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表达HIV反式激活因子基因的转基因小鼠中淋巴组织增生的发展

Development of lymphoid hyperplasia in transgenic mice expressing the HIV tat gene.

作者信息

Vellutini C, Horschowski N, Philippon V, Gambarelli D, Nave K A, Filippi P

机构信息

Laboratoire de Virologie, INSERM U372, Marseille, France.

出版信息

AIDS Res Hum Retroviruses. 1995 Jan;11(1):21-9. doi: 10.1089/aid.1995.11.21.

Abstract

During HIV infection, individuals experience multiorgan disorders such as adenopathy, splenomegaly, and lung and brain diseases. There is an increasing body of evidence that the HIV trans-activating tat gene product possesses multiple activities. First, it can activate several cellular genes; second, in its extracellular soluble form, it plays the role of growth factor in some cells such as Kaposi's sarcoma cells. Thus, we introduced the HIV tat gene, under the control of the cellular proteolipoprotein promoter, into the germline of mice and demonstrate that, when expressed, the tat gene product induces lymphoid hyperplasia in spleen, lymph nodes, and lung, as is observed in AIDS patients, but not in the brain or testes. Our findings indicate that HIV, through some of its genes, directly participates in the pathogenesis of AIDS.

摘要

在HIV感染期间,个体经历多器官紊乱,如淋巴结病、脾肿大以及肺部和脑部疾病。越来越多的证据表明,HIV反式激活tat基因产物具有多种活性。首先,它可以激活多个细胞基因;其次,以其细胞外可溶性形式,它在某些细胞(如卡波西肉瘤细胞)中发挥生长因子的作用。因此,我们将受细胞蛋白脂蛋白启动子控制的HIV tat基因导入小鼠种系,并证明当tat基因产物表达时,会在脾脏、淋巴结和肺部诱导淋巴样增生,这与艾滋病患者中观察到的情况相同,但在大脑或睾丸中则不会。我们的研究结果表明,HIV通过其一些基因直接参与艾滋病的发病机制。

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