LFA-1 expression on target cells promotes human immunodeficiency virus type 1 infection and transmission

被引:64
作者
Hioe, CE
Chien, PC
Lu, CF
Springer, TA
Wang, XH
Bandres, J
Tuen, M
机构
[1] Vet Adm Med Ctr, Res Serv, New York, NY 10010 USA
[2] NYU, Sch Med, New York, NY 10010 USA
[3] Ctr Blood Res, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA 02115 USA
关键词
D O I
10.1128/JVI.75.2.1077-1082.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
While CD4 and the chemokine receptors are the principal receptors for human immunodeficiency virus (HN), other cellular proteins, such as LFA-1, are also involved in HIV infection. LFA-1 end 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 J beta2.7 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-T in the different stages of HIV infection. Moreover, not only is LFA-1 expression important for initial HN-cell interaction, subsequent replication, and transmission, but its activity must also be properly regulated.
引用
收藏
页码:1077 / 1082
页数:6
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