Suppr超能文献

HIV-1的Tat蛋白刺激艾滋病患者卡波西肉瘤损伤部位来源的细胞生长。

Tat protein of HIV-1 stimulates growth of cells derived from Kaposi's sarcoma lesions of AIDS patients.

作者信息

Ensoli B, Barillari G, Salahuddin S Z, Gallo R C, Wong-Staal F

机构信息

Laboratory of Tumor Cell Biology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

Nature. 1990 May 3;345(6270):84-6. doi: 10.1038/345084a0.

Abstract

Kaposi's sarcoma (KS) is frequently associated with human immunodeficiency virus-1 (HIV-1) infection. Supernatants from HIV-1-infected T cells carrying the CD4 antigen promote the growth of cells derived from KS lesions of AIDS patients (AIDS-KS cells), and the HIV-1 tat gene, introduced into the germ line of mice, induces skin lesions closely resembling KS. Here we report that the tat gene product (Tat) is released from both HIV-1-acutely infected H9 cells and tat-transfected COS-1 cells. These Tat-containing supernatants specifically promote growth of AIDS-KS cells which are inhibited by anti-Tat antibodies; recombinant Tat has the same growth-promoting properties. Therefore a viral regulatory gene product can be released as a biologically active protein and directly act as a growth stimulator. These and previous data indicate that extracellular Tat could be involved in the development or progression, or both, of KS in HIV-1-infected individuals.

摘要

卡波西肉瘤(KS)常与人类免疫缺陷病毒1型(HIV-1)感染相关。携带CD4抗原的HIV-1感染T细胞的上清液可促进艾滋病患者KS病变来源细胞(艾滋病相关卡波西肉瘤细胞)的生长,并且导入小鼠种系的HIV-1 tat基因可诱导出与KS极为相似的皮肤病变。在此我们报告,tat基因产物(Tat)可从HIV-1急性感染的H9细胞和tat转染的COS-1细胞中释放出来。这些含有Tat的上清液可特异性促进艾滋病相关卡波西肉瘤细胞的生长,而抗Tat抗体可抑制该生长;重组Tat具有相同的促生长特性。因此,一种病毒调节基因产物可作为一种生物活性蛋白释放出来,并直接充当生长刺激因子。这些以及先前的数据表明,细胞外Tat可能参与了HIV-1感染个体中KS的发生或发展,或两者兼有。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验