Level of ICAM-1 surface expression on virus producer cells influences both the amount of virion-bound host ICAM-1 and human immunodeficiency virus type 1 infectivity
被引:58
作者:
Paquette, JS
论文数: 0引用数: 0
h-index: 0
机构:CHU Laval, Unite Immunoretrovirol Humaine, Ctr Rech Infectiol, Quebec City, PQ G1V 4G2, Canada
Paquette, JS
Fortin, JF
论文数: 0引用数: 0
h-index: 0
机构:CHU Laval, Unite Immunoretrovirol Humaine, Ctr Rech Infectiol, Quebec City, PQ G1V 4G2, Canada
Fortin, JF
Blanchard, L
论文数: 0引用数: 0
h-index: 0
机构:CHU Laval, Unite Immunoretrovirol Humaine, Ctr Rech Infectiol, Quebec City, PQ G1V 4G2, Canada
Blanchard, L
Tremblay, MJ
论文数: 0引用数: 0
h-index: 0
机构:CHU Laval, Unite Immunoretrovirol Humaine, Ctr Rech Infectiol, Quebec City, PQ G1V 4G2, Canada
Tremblay, MJ
机构:
[1] CHU Laval, Unite Immunoretrovirol Humaine, Ctr Rech Infectiol, Quebec City, PQ G1V 4G2, Canada
[2] Univ Laval, Fac Med, Dept Med Biol, Quebec City, PQ G1V 4G2, Canada
Using virions harvested from 293T cells stably expressing either low or high levels of surface ICAM-1, we determined that the number of virus-embedded host ICAM-1 I proteins is positively influenced by the expression level of ICAM-1 on virus producer cells. Moreover, the increase in virion-bound host cell membrane ICAM-1 led to a concomitant enhancement of virus infectivity when a T-cell-tropic strain of human immunodeficiency virus type I (HIV-1) was used. The phenomenon was also seen when primary human cells were infected with virions pseudotyped with the envelope protein from a macrophage-tropic HIV-I isolate, thus ruling out any envelope-specific effect, We also observed that target cells treated with NKI-L16, an anti-LFA-l antibody known to increase the affinity of LFA-1 for ICAM-1, were markedly more susceptible to infection with HIV-1 particles bearing on their surfaces large numbers of host-derived ICAM-1 proteins. Given that cellular activation of leukocytes is known to modify the conformational state of LFA-I and induce ICAM-1 surface expression, it is tempting to speculate that activation of virus infected cells will lead to the production of HIV-I particles bearing more host ICAM-1 on their surfaces and that such progeny virions will preferentially infect and replicate more efficiently in activated cells which are prevalent in lymphoid organs.