首页> 外文期刊>European journal of neurology: the official journal of the European Federation of Neurological Societies >Gelatinolytic activity of matrix metalloproteinase-2 and matrix metalloproteinase-9 in rat brain after implantation of 9L rat glioma cells.
【24h】

Gelatinolytic activity of matrix metalloproteinase-2 and matrix metalloproteinase-9 in rat brain after implantation of 9L rat glioma cells.

机译:9L大鼠神经胶质瘤细胞植入后基质金属蛋白酶2和基质金属蛋白酶9在大鼠脑中的明胶分解活性。

获取原文
获取原文并翻译 | 示例
           

摘要

The matrix metalloproteinases (MMPs) have come to be highlighted by their close relation to the cell invasion of gliomas. The inhibitors of MMPs have undergone extensive development because of its effectiveness against tumor invasion and angiogenesis. Therefore, a suitable animal model is necessary for searching new MMPs inhibitors against gliomas. In this study, we established an experimental model by implanting 9L glioma cells stereotactically into Fisher344 (F344) rat's brain, and the expression and enzymatic activity of MMP-2 and MMP-9 in 9L glioma cells and in tumor tissue was determined by means of reverse transcription polymerase chain reaction (RT-PCR), sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) zymography, in situ film zymography and immunostaining. The results of RT-PCR showed that the mRNA level of MMP-2 in 9L glioma cells was higher than that of MMP-9, and the mRNA expression of MMP-9 was increased along with the growth of malignant gliomas. SDS-PAGE zymography revealed that the expression of MMP-2 and MMP-9 were significantly increased in tumor tissues, and the MMP-9 wasn't detected in normal tissue. The positive stain of MMP-2 and MMP-9 was enhanced with the growth of malignant gliomas, especially for MMP-9. The expression of active gelatinase was found in tumor tissue. In conclusion, the expression of active MMP-2 and MMP-9 was increased in 9L/F344 rat brain during the growth of malignant gliomas at different time intervals, which indicate that 9L/F344 animal model may be a prospective animal model to test new MMPs inhibitors.
机译:基质金属蛋白酶(MMP)与神经胶质瘤的细胞侵袭密切相关。 MMP的抑制剂由于其抗肿瘤侵袭和血管生成的功效而经历了广泛的发展。因此,寻找新的针对神经胶质瘤的MMPs抑制剂的合适动物模型是必要的。在这项研究中,我们建立了将9L胶质瘤细胞立体定向植入Fisher344(F344)大鼠大脑的实验模型,并通过以下方法确定了9L胶质瘤细胞和肿瘤组织中MMP-2和MMP-9的表达和酶活性。逆转录聚合酶链反应(RT-PCR),十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)酶谱,原位膜酶谱和免疫染色。 RT-PCR结果显示9L神经胶质瘤细胞中MMP-2的mRNA水平高于MMP-9,并且随着恶性神经胶质瘤的生长MMP-9的mRNA表达增加。 SDS-PAGE酶谱分析表明,肿瘤组织中MMP-2和MMP-9的表达明显升高,而正常组织中未检测到MMP-9。 MMP-2和MMP-9的阳性染色随着恶性神经胶质瘤的生长而增强,特别是对于MMP-9。在肿瘤组织中发现了活性明胶酶的表达。总之,在不同时间间隔的恶性神经胶质瘤生长过程中,9L / F344大鼠脑中活性MMP-2和MMP-9的表达增加,这表明9L / F344动物模型可能是测试新动物的前瞻性动物模型。 MMPs抑制剂。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号