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首页> 外文期刊>Experimental & molecular medicine. >Extracellular HIV-1 Tat up-regulates expression of matrix metalloproteinase-9 via a MAPK-NF-κB dependent pathway in human astrocytes
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Extracellular HIV-1 Tat up-regulates expression of matrix metalloproteinase-9 via a MAPK-NF-κB dependent pathway in human astrocytes

机译:细胞外HIV-1 Tat通过人类星形胶质细胞中MAPK-NF-κB依赖性途径上调基质金属蛋白酶9的表达

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The infiltration of monocytes into the CNS represents one of the early steps to inflammatory events in AIDS-related encephalitis and dementia. Increased activity of selected matrix metalloproteinases (MMPs) such as MMP-9 impairs the integrity of blood-brain barrier leading to enhanced monocyte infiltration into the CNS. In this study, we examined the effect of HIV-1 Tat on the expression of MMP-9 in CRT-MG human astroglioma cells. Treatment of CRT-MG cells with HIV-1 Tat protein significantly increased protein levels of MMP-9, as measured by Western blot analysis, zymography and an ELISA. Treatment of CRT-MG cells with HIV-1 Tat protein markedly increased mRNA levels of MMP-9, as analyzed by RT-PCR. Pretreatment of CRT-MG cells with NF-κB inhibitors led to decrease in Tat-induced protein and mRNA expression of MMP-9. Pretreatment of CRT-MG cells with MAPK inhibitors suppressed Tat-induced MMP-9 expression. Furthermore, HIV-1 Tat-induced expression of MMP-9 was significantly inhibited by neutralization of TNF-α, but not IL-1β and IL-6. Taken together, our results indicate that HIV-1 Tat can up-regulate expression of MMP-9 via MAPK-NF-κB-dependent mechanisms as well as Tat-induced TNF-α production in astrocytes.
机译:单核细胞向CNS的浸润代表了AIDS相关脑炎和痴呆中炎症事件的早期步骤之一。选定的基质金属蛋白酶(MMPs)(例如MMP-9)活性增强会损害血脑屏障的完整性,从而导致单核细胞向CNS的浸润增强。在这项研究中,我们检查了HIV-1 Tat对CRT-MG人星形胶质瘤细胞中MMP-9表达的影响。通过Western印迹分析,酶谱分析和ELISA测定,用HIV-1 Tat蛋白处理CRT-MG细胞可显着提高MMP-9的蛋白水平。通过RT-PCR分析,用HIV-1 Tat蛋白处理CRT-MG细胞可显着提高MMP-9的mRNA水平。用NF-κB抑制剂预处理CRT-MG细胞导致Tat诱导的MMP-9蛋白和mRNA表达下降。用MAPK抑制剂预处理CRT-MG细胞可抑制Tat诱导的MMP-9表达。此外,TNF-1的中和作用可显着抑制HIV-1 Tat诱导的MMP-9的表达,但IL-1β和IL-6的作用不受抑制。两者合计,我们的结果表明,HIV-1 Tat可以通过MAPK-NF-κB依赖性机制以及星形胶质细胞中Tat诱导的TNF-α产生来上调MMP-9的表达。

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