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J. Biol. Chem., Vol. 276, Issue 12, 8639-8642, March 23, 2001
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and
§
From the Laboratory of Immunoregulation, NIAID, National
Institutes of Health, Bethesda, Maryland 20892 and the Division
of Medical Virology, Department of Molecular Microbiology and
Immunology, Nagasaki University Graduate School of Medical Sciences,
Nagasaki 852-8523, Japan
T cell activation can induce expression of CCR5,
a major coreceptor for macrophage-tropic (R5) human immunodeficiency
virus type 1 (HIV-1). Here we report that overexpression of the Oct-2 transcription factor and octamer coactivator BOB.1/OBF/OCA-B, both of
which are induced in T cells following T cell receptor signaling,
synergistically up-regulates CCR5 promoter activity via interaction
with an octamer motif on the promoter. We also show that the octamer
transcription factors can increase cell surface expression of CCR5 and
fusogenicity of the cells with R5 HIV-1 Env. These results suggest that
octamer transcription factors may play a critical role in the induction
of CCR5 expression on, and thereby susceptibility to, R5 HIV-1 of T
cells following antigenic stimulation.
The two authors contributed equally to this work.
§
To whom correspondence should be addressed: Dept. of Pediatrics,
Nagasaki University School of Medicine, 1-7-1 Sakamoto, Nagasaki 852-8501, Japan. Tel.: 81-95-849-7297; Fax: 81-95-849-7301; E-mail: hiromori@net.nagasaki-u.ac.jp.
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