González M A, Serrano F, Llorente M, Abad J L, García-Ortiz M J, Bernad A
Department of Immunology and Oncology, Centro Nacional de Biotecnología-CSIC, UAM Campus de Cantoblanco, Madrid, E-28049, Spain.
Biochem Biophys Res Commun. 1998 Oct 20;251(2):592-6. doi: 10.1006/bbrc.1998.9522.
The CCR5 chemokine receptor plays a crucial role in the initiation of in vivo HIV infection, acting as a critical coreceptor molecule for primary strains. Individuals with mutations in the CCR5 gene that reduce its level of expression are resistant to HIV-1 infection. Since these mutations are not associated with any known clinical condition, CCR5 may be an ideal target for anti-HIV therapy. We have designed an artificial hammerhead ribozyme, denoted RzR5-76, targeted to exon 2 of the human CCR5 mRNA. When RzR5-76 activity is induced in HEK 293 cells transfected with a CCR5 expression plasmid, the surface levels of this chemokine receptor are reduced up to 60%. The results indicate that this inhibitory effect is mainly due to the catalytic activity of the ribozyme and not to its antisense properties. These preliminary data suggest that intracellular ribozymes could be used in vivo to block HIV-1 entry into human cells.
CCR5趋化因子受体在体内HIV感染的起始过程中发挥着关键作用,作为主要毒株的关键共受体分子。CCR5基因发生突变从而降低其表达水平的个体对HIV-1感染具有抗性。由于这些突变与任何已知临床病症均无关联,CCR5可能是抗HIV治疗的理想靶点。我们设计了一种人工锤头状核酶,命名为RzR5-76,其靶向人CCR5 mRNA的外显子2。当在转染了CCR5表达质粒的HEK 293细胞中诱导RzR5-76活性时,这种趋化因子受体的表面水平降低了多达60%。结果表明这种抑制作用主要归因于核酶的催化活性而非其反义特性。这些初步数据表明细胞内核酶可在体内用于阻断HIV-1进入人体细胞。