Kouwenhoven Arlette, Minassian Violette Der, Marsh Jon W
Section on Directed Gene Transfer, Laboratory of Cellular and Molecular Regulation, NIMH, Bethesda, MD 20892-4483, USA.
Curr HIV Res. 2013 Apr;11(3):198-209. doi: 10.2174/1570162x113119990039.
The HIV-1 Nef protein brings about increased T cell activity and viral titers through mechanisms that are poorly understood. Nef activity has been described as an enhancer, but not an inducer, of certain signaling pathways that lead to T cell activation and viral production, particularly from resting T cells. The protein has also been found to associate with and promote autophosphorylation of a serine kinase, Pak2, but the Nef-associated kinase level is very low and difficult to study. Here we demonstrate that Nef expression mediates phosphorylation of Mek1 serine298 in T cell lines as well as primary human T cells, thus directly affecting the Erk cascade. This phosphorylation is through a Pak and Rac activity. We also find that Pak2 in Nef expressing cells is phosphorylated on serine192/197, the first biochemical description of the Nef-mediated activation state for this kinase.
人类免疫缺陷病毒1型(HIV-1)的Nef蛋白通过一些尚未完全了解的机制导致T细胞活性增加和病毒滴度升高。Nef的活性被描述为某些导致T细胞活化和病毒产生的信号通路的增强剂,而非诱导剂,尤其是在静息T细胞中。该蛋白还被发现与丝氨酸激酶Pak2结合并促进其自身磷酸化,但与Nef相关的激酶水平非常低且难以研究。在这里,我们证明Nef的表达介导了T细胞系以及原代人T细胞中Mek1丝氨酸298的磷酸化,从而直接影响Erk级联反应。这种磷酸化是通过Pak和Rac活性实现的。我们还发现,表达Nef的细胞中的Pak2在丝氨酸192/197处发生磷酸化,这是对该激酶Nef介导的激活状态的首次生化描述。