Hioe C E, Chien P C, Lu C, Springer T A, Wang X H, Bandres J, Tuen M
New York University School of Medicine and Manhattan VA Medical Center, New York, New York 10010, USA.
J Virol. 2001 Jan;75(2):1077-82. doi: 10.1128/JVI.75.2.1077-1082.2001.
While CD4 and the chemokine receptors are the principal receptors for human immunodeficiency virus (HIV), other cellular proteins, such as LFA-1, are also involved in HIV infection. LFA-1 and its ligands, ICAM-1, ICAM-2, and ICAM-3, can be expressed on the cells infected by HIV, as well as on the HIV virions themselves. To examine the role of LFA-1 expressed on target cells in HIV infection, Jurkat-derived Jbeta2.7 T-cell lines that express either wild-type LFA-1, a constitutively active mutant LFA-1, or no LFA-1 were used. The presence of wild-type LFA-1 enhanced the initial processes of HIV infection, as well as the subsequent replication and transmission from cell to cell. In contrast, the constitutively active LFA-1 mutant failed to promote virus replication and spread, even though this mutant could help HIV enter cells and establish the initial infection. This study clearly demonstrates the contribution of LFA-1 in the different stages of HIV infection. Moreover, not only is LFA-1 expression important for initial HIV-cell interaction, subsequent replication, and transmission, but its activity must also be properly regulated.
虽然CD4和趋化因子受体是人类免疫缺陷病毒(HIV)的主要受体,但其他细胞蛋白,如淋巴细胞功能相关抗原-1(LFA-1),也参与HIV感染。LFA-1及其配体细胞间黏附分子-1(ICAM-1)、ICAM-2和ICAM-3,可在受HIV感染的细胞以及HIV病毒粒子本身表达。为了研究靶细胞上表达的LFA-1在HIV感染中的作用,使用了源自Jurkat的Jbeta2.7 T细胞系,这些细胞系分别表达野生型LFA-1、组成型活性突变体LFA-1或不表达LFA-1。野生型LFA-1的存在增强了HIV感染的初始过程,以及随后的复制和细胞间传播。相反,组成型活性LFA-1突变体未能促进病毒复制和传播,尽管该突变体可帮助HIV进入细胞并建立初始感染。这项研究清楚地证明了LFA-1在HIV感染不同阶段的作用。此外,不仅LFA-1的表达对于HIV与细胞的初始相互作用、随后的复制和传播很重要,其活性也必须得到适当调节。