Abstract
Since some murine cells expressing human CD4 fail to internalize HIV-1, another block was thought to be located at the level of viral entry in addition to CD4. Recently, CXCR4 was shown to function as a coreceptor for T cell line-tropic HIV-1 entry. Here we demonstrated that cells expressing murine CXCR4 and human CD4 fused with cells expressing the env proteins derived from T cell line-tropic HIV-1 and were infected with T cell line-tropic HIV-1 strains. In contrast, the same cells were not infected with chimeric clones constructed by substitution of monocyte- or macrophage-tropic strain-derived env region or V3 region into T cell line-tropic HIV-1, indicating V3 loop of envelope protein is required for murine CXCR4mediated HIV-1 entry. We conclude that murine CXCR4 is not a species specific barrier to the entry of T cell line-tropic HIV-1.
MeSH Terms
3T3 Cells
Animals
CD4 Antigens/biosynthesis,physiology
Calcium/metabolism
Cell Fusion
DNA Primers
GTP-Binding Proteins/physiology
Gene Products, env/biosynthesis
HIV-1/pathogenicity,physiology
Humans
Membrane Proteins/biosynthesis,physiology
Mice
Polymerase Chain Reaction
Receptors, CXCR4
Receptors, HIV/biosynthesis,physiology
Recombinant Fusion Proteins/metabolism
T-Lymphocytes
Transfection
Chemicals
CD4 Antigens
DNA Primers
Gene Products, env
Membrane Proteins
Receptors, CXCR4
Receptors, HIV
Recombinant Fusion Proteins
GTP-Binding Proteins
Calcium
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Tachibana K
Department of Immunology, Research Institute, Osaka Medical Center for Maternal and Child Health, Osaka 590-02, Japan.
Nakajima T
Sato A
Igarashi K
Shida H
Iizasa H
Yoshida N
Yoshie O
Kishimoto T
Nagasawa T
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