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Journal of Virology, January 2001, p. 439-447, Vol. 75, No. 1
0022-538X/01/$04.00+0   DOI: 10.1128/JVI.75.1.439-447.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

CXCR4 Is Down-Regulated in Cells Infected with the CD4-Independent X4 Human Immunodeficiency Virus Type 1 Isolate m7NDK

Susana T. Valente,1,* Chantal Chanel,1,2 Julie Dumonceaux,1 René Olivier,3 Stephano Marullo,4 Pascale Briand,1 and Uriel Hazan1,2

INSERM Unité 380 Laboratoire de Pathologie et Genétique Expérimentales, Institut Cochin de Génétique Moléculaire, 75014 Paris,1 Unité d'Oncologie Virale, Institut Pasteur, 75015 Paris,3 Unité UPRES A-8068, Centre National de la Recherche Scientifique, 75014 Paris,4 and UFR de Biochimie, Université de Paris VII-Denis Diderot, 75251 Paris,2 France

Received 24 May 2000/Accepted 29 September 2000

Macrophages and T cells infected in vitro with CD4-dependent human immunodeficiency virus type 1 (HIV-1) isolates have reduced levels of CD4 protein, a phenomenon involved in retroviral interference. We have previously characterized the first CD4-independent HIV-1 X4 isolate m7NDK, which directly interacts with CXCR4 through its mutated gp120. We thus investigate CXCR4 expression in cells infected with this m7NDK CXCR4-dependent HIV-1 mutant. We present evidence of the down-regulation of CXCR4 membrane expression in CD4-positive or -negative cells chronically infected with the HIV-1 m7NDK, a phenomenon which is not observed in the CD4-dependent HIV-1 NDK parental strain. This down-regulation of CXCR4 was demonstrated by fluorescence-activated cell sorter analysis and was confirmed by the absence of CXCR4 functionality in m7NDK-infected cells, independently of the presence of CD4 protein. Furthermore, a drastic reduction of the intracellular level of CXCR4 protein was also observed. Reduced levels of CXCR4 mRNA transcripts were found in m7NDK-infected HeLa and CEM cells, reduced levels that could not be attributed to a reduced stability of CXCR4 mRNA. Down-regulation of CXCR4 on m7NDK-infected cells may thus be explained by transcriptional regulation.


* Corresponding author. Mailing address: INSERM Unité 380 Laboratoire de Pathologie et Genétique Expérimentales, Institut Cochin de Genétique Moléculaire, 22 Rue Méchain, 75014 Paris, France. Phone: 33-1-40516484. Fax: 33-1-40516407. E-mail: valente{at}cochin.inserm.fr.


Journal of Virology, January 2001, p. 439-447, Vol. 75, No. 1
0022-538X/01/$04.00+0   DOI: 10.1128/JVI.75.1.439-447.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



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