HIV-1 entry into CD4 + cells is mediated by the chemokine receptor CC-CKR-5
The β-chemokines MIP-1α, MIP-1β and RANTES inhibit infection of CD4 + cells by primary, non-syncytium-inducing (NSI) HIV-1 strains at the virus entry stage, and also block env -mediated cell–cell membrane fusion. CD4 + T cells from some HIV-1-exposed uninfected individuals cannot fuse with NSI HIV-1...
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Veröffentlicht in: | Nature (London) 1996-06, Vol.381 (6584), p.667-673 |
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Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The β-chemokines MIP-1α, MIP-1β and RANTES inhibit infection of CD4
+
cells by primary, non-syncytium-inducing (NSI) HIV-1 strains at the virus entry stage, and also block
env
-mediated cell–cell membrane fusion. CD4
+
T cells from some HIV-1-exposed uninfected individuals cannot fuse with NSI HIV-1 strains and secrete high levels of β-chemokines. Expression of the β-chemokine receptor CC-CKR-5 in CD4
+
, non-permissive human and non-human cells renders them susceptible to infection by NSI strains, and allows
env
-mediated membrane fusion. CC-CKR-5 is a second receptor for NSI primary viruses. |
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ISSN: | 0028-0836 1476-4687 |
DOI: | 10.1038/381667a0 |