Nef enhances c-Cbl phosphorylation in HIV-infected CD4+ T lymphocytes

被引:14
|
作者
Yang, PL [1 ]
Henderson, AJ [1 ]
机构
[1] Penn State Univ, Dept Vet Sci, Immunol Res Labs, Integrated Biosci Grad Program Immunobiol, University Pk, PA 16802 USA
关键词
HIV-1; Nef; Cbl; T cell signal transduction;
D O I
10.1016/j.virol.2005.03.021
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The multi functional HIV-1 protein Nef possesses several motifs that interact with signaling molecules in infected T cells. In order to determine whether Nef influences T cell activation, cells were infected with Nef-positive and Nef-negative clones of HIV. CD28 expression and changes in tyrosine phosphorylation were monitored. We observed no Nef-dependent changes in CD28 expression or function. However, infection with Nef-positive virus led to changes in tyrosine phosphorylation. This Nef-induced phosphorylation was observed in unstimulated cells, and c-Cbl was identified as one of the proteins whose phosphorylation was upregulated by Nef. Furthermore, Lck is required for Nef-mediated c-Cbl tyrosine phosphorylation. These results suggest that Nef modifies T cell signaling in the absence of T cell receptor engagement and co-stimulation. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:219 / 228
页数:10
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