Cholesterol contributes to the organization of tetraspanin-enriched microdomains and to CD81-dependent infection by malaria sporozoites
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G. van Gemert | R. Sauerwein | F. Dautry | C. Boucheix | M. Billard | S. Charrin | E. Rubinstein | D. Mazier | Krista L. Clark | O. Silvie | J. Franetich | Stéphanie Charrin
[1] S. Levy,et al. Expression of human CD81 differently affects host cell susceptibility to malaria sporozoites depending on the Plasmodium species , 2006, Cellular microbiology.
[2] Jean Dubuisson,et al. High Density Lipoproteins Facilitate Hepatitis C Virus Entry through the Scavenger Receptor Class B Type I* , 2005, Journal of Biological Chemistry.
[3] Y. Wada,et al. Potentiation of the ligand-binding activity of integrin α3β1 via association with tetraspanin CD151 , 2005 .
[4] S. Levy,et al. The tetraspanin web modulates immune-signalling complexes , 2005, Nature Reviews Immunology.
[5] G. Bismuth,et al. Tetraspanin CD82 controls the association of cholesterol-dependent microdomains with the actin cytoskeleton in T lymphocytes: relevance to co-stimulation , 2004, Journal of Cell Science.
[6] M. Connelly,et al. Scavenger receptor BI: A scavenger receptor with a mission to transport high density lipoprotein lipids , 2004, Current opinion in lipidology.
[7] Krista L. Clark,et al. CD81 Associates with 14-3-3 in a Redox-regulated Palmitoylation-dependent Manner* , 2004, Journal of Biological Chemistry.
[8] Markus S. Mueller,et al. A Role for Apical Membrane Antigen 1 during Invasion of Hepatocytes by Plasmodium falciparum Sporozoites* , 2004, Journal of Biological Chemistry.
[9] C. Rice,et al. CD81 Is Required for Hepatitis C Virus Glycoprotein-Mediated Viral Infection , 2004, Journal of Virology.
[10] R. Alon,et al. The CD81 Tetraspanin Facilitates Instantaneous Leukocyte VLA-4 Adhesion Strengthening to Vascular Cell Adhesion Molecule 1 (VCAM-1) under Shear Flow* , 2003, Journal of Biological Chemistry.
[11] M. Hemler. Tetraspanin proteins mediate cellular penetration, invasion, and fusion events and define a novel type of membrane microdomain. , 2003, Annual review of cell and developmental biology.
[12] E. Odintsova,et al. Tetraspanin CD82 regulates compartmentalisation and ligand-induced dimerization of EGFR , 2003, Journal of Cell Science.
[13] S. Munro. Lipid Rafts Elusive or Illusive? , 2003, Cell.
[14] R. Cortese,et al. Cell Entry of Hepatitis C Virus Requires a Set of Co-receptors That Include the CD81 Tetraspanin and the SR-B1 Scavenger Receptor* , 2003, Journal of Biological Chemistry.
[15] S. Levy,et al. The Tetraspanin CD81 Regulates the Expression of CD19 During B Cell Development in a Postendoplasmic Reticulum Compartment 1 , 2003, The Journal of Immunology.
[16] D. Gerlier,et al. A physical and functional link between cholesterol and tetraspanins , 2003, European journal of immunology.
[17] I. Coppens,et al. Host but not parasite cholesterol controls Toxoplasma cell entry by modulating organelle discharge. , 2003, Molecular biology of the cell.
[18] J. L. Le Caer,et al. EWI-2 is a new component of the tetraspanin web in hepatocytes and lymphoid cells. , 2003, The Biochemical journal.
[19] C. Martínez-A,et al. Pathogens: raft hijackers , 2003, Nature Reviews Immunology.
[20] L. Ashman,et al. Multiple levels of interactions within the tetraspanin web. , 2003, Biochemical and biophysical research communications.
[21] M. Ferguson,et al. Potential Role for CD63 in CCR5-Mediated Human Immunodeficiency Virus Type 1 Infection of Macrophages , 2003, Journal of Virology.
[22] N. Olmo,et al. A Functionally Relevant Conformational Epitope on the CD9 Tetraspanin Depends on the Association with Activated β1Integrin* , 2003, The Journal of Biological Chemistry.
[23] D. Weil,et al. Targeting the kinesin Eg5 to monitor siRNA transfection in mammalian cells. , 2002, BioTechniques.
[24] E. Odintsova,et al. Expression of the Palmitoylation-deficient CD151 Weakens the Association of α3β1 Integrin with the Tetraspanin-enriched Microdomains and Affects Integrin-dependent Signaling* , 2002, The Journal of Biological Chemistry.
[25] M. Hemler,et al. An extracellular site on tetraspanin CD151 determines α3 and α6 integrin–dependent cellular morphology , 2002, The Journal of cell biology.
[26] Kai Simons,et al. Cholesterol, lipid rafts, and disease. , 2002, The Journal of clinical investigation.
[27] Eric Rubinstein,et al. Differential stability of tetraspanin/tetraspanin interactions: role of palmitoylation , 2002, FEBS letters.
[28] W. Eling,et al. Effects of irradiation on Plasmodium falciparum sporozoite hepatic development: implications for the design of pre‐erythrocytic malaria vaccines , 2002, Parasite immunology.
[29] A. Sonnenberg,et al. Association of the tetraspanin CD151 with the laminin-binding integrins alpha3beta1, alpha6beta1, alpha6beta4 and alpha7beta1 in cells in culture and in vivo. , 2002, Journal of cell science.
[30] A. Sonnenberg,et al. Association of the tetraspanin CD151 with the laminin-binding integrinsα 3β1, α6β1, α6β4 and α7β1 in cells in culture and in vivo , 2002 .
[31] J. Kreidberg,et al. Palmitoylation of tetraspanin proteins: modulation of CD151 lateral interactions, subcellular distribution, and integrin-dependent cell morphology. , 2002, Molecular biology of the cell.
[32] T. V. Kolesnikova,et al. EWI-2 Is a Major CD9 and CD81 Partner and Member of a Novel Ig Protein Subfamily* , 2001, The Journal of Biological Chemistry.
[33] Krista L. Clark,et al. PGRL Is a Major CD81-Associated Protein on Lymphocytes and Distinguishes a New Family of Cell Surface Proteins1 , 2001, The Journal of Immunology.
[34] K. Haldar,et al. The Role of Cholesterol and Glycosylphosphatidylinositol-anchored Proteins of Erythrocyte Rafts in Regulating Raft Protein Content and Malarial Infection* , 2001, The Journal of Biological Chemistry.
[35] K. Handa,et al. GM3 ganglioside inhibits CD9-facilitated haptotactic cell motility: coexpression of GM3 and CD9 is essential in the downregulation of tumor cell motility and malignancy. , 2001, Biochemistry.
[36] S. Hanash,et al. The Major CD9 and CD81 Molecular Partner , 2001, The Journal of Biological Chemistry.
[37] M. Hemler,et al. Evaluation of Prototype Transmembrane 4 Superfamily Protein Complexes and Their Relation to Lipid Rafts* , 2001, The Journal of Biological Chemistry.
[38] M. Hemler,et al. FPRP, a Major, Highly Stoichiometric, Highly Specific CD81- and CD9-associated Protein* , 2001, The Journal of Biological Chemistry.
[39] M. Mota,et al. Plasmodium yoelii: efficient in vitro invasion and complete development of sporozoites in mouse hepatic cell lines. , 2000, Experimental parasitology.
[40] K. Haldar,et al. Vacuolar uptake of host components, and a role for cholesterol and sphingomyelin in malarial infection , 2000, The EMBO journal.
[41] C. Jasmin,et al. Severely reduced female fertility in CD9-deficient mice. , 2000, Science.
[42] L. Sibley,et al. Invasion by Toxoplasma gondii Establishes a Moving Junction That Selectively Excludes Host Cell Plasma Membrane Proteins on the Basis of Their Membrane Anchoring , 1999, The Journal of experimental medicine.
[43] E. Brown,et al. Role of Cholesterol in Formation and Function of a Signaling Complex Involving αvβ3, Integrin-Associated Protein (Cd47), and Heterotrimeric G Proteins , 1999, The Journal of cell biology.
[44] B. Baird,et al. Critical Role for Cholesterol in Lyn-mediated Tyrosine Phosphorylation of FcεRI and Their Association with Detergent-resistant Membranes , 1999, The Journal of cell biology.
[45] D. Azorsa,et al. Selective tetraspan-integrin complexes (CD81/alpha4beta1, CD151/alpha3beta1, CD151/alpha6beta1) under conditions disrupting tetraspan interactions. , 1999, The Biochemical journal.
[46] D. Azorsa,et al. Selective tetraspan–integrin complexes (CD81/α4β1, CD151/α3β1, CD151/α6β1) under conditions disrupting tetraspan interactions , 1999 .
[47] M. Houghton,et al. Binding of hepatitis C virus to CD81. , 1998, Science.
[48] R. Yauch,et al. Highly stoichiometric, stable, and specific association of integrin alpha3beta1 with CD151 provides a major link to phosphatidylinositol 4-kinase, and may regulate cell migration. , 1998, Molecular biology of the cell.
[49] S. Mayor,et al. GPI-anchored proteins are organized in submicron domains at the cell surface , 1998, Nature.
[50] T. Kurzchalia,et al. Microdomains of GPI-anchored proteins in living cells revealed by crosslinking , 1998, Nature.
[51] K. Simons,et al. Cholesterol Is Required for Surface Transport of Influenza Virus Hemagglutinin , 1998, The Journal of cell biology.
[52] M C Phillips,et al. Use of cyclodextrins for manipulating cellular cholesterol content. , 1997, Journal of lipid research.
[53] E. Ikonen,et al. Functional rafts in cell membranes , 1997, Nature.
[54] S. Levy,et al. Normal Lymphocyte Development but Delayed Humoral Immune Response in CD81-null Mice , 1997, The Journal of experimental medicine.
[55] J. N. Flynn,et al. FIV infection of the domestic cat: an animal model for AIDS. , 1997, Immunology today.
[56] V. ter meulen,et al. CD9, a tetraspan transmembrane protein, renders cells susceptible to canine distemper virus , 1997, Journal of virology.
[57] C. Boucheix,et al. CD9, CD63, CD81, and CD82 are components of a surface tetraspan network connected to HLA‐DR and VLA integrins , 1996, European journal of immunology.
[58] W. J. Johnson,et al. Cellular Cholesterol Efflux Mediated by Cyclodextrins , 1996, The Journal of Biological Chemistry.
[59] M. Zutter,et al. Characterization of novel complexes on the cell surface between integrins and proteins with 4 transmembrane domains (TM4 proteins). , 1996, Molecular biology of the cell.
[60] W. J. Johnson,et al. Cellular Cholesterol Efflux Mediated by Cyclodextrins (*) , 1995, The Journal of Biological Chemistry.
[61] C. Boucheix,et al. CD9 antigen is an accessory subunit of the VLA integrin complexes , 1994, European journal of immunology.
[62] T. Mitamura,et al. Heparin‐binding EGF‐like growth factor, which acts as the diphtheria toxin receptor, forms a complex with membrane protein DRAP27/CD9, which up‐regulates functional receptors and diphtheria toxin sensitivity. , 1994, The EMBO journal.
[63] L. Rénia,et al. A malaria heat‐shock‐like determinant expressed on the infected hepatocyte surface is the target of antibody‐dependent cell‐mediated cytotoxic mechanisms by nonparenchymal liver cells , 1990, European journal of immunology.
[64] M. Hollingdale,et al. In vitro cultivation of the exoerythrocytic stage of Plasmodium berghei in a hepatoma cell line. , 1983, The American journal of tropical medicine and hygiene.
[65] Y. Wada,et al. Potentiation of the ligand-binding activity of integrin alpha3beta1 via association with tetraspanin CD151. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[66] S. Levy,et al. Hepatocyte CD81 is required for Plasmodium falciparum and Plasmodium yoelii sporozoite infectivity , 2003, Nature Medicine.
[67] E. Odintsova,et al. Expression of the palmitoylation-deficient CD151 weakens the association of alpha 3 beta 1 integrin with the tetraspanin-enriched microdomains and affects integrin-dependent signaling. , 2002, The Journal of biological chemistry.
[68] A. Joyner,et al. Production of targeted embryonic stem cell clones. , 1993 .
[69] Alexandra L. Joyner,et al. Gene targeting: a practical approach. , 1993 .