Krüger U, Pfeiffer T, Bosch V
Forschungsschwerpunkt Angewandte Tumorvirologie, Deutsches Krebsforschungszentrum, Heidelberg, Germany.
AIDS Res Hum Retroviruses. 1996 Jun 10;12(9):783-92. doi: 10.1089/aid.1996.12.783.
To gain more insight into the processes leading to HIV-1 Env-induced cell death, we aim to coexpress stably wild-type and relevant mutant variants of both HIV-1 Env and human CD4 in lymphocyte cell lines. Here we report on the generation and characterization of several cell lines inducibly or constitutively expressing wild-type or cleavage-defective HIV-1 glycoproteins and human CD4 either singly or in combination. Coexpression of CD4 and wild-type Env led to the formation of multinucleated syncytia, to growth arrest and cell death, effects that all could be prevented by cultivation in the presence of monoclonal antibodies that inhibit cell surface membrane fusion. Cell lines coexpressing CD4 and mutated, noncleavable Env, detectable at the cell surface and still retaining CD4-binding capacity, were not retarded in their growth and cytolysis did not occur. These results indicate that cell lysis requires cell surface interaction of CD4 and gp120/41 and cleavage of gp160 to gp120 and gp41.
为了更深入地了解导致HIV-1包膜糖蛋白(Env)诱导细胞死亡的过程,我们旨在在淋巴细胞系中稳定共表达野生型及相关突变型的HIV-1 Env和人类CD4。在此,我们报告了几种可诱导或组成型表达野生型或裂解缺陷型HIV-1糖蛋白以及单独或组合表达人类CD4的细胞系的产生和特性。CD4与野生型Env的共表达导致多核巨细胞的形成、生长停滞和细胞死亡,而在存在抑制细胞表面膜融合的单克隆抗体的情况下进行培养,所有这些效应均可被阻止。共表达CD4和在细胞表面可检测到且仍保留CD4结合能力的突变型、不可裂解Env的细胞系,其生长未受抑制,也未发生细胞溶解。这些结果表明,细胞裂解需要CD4与gp120/41在细胞表面相互作用以及gp160裂解为gp120和gp41。