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Phosphatidylinositol-(4,5)-bisphosphate enables efficient secretion of HIV-1 Tat by infected T-cells
by
Roy, Christian
, Rayne, Fabienne
, Debaisieux, Solène
, Konate, Karidia
, Pugnière, Martine
, Bonhoure, Anne
, Sanchez, Françoise
, Beaumelle, Bruno
, Arold, Stefan T
, Lin, Yea‐Lih
, Mettling, Clément
, Briant, Laurence
, Loret, Erwann
, Yezid, Hocine
, Chazal, Nathalie
in
Binding Sites
/ CD4-Positive T-Lymphocytes - metabolism
/ CD4-Positive T-Lymphocytes - virology
/ Cell Membrane - metabolism
/ Cellular biology
/ EMBO20
/ EMBO23
/ Enzyme-Linked Immunosorbent Assay
/ HIV
/ HIV-1
/ HIV-1 - growth & development
/ HIV-1 - pathogenicity
/ Human immunodeficiency virus
/ Human immunodeficiency virus 1
/ Humans
/ Jurkat Cells
/ Life Sciences
/ Life span
/ Membranes
/ Microbiology and Parasitology
/ Molecular biology
/ Phosphatidylinositol 4,5-Diphosphate - metabolism
/ PIP2
/ Protein Binding
/ Proteins
/ Tat
/ tat Gene Products, Human Immunodeficiency Virus - analysis
/ tat Gene Products, Human Immunodeficiency Virus - metabolism
/ toxin
/ unconventional secretion
/ Virology
2010
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Phosphatidylinositol-(4,5)-bisphosphate enables efficient secretion of HIV-1 Tat by infected T-cells
by
Roy, Christian
, Rayne, Fabienne
, Debaisieux, Solène
, Konate, Karidia
, Pugnière, Martine
, Bonhoure, Anne
, Sanchez, Françoise
, Beaumelle, Bruno
, Arold, Stefan T
, Lin, Yea‐Lih
, Mettling, Clément
, Briant, Laurence
, Loret, Erwann
, Yezid, Hocine
, Chazal, Nathalie
in
Binding Sites
/ CD4-Positive T-Lymphocytes - metabolism
/ CD4-Positive T-Lymphocytes - virology
/ Cell Membrane - metabolism
/ Cellular biology
/ EMBO20
/ EMBO23
/ Enzyme-Linked Immunosorbent Assay
/ HIV
/ HIV-1
/ HIV-1 - growth & development
/ HIV-1 - pathogenicity
/ Human immunodeficiency virus
/ Human immunodeficiency virus 1
/ Humans
/ Jurkat Cells
/ Life Sciences
/ Life span
/ Membranes
/ Microbiology and Parasitology
/ Molecular biology
/ Phosphatidylinositol 4,5-Diphosphate - metabolism
/ PIP2
/ Protein Binding
/ Proteins
/ Tat
/ tat Gene Products, Human Immunodeficiency Virus - analysis
/ tat Gene Products, Human Immunodeficiency Virus - metabolism
/ toxin
/ unconventional secretion
/ Virology
2010
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Phosphatidylinositol-(4,5)-bisphosphate enables efficient secretion of HIV-1 Tat by infected T-cells
by
Roy, Christian
, Rayne, Fabienne
, Debaisieux, Solène
, Konate, Karidia
, Pugnière, Martine
, Bonhoure, Anne
, Sanchez, Françoise
, Beaumelle, Bruno
, Arold, Stefan T
, Lin, Yea‐Lih
, Mettling, Clément
, Briant, Laurence
, Loret, Erwann
, Yezid, Hocine
, Chazal, Nathalie
in
Binding Sites
/ CD4-Positive T-Lymphocytes - metabolism
/ CD4-Positive T-Lymphocytes - virology
/ Cell Membrane - metabolism
/ Cellular biology
/ EMBO20
/ EMBO23
/ Enzyme-Linked Immunosorbent Assay
/ HIV
/ HIV-1
/ HIV-1 - growth & development
/ HIV-1 - pathogenicity
/ Human immunodeficiency virus
/ Human immunodeficiency virus 1
/ Humans
/ Jurkat Cells
/ Life Sciences
/ Life span
/ Membranes
/ Microbiology and Parasitology
/ Molecular biology
/ Phosphatidylinositol 4,5-Diphosphate - metabolism
/ PIP2
/ Protein Binding
/ Proteins
/ Tat
/ tat Gene Products, Human Immunodeficiency Virus - analysis
/ tat Gene Products, Human Immunodeficiency Virus - metabolism
/ toxin
/ unconventional secretion
/ Virology
2010
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Phosphatidylinositol-(4,5)-bisphosphate enables efficient secretion of HIV-1 Tat by infected T-cells
Journal Article
Phosphatidylinositol-(4,5)-bisphosphate enables efficient secretion of HIV-1 Tat by infected T-cells
2010
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Overview
Human immunodeficiency virus type 1 (HIV‐1) transcription relies on its transactivating Tat protein. Although devoid of a signal sequence, Tat is released by infected cells and secreted Tat can affect uninfected cells, thereby contributing to HIV‐1 pathogenesis. The mechanism and the efficiency of Tat export remained to be documented. Here, we show that, in HIV‐1‐infected primary CD4
+
T‐cells that are the main targets of the virus, Tat accumulates at the plasma membrane because of its specific binding to phosphatidylinositol‐4,5‐bisphosphate (PI(4,5)P
2
). This interaction is driven by a specific motif of the Tat basic domain that recognizes a single PI(4,5)P
2
molecule and is stabilized by membrane insertion of Tat tryptophan side chain. This original recognition mechanism enables binding to membrane‐embedded PI(4,5)P
2
only, but with an unusually high affinity that allows Tat to perturb the PI(4,5)P
2
‐mediated recruitment of cellular proteins. Tat–PI(4,5)P
2
interaction is strictly required for Tat secretion, a process that is very efficient, as ∼2/3 of Tat are exported by HIV‐1‐infected cells during their lifespan. The function of extracellular Tat in HIV‐1 infection might thus be more significant than earlier thought.
Publisher
John Wiley & Sons, Ltd,Nature Publishing Group UK,Springer Nature B.V,EMBO Press,Nature Publishing Group
Subject
/ CD4-Positive T-Lymphocytes - metabolism
/ CD4-Positive T-Lymphocytes - virology
/ EMBO20
/ EMBO23
/ Enzyme-Linked Immunosorbent Assay
/ HIV
/ HIV-1
/ HIV-1 - growth & development
/ Human immunodeficiency virus
/ Human immunodeficiency virus 1
/ Humans
/ Microbiology and Parasitology
/ Phosphatidylinositol 4,5-Diphosphate - metabolism
/ PIP2
/ Proteins
/ Tat
/ tat Gene Products, Human Immunodeficiency Virus - analysis
/ tat Gene Products, Human Immunodeficiency Virus - metabolism
/ toxin
/ Virology
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