MYCOBACTERIUM TUBERCULOSIS STRAIN H37RV INFECTION TOWARDS MATRIX METALLOPROTEINASE (MMP)-2 IN BRAIN

K. Hartono, Prasetyo Adi, D. Hidayati
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引用次数: 0

Abstract

Background. Tuberculous infection in brain can cause microglia to secrete inflammatory factors like  Tumor Necrosis Factor alpha (TNF-α) and Interleukin 1 beta (IL-1β) which will be shown as body immune  respons. Those inflammatory factors eventually can trigger microglia to secrete Matrix Metalloproteinase- 2 (MMP-2) which will regenerate necrotic or apoptosis cells because of inflammation process. MMP-2 has  been proven to have important role in brain tuberculous infection. Objective. To ascertain MMP-2 expression in mus musculus brain tissue with no infection, infection for 8 weeks, and infection for 16 weeks. Methods. This research used semiquantitative method to compare MMP-2 expression in 3 samples group. Observation of MMP-2 expression in mus musculus brain tissue were made by using immunohistochemistry colouration method which then would be observed in microscope with 400x magnification. Brain cell which express MMP-2 will become brown in cell nucleus, cytoplasm, and wall. Results. The result which had be obtained was overtime reduction of MMP-2 expression. Conclusion. MMP-2 expression didn’t decrease after 8 weeks time of infection.
结核分枝杆菌H37RV对脑基质金属蛋白酶(MMP)-2的感染
背景脑结核性感染可引起小胶质细胞分泌肿瘤坏死因子α(TNF-α)和白细胞介素1β(IL-1β)等炎症因子,表现为机体免疫反应。这些炎症因子最终可以触发小胶质细胞分泌基质金属蛋白酶-2(MMP-2),后者会在炎症过程中再生坏死或凋亡的细胞。MMP-2已被证明在脑结核感染中具有重要作用。客观的确定MMP-2在无感染、感染8周和感染16周的脑肌肉组织中的表达。方法。本研究采用半定量方法比较了3个样本组MMP-2的表达情况。用免疫组化染色法观察脑肌肉组织中MMP-2的表达,并在400倍放大显微镜下观察。表达MMP-2的脑细胞会在细胞核、细胞质和细胞壁中变成棕色。后果所获得的结果是MMP-2表达的超时减少。结论MMP-2的表达在感染8周后没有下降。
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