Anzinger Joshua J, Mezo Isaac, Ji Xin, Gabali Ali M, Thomas Larry L, Spear Gregory T
Department of Immunology and Microbiology, Rush University Medical Center, 1735 W. Harrison St., Cohn Building, Chicago, IL 60612, USA.
Virus Res. 2006 Dec;122(1-2):183-8. doi: 10.1016/j.virusres.2006.06.006. Epub 2006 Jul 13.
Strategies that prevent initial HIV infection of cells are greatly needed. In this study, we determined the requirement of divalent cations for HIV infection of and attachment to peripheral blood mononuclear cells (PBMC), which contain several types of HIV-infectable cells-CD4(+) T cells, monocytes and dendritic cells. EDTA, added only during PBMC exposure to HIV, reduced infection by an average of 92%. The reduction of infection by EDTA was accompanied by a reduction in HIV binding to PBMC; R5, X4 and dual-tropic HIV binding to PBMC were inhibited by >85%. EGTA similarly reduced HIV binding to PBMC, while addition of Ca(2+) or Mn(2+), but not Mg(2+), fully restored binding. Virus attachment was inhibited in a dose-dependent manner by trypsin treatment of PBMC, indicating protein involvement in HIV binding. In contrast, mannan or soluble ICAM-1 did not inhibit HIV binding to PBMC. These data indicate that a Ca(2+)-dependent cell-surface protein(s) is responsible for the majority of HIV attachment to and infection of PBMC. Further studies of this are likely to reveal novel strategies to prevent infection of PBMC.
非常需要能够预防细胞初始感染HIV的策略。在本研究中,我们确定了二价阳离子对于HIV感染外周血单核细胞(PBMC)以及与之结合的必要性,PBMC包含多种可被HIV感染的细胞——CD4(+) T细胞、单核细胞和树突状细胞。仅在PBMC暴露于HIV期间添加的EDTA,使感染平均降低了92%。EDTA导致的感染减少伴随着HIV与PBMC结合的减少;R5、X4和双嗜性HIV与PBMC的结合被抑制了85%以上。EGTA同样减少了HIV与PBMC的结合,而添加Ca(2+)或Mn(2+)(而非Mg(2+))可完全恢复结合。用胰蛋白酶处理PBMC以剂量依赖性方式抑制病毒结合,表明蛋白质参与HIV结合。相反,甘露聚糖或可溶性ICAM-1不抑制HIV与PBMC的结合。这些数据表明,一种依赖Ca(2+)的细胞表面蛋白负责大部分HIV与PBMC的结合及感染。对此进行进一步研究可能会揭示预防PBMC感染的新策略。