HIV-1 Nef Transfer and Intracellular Signalling in Uninfected Cells. (part 1, Chapter 3)

1. Introduction Several lymphotropic viruses manipulate host innate immune response to escape immune recognition and improve viral replication and spreading. From this point of view HIV (Human Immunodeficiency Virus-1) represents a paradigmatic example (for review see Peterlin & Trono, 2003). HIV-1 encodes the classical structural and enzymatic factors of all retroviruses codified from the gag (group-specific antigen), pol (polymerase) and env (envelope) genes. In addition it codes two regulatory proteins that are essential for viral replication (i.e., the transcriptional transactivator Tat and the regulator of virion gene expression Rev) and four accessory proteins (i.e., the ill-named ‘negative effector’ Nef, the viral infectivity factor Vif, the viral protein r Vpr and the viral protein u Vpu). With time has become increasingly clear that the so-called accessory proteins carry out several critical functions for both viral replication and pathogenesis (Malim & Emerman, 2008). In particular, the Nef protein was demonstrated to be an important virulence factor of primate lentiviruses. In fact Nef-defective HIV leads to an attenuated clinical phenotype with reduced viral loads in mouse models, monkeys, and in human disease (Daniel et al., 1992; Deacon et al., 1995; Gulizia et al., 1997; Kestler et al., 1991; Kirchhoff et al., 1995) and nef transgenic mice develop an AIDS-like disease (Hanna et al., 1998) confirming that this viral protein is a major determinant of pathogenicity. Studies on structure and mechanism of action of the protein highlighted its multifunctional properties at cellular and molecular level. The open reading frame encoding Nef is located 3′ of the env gene, overlaps the untranslated sequences of the 3′ viral long terminal repeat and is translated from multiply spliced transcripts. Nef is expressed early and most abundantly during the infection cycle together with Tat and Rev and evidences have been reported of possible expression also before integration of the proviral genome (Wu & Marsh, 2001). It acts as a molecular adaptor inside the cell inducing genetically distinguishable, yet highly HIV-Host Interactions 62 conserved, effects via specific protein-protein interaction motifs (Arold & Baur, 2001; Doms & Trono, 2000; Geyer et al., 2001, Foster et al., 2011). In general, Nefs from all primate lentiviruses (i.e. HIV-1, HIV-2, and SIV) share multiple activities in vitro, but differences between the ability of human and simian immunodeficiency viruses to induce Nef-mediated internalization of the CD3 component of the T-cell receptor complex have been observed and have been correlated with the greater pathogenicity of HIV and the reduction of T-cell activation in simian immunodeficiency virus (SIV) (Schindler et al., 2006). It has been also observed that HIV-1 Nef treatment of uninfected cells in culture causes internalization of the protein in some cell types and/or activates specific intracellular signalling pathways. Interestingly, Nef has been found inside uninfected B cells of lymphoid follicles from infected individuals (Qiao et al., 2006) and recently it has been provided experimental evidencies that it can be transferred to uninfected cells from the infected ones via cellular protrusions and/or exosomes (Lenassi et al., 2010; Muratori et al., 2009; Xu et al., 2009) opening a new road to deepen our insight on the roles of this multifunctional protein. This review will focus on those recent observations trying to provide a unifying reading.