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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Induction of matrix metalloproteinase-2 in human immunodeficiency virus-1 glycoprotein 120 transgenic mouse brains.
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Induction of matrix metalloproteinase-2 in human immunodeficiency virus-1 glycoprotein 120 transgenic mouse brains.

机译:在人类免疫缺陷病毒1糖蛋白120转基因小鼠大脑中诱导基质金属蛋白酶2。

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摘要

Human immunodeficiency virus (HIV)-1 can invade the brain and cause degeneration of the central nervous system, resulting in a host of cognitive and motor impairments. HIV-1 glycoprotein 120 (gp120), has been implicated in the neurodegenerative effects of HIV infection. Here, gp120's neurotoxic potential is demonstrated in both transgenic mice and cultured cells. We observed that gp120 causes an induction of matrix metalloproteinase (MMP)-2 activity and protein in transgenic mouse brains and in transfected C6 cells. We propose that induced MMP-2 may contribute to a neurodegenerative environment by degrading extracellular matrix (ECM) fibronectin and type IV collagen.
机译:人类免疫缺陷病毒(HIV)-1可以侵入大脑并引起中枢神经系统退化,从而导致许多认知和运动障碍。 HIV-1糖蛋白120(gp120)与HIV感染的神经退行性作用有关。在这里,在转基因小鼠和培养的细胞中均证实了gp120的神经毒性潜力。我们观察到,gp120在转基因小鼠大脑和转染的C6细胞中引起基质金属蛋白酶(MMP)-2活性和蛋白质的诱导。我们建议诱导的MMP-2可能通过降解细胞外基质(ECM)纤连蛋白和IV型胶原蛋白来促进神经退行性环境。

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