HIV-1 Nef mediates Pak phosphorylation of Mek1 serine298 and elicits an active phospho-state of Pak2

Curr HIV Res. 2013 Apr;11(3):198-209. doi: 10.2174/1570162x113119990039.

Abstract

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.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Cells, Cultured
  • HIV-1 / physiology*
  • Host-Pathogen Interactions*
  • Humans
  • MAP Kinase Kinase 1 / metabolism*
  • Phosphorylation
  • Protein Processing, Post-Translational
  • T-Lymphocytes / enzymology
  • T-Lymphocytes / virology
  • nef Gene Products, Human Immunodeficiency Virus / metabolism*
  • p21-Activated Kinases / metabolism*

Substances

  • nef Gene Products, Human Immunodeficiency Virus
  • nef protein, Human immunodeficiency virus 1
  • PAK2 protein, human
  • p21-Activated Kinases
  • MAP Kinase Kinase 1
  • MAP2K1 protein, human