cells at tumor periphery and in perivascular spaces of adjacent blood vessels. The distribution of GFAP positive cells followed a similar pattern as that of S 100 protein containing C6 cells. GFAP expressing cells were revealed in quiescent central tumor portions which were occupied by more differentiated cells. Tumors were surrounded by strongly GFAP positive host reactive astrocytes. Later on, when signs of tumor regression appeared there was a decrease in S 100 protein and GFAP immunoreactivity of C6 glioma cells. To summarize, we developed an in vivo model for observation of cell differentiation within a growing glioma. Less differentiated and more malignant glioma cells expressed almost no S 100 protein and GFAP in contradistinction to central and more quiescent tumor portions.

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