The HIV Nef Protein Alters Ca2+Signaling in Myelomonocytic Cells through SH3-mediated Protein-Protein Interactions

Michelangelo Foti, Laetitia Cartier, Vincent Piguet, Daniel P. Lew, Jean-Louis Carpentier, Didier Trono, Karl-Heinz Krause
1999 Journal of Biological Chemistry  
Human immunodeficiency virus Nef plays an important role in AIDS pathogenesis. In addition to the well known down-regulation of cell surface receptors (CD4, MHCI), Nef is able to alter cellular signaling. Of particular interest for this study is the ability of Nef to bind with a very high affinity to SH3 domains of myelomonocyte-specific protein-tyrosine kinases of the Src family (Src-like PTK). We have therefore investigated Ca 2؉ signaling in HL60 cells retrovirally transduced with wild type
more » ... ced with wild type Nef or with a Nef mutant deficient in the SH3interacting proline-rich motif (Nef (PXXP)4 ؊). In differentiated HL60 cells, Nef markedly altered cellular Ca 2؉ signaling; the amount of intracellularly stored Ca 2؉ was increased, and as a consequence, store-operated Ca 2؉influx was decreased. This effect was not observed in undifferentiated HL60 cells or in CEM T-lymphocytes and correlated with the differentiation-induced up-regulation of Src-like PTK. The Nef effect on Ca 2؉ signaling depended entirely on the integrity of its PXXP motif. The Src-like PTK p56/59 hck co-immunoprecipitated with both Nef and with the inositol 1,4,5-trisphosphate receptor, providing a possible mechanistic link between the viral protein and intracellular Ca 2؉ stores of the host cell. Collectively, our results demonstrate that the human immunodeficiency virus 1 Nef protein manipulates intracellular Ca 2؉ stores through SH3-mediated interactions in myelomonocytic cells.
doi:10.1074/jbc.274.49.34765 pmid:10574946 fatcat:runi4umu2jejha3onivql2mf3u