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HIV-Tat dependent chemotaxis and invasion, key aspects of Tat mediated pathogenesis

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Abstract

Extracellular Tat acts as a pleiotropic molecule inducing several biological effects on different target cells. Tat stimulates the chemotaxis of numerous cell types and it appears to have oncogenic activities, including acting as a co-factor for Kaposi's sarcoma. The Tat protein has been shown to bind integrins through an RGD amino acid motif. Tat is an angiogenic factor able to induce the migration and invasion of endothelial and KS cells through the interaction of its basic domain with the VEGF receptor VEGFR2 (Flk-1/KDR). We have also found that Tat is able to mimic chemokines, activating monocyte migration through the `chemokine like' cysteine-core domain. Tat is a chemoattractant for dendritic cells, and both the RGD and basic domains appear to be involved in this response. In a recent study we demonstrated that Tat is chemotactic for PMN and induces Ca2+ mobilization in vitro. Experiments using synthetic peptides showed that Tat activities on PMN are mediated by the `chemokine like' region. Finally Tat is also able to induce B cell chemotaxis, while its activity on helper T cells has not yet been clarified. Here we review data on Tat-dependent chemotaxis and discuss the possible implications in Tat mediated pathogenesis.

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References

  1. Gatignol A, Jeang K-T. Tat as a transcriptional activator and a potential therapeutic target for HIV-1. In Jean K-T (ed): HIV-1: Molecular Biology and Pathogenesis. San Diego, California: Academic Press 2000; 209–27

    Google Scholar 

  2. Lotz M, Clark LI, Ganu V. HIV-1 transactivator protein Tat induces proliferation and TGF beta expression in human articular chondrocytes. J Cell Biol 1994; 124(3): 365–71.

    Article  PubMed  CAS  Google Scholar 

  3. Westendorp MO et al. Human immunodeficiency virus type 1 Tat upregulates interleukin-2 secretion in activated T cells. J Virol 1994; 68(7): 4177–85.

    PubMed  CAS  Google Scholar 

  4. Scala G et al. The expression of the interleukin 6 gene is induced by the human immunodeficiency virus 1 TAT protein. J Exp Med 1994; 179(3): 961–71.

    Article  PubMed  CAS  Google Scholar 

  5. Buonaguro L et al. Effects of the human immunodeficiency virus type 1 Tat protein on the expression of inflammatory cytokines. J Virol 1992; 66(12): 7159–67.

    PubMed  CAS  Google Scholar 

  6. Buonaguro L et al. The human immunodeficiency virus type 1 Tat protein transactivates tumor necrosis factor beta gene expression through a TAR-like structure. J Virol 1994; 68(4): 2677–82.

    PubMed  CAS  Google Scholar 

  7. Sastry K et al. HIV-1 tat gene induces tumor necrosis factor-beta (lymphotoxin) in a human B-lymphoblastoid cell line. J Biol Chem 1990; 265: 20091–3.

    PubMed  CAS  Google Scholar 

  8. Howcroft TK et al Repression of MHC class I gene promoter activity by two-exon Tat of HIV. Science1993; 260(5112): 1320–2.

    PubMed  CAS  Google Scholar 

  9. Taylor J et al. Activation of expression of genes coding for extracellular matrix protein in Tat-producing glioblastoma cells. Proc Natl Acad Sci USA 1992; 89: 9617–21.

    Article  PubMed  CAS  Google Scholar 

  10. Longo F et al. A novel approach to protein-protein interaction: complex formation between the p53 tumor suppressor and the HIV Tat proteins. Biochem Biophys Res Commun 1995; 206(1): 326–34.

    Article  PubMed  CAS  Google Scholar 

  11. Garcia JA et al. Functional domains required for tat-induced transcriptional activation of the HIV-1 long terminal repeat. EMBO J 1988; 7: 3143–7.

    PubMed  CAS  Google Scholar 

  12. Brake D, Debouck C, Biesecker G. Identification of an Arg-Gly-Asp (RGD) cell adhesion site in human immunodeficiency virus type 1 transactivation protein, tat. J Cell Biol 1990; 111: 1275–81.

    Article  PubMed  CAS  Google Scholar 

  13. Ensoli B et al. Release, uptake, and effects of extracellular human immunodeficiency virus type 1 Tat protein on cell growth and viral transactivation. J Virol 1993; 67(1): 277–87.

    PubMed  CAS  Google Scholar 

  14. Frankel AD, Pabo CO. Cellular uptake of the tat protein from human immunodeficiency virus. Cell 1988; 55: 1189–93.

    Article  PubMed  CAS  Google Scholar 

  15. Barillari G et al. The Tat protein of human immunodeficiency virus type 1, a growth factor for AIDS Kaposi sarcoma and cytokineactivated vascular cells, induces adhesion of the same cell types by using integrin receptors recognizing the RGD amino acid sequence. Proc Natl Acad Sci USA 1993; 90(17): 7941–5.

    Article  PubMed  CAS  Google Scholar 

  16. Mitola S et al. Tat-human immunodeficiency virus-1 induces human monocyte chemotaxis by activation of vascular endothelial growth factor receptor-1. Blood 1997; 90: 1365–72.

    PubMed  CAS  Google Scholar 

  17. Albini A et al. The angiogenesis induced by HIV-1 Tat is mediated by the flk-1/KDR receptor on vascular endothelial cells. Nat Med 1996; 2(12): 1371–5.

    Article  PubMed  CAS  Google Scholar 

  18. Albini A et al. HIV-1 Tat protein mimicry of chemokines. Proc Natl Acad Sci USA 1998; 95(22): 13153–8.

    Article  PubMed  CAS  Google Scholar 

  19. Ghezzi S et al. Inhibition of CXCR4-dependent HIV-1 infection by extracellular HIV-1 Tat. Biochem Biophys Res Commun 2000; 270(3): 992–6.

    Article  PubMed  CAS  Google Scholar 

  20. Gutheil WG et al. Human immunodeficiency virus 1 Tat binds to dipeptidyl aminopeptidase IV (CD26): A possible mechanism for Tat's immunosuppressive activity. Proc Natl Acad Sci USA 1994; 91(14): 6594–8.

    Article  PubMed  CAS  Google Scholar 

  21. Noonan DM, Albini A. From the outside in: extracellular activities of HIV Tat. In Jeang K-T (ed): HIV-1: Molecular Biology and Pathogenesis. San Diego, California: Academic Press 2000; 229–50.

    Google Scholar 

  22. Kim CM et al. The HIV tat gene transforms human keratinocytes. Oncogene 1992; 7(8): 1525–9.

    PubMed  CAS  Google Scholar 

  23. Corallini A et al. Systemic expression of HIV1 tat gene in transgenic mice induces endothelial proliferation and tumors of different histotypes. Cancer Res 1993; 53: 5569–75.

    PubMed  CAS  Google Scholar 

  24. Corallini A et al. Promotion of tumor metastases and induction of angiogenesis by native HIV-1 Tat protein from BK virus/tat transgenic mice. AIDS 1996; 10: 701–10.

    PubMed  CAS  Google Scholar 

  25. Kundu RK et al. Expression of the human immunodeficiency virus-Tat gene in lymphoid tissues of transgenic mice is associated with B-cell lymphoma. Blood 1999; 94(1): 275–82.

    PubMed  CAS  Google Scholar 

  26. Albini A et al. Angiogenic potential in vivo by Kaposi sarcoma cellfree supernatants and HIV1-tat product: Inhibition of KS-like lesions by TIMP-2. AIDS 1994; 8: 1237–44.

    Article  PubMed  CAS  Google Scholar 

  27. Albini A et al. Angiogenic properties of human immunodeficiency virus type 1 Tat protein. Proc Natl Acad Sci USA 1995; 92: 4838–42.

    Article  PubMed  CAS  Google Scholar 

  28. Ensoli B et al. Synergy between basic fibroblast growth factor and HIV-1 tat protein in induction of Kaposi's sarcoma. Nature 1994; 371: 674–80.

    Article  PubMed  CAS  Google Scholar 

  29. Albini A et al. HIV-tat protein is a heparin-binding angiogenic growth factor. Oncogene 1996; 12: 289–97.

    PubMed  CAS  Google Scholar 

  30. Ganju RK et al. Human immunodeficiency virus tat modulates the Flk-1/KDR receptor, mitogen-activated protein kinases, and components of focal adhesion in Kaposi's sarcoma cells. J Virol 1998; 72(7): 6131–7.

    PubMed  CAS  Google Scholar 

  31. Montaldo F et al. Expression of functional tyrosine kinases on immortalized Kaposi's sarcoma cells. J Cell Physiol 2000; 184(2): 246–54.

    Article  PubMed  CAS  Google Scholar 

  32. Morini M et al. Kaposi's Sarcoma Cells of Different Etiologic Origins Respond to HIV-Tat through the Flk-1/KDR (VEGFR-2): Relevance in AIDS-KS Pathology. Biochem Biophys Res Commun 2000; 273(1): 267–71.

    Article  PubMed  CAS  Google Scholar 

  33. Arese M et al. HIV-1 Tat protein stimulates in vivo vascular permeability and lymphomononuclear cell recruitment. J Immunol 2001; 166(2): 1380–8.

    PubMed  CAS  Google Scholar 

  34. Falcioni R et al. Alpha 6 beta 4 and alpha 6 beta 1 integrins associate with erbB-2 in human carcinoma cell lines. Exp Cell Res 1997; 236(1): 76–85.

    Article  PubMed  CAS  Google Scholar 

  35. Soldi R et al. Role of αvβ3 integrin in the activation of vascular endothelial growth factor receptor-2. Embo J 1999; 18(4): 882–92.

    Article  PubMed  CAS  Google Scholar 

  36. Barillari G et al. The Tat protein of human immunodeficiency virus type-1 promotes vascular cell growth and locomotion by engaging the α5β1 and αvβ3 integrins and by mobilizing sequestered basic fibroblast growth factor. Blood 1999; 94(2): 663–72.

    PubMed  CAS  Google Scholar 

  37. Biancone L et al. Motility induced by human immunodeficiency virus-1 tat on Kaposi's sarcoma cells requires platelet-activating factor synthesis. Am J Pathol 1999; 155(5): 1731–9.

    PubMed  CAS  Google Scholar 

  38. Del Sorbo L et al. Tat-induced platelet-activating factor synthesis contributes to the angiogenic effect of HIV-1 Tat. Eur J Immunol 2001;: 31(2): 376–83.

    Article  PubMed  CAS  Google Scholar 

  39. Benelli R et al. Monocyte-derived dendritic cells and monocytes migrate to HIV-Tat RGD and basic peptides. AIDS 1998; 12: 261–8.

    Article  PubMed  CAS  Google Scholar 

  40. Zocchi MR, Poggi A, Rubartelli A. The RGD-containing domain of exogenous HIV-1 Tat inhibits the engulfment of apoptotic bodies by Dendritic cells. AIDS 1997; 11: 1227–35.

    Article  PubMed  CAS  Google Scholar 

  41. Lafrenie RM et al. HIV-1-Tat modulates the function of monocytes and alters their interactions with microvessel endothelial cells. A mechanism of HIV pathogenesis. J Immunol 1996; 156(4): 1638–45.

    PubMed  CAS  Google Scholar 

  42. Lafrenie RM et al. HIV-1-Tat protein promotes chemotaxis and invasive behavior by monocytes. J Immunol 1996; 157(3): 974–7.

    PubMed  CAS  Google Scholar 

  43. Albini A et al. Identification of a novel domain of HIV Tat involved in monocyte chemotaxis. J Biol Chem 1998; 273: 15895–900.

    Article  PubMed  CAS  Google Scholar 

  44. Brodie SJ et al. HIV-specific cytotoxic T lymphocytes traffic to lymph nodes and localize at sites of HIV replication and cell death. J Clin Invest 2000; 105(10): 1407–17.

    Article  PubMed  CAS  Google Scholar 

  45. Roulston A et al. Regulation of human immunodeficiency virus type 1 and cytokine gene expression in myeloid cells by NF-kappa B/Rel transcription factors. Microbiol Rev 1995; 59(3): 481–505.

    PubMed  CAS  Google Scholar 

  46. Park IW, Wang JF, Groopman JE. HIV-1 Tat promotes monocyte chemoattractant protein-1 secretion followed by transmigration of monocytes. Blood 2001; 97(2): 352–8.

    Article  PubMed  CAS  Google Scholar 

  47. Kutsch O et al. Induction of the chemokines interleukin-8 and IP-10 by human immunodeficiency virus type 1 tat in astrocytes. J Virol 2000; 74(19): 9214–21.

    Article  PubMed  CAS  Google Scholar 

  48. Del Sorbo L et al. The synthesis of platelet-activating factor modulates chemotaxis of monocytes induced by HIV-1 Tat. Eur J Immunol 1999; 29(5): 1513–21.

    Article  PubMed  CAS  Google Scholar 

  49. Xiao H et al. Selective CXCR4 antagonism by tat: implications for in vivo expansion of coreceptor use by HIV-1. Proc Natl Acad Sci USA 2000; 97(21): 11466–71.

    Article  PubMed  CAS  Google Scholar 

  50. Benelli R et al. Human immunodeficiency virus transactivator protein (Tat) stimulates chemotaxis, calcium mobilization, and activation of human polymorphonuclear leukocytes: Implications for Tat-mediated pathogenesis. J Infect Dis 2000; 182(6): 1643–51.

    Article  PubMed  CAS  Google Scholar 

  51. Prakash O et al. The human immunodeficiency virus type I Tat protein potentiates ethanol-induced neutrophil functional impairment in transgenic mice. Alcohol Clin Exp Res 1998; 22(9): 2043–9.

    PubMed  CAS  Google Scholar 

  52. de Paulis A et al. Tat protein is an HIV-1-encoded α-chemokine homolog that promotes migration and up-regulates CCR3 expression on human FcεRI(+) cells. J Immunol 2000; 165(12): 7171–9.

    PubMed  CAS  Google Scholar 

  53. Rappaport J et al. Molecular pathway involved in HIV-1-induced CNS pathology: Role of viral regulatory protein, Tat. J Leuk Biol 1999; 65(4): 458–65.

    CAS  Google Scholar 

  54. Philippon V et al. The basic domain of the lentiviral Tat protein is responsible for damages in mouse brain: Involvement of cytokines. Virology 1994; 205(2): 519–29.

    Article  PubMed  CAS  Google Scholar 

  55. Hegg CC et al. Beta-chemokines and human immunodeficiency virus type-1 proteins evoke intracellular calcium increases in human microglia. Neuroscience 2000; 98(1): 191–9.

    Article  PubMed  CAS  Google Scholar 

  56. Vogel J et al. The HIV tat gene induces dermal lesions resembling Kaposi's sarcoma in transgenic mice. Nature 1988; 335(13): 606–11.

    Article  PubMed  CAS  Google Scholar 

  57. Chirivi RG et al. Human immunodeficiency virus-1 (HIV-1)-Tat protein promotes migration of acquired immunodeficiency syndromerelated lymphoma cells and enhances their adhesion to endothelial cells. Blood 1999; 94(5): 1747–54.

    PubMed  CAS  Google Scholar 

  58. Shutt DC, Soll DR. HIV-induced T-cell syncytia release a two component T-helper cell chemoattractant composed of Nef and Tat. J Cell Sci 1999; 112(Pt 22): 3931–41.

    PubMed  CAS  Google Scholar 

  59. Fiorelli V et al. IFN-gamma induces endothelial cells to proliferate and to invade the extracellular matrix in response to the HIV-1 Tat protein: Implications for AIDS-Kaposi's sarcoma pathogenesis. J Immunol 1999. 162(2): 1165–70.

    PubMed  CAS  Google Scholar 

  60. Prakash O et al. Human Kaposi's sarcoma cell-mediated tumorigenesis in human immunodeficiency type 1 tat-expressing transgenic mice. J Natl Cancer Inst 2000; 92(9): 721–8.

    Article  PubMed  CAS  Google Scholar 

  61. Kumar A et al. Human immunodeficiency virus-1-tat induces matrix metalloproteinase-9 in monocytes through protein tyrosine phosphatase-mediated activation of nuclear transcription factor NFkappaB. FEBS Lett 1999; 462(1-2): 140–4.

    Article  PubMed  CAS  Google Scholar 

  62. Johnston JB et al. HIV-1 Tat neurotoxicity is prevented by matrix metalloproteinase inhibitors. Ann Neurol 2001; 49(2): 230–41.

    Article  PubMed  CAS  Google Scholar 

  63. Bayer P et al. Structural studies of HIV-1 Tat protein. J Mol Biol 1995; 247(4): 529–35.

    Article  PubMed  CAS  Google Scholar 

  64. Rubartelli A, Sitia R. Secretion of mammalian proteins that lack a signal sequence. In Kuchler K, Rubartelli A and Holland B (eds): Unusual Secretory Pathways: From Bacteria to Man. Heidelberg: Springer-Verlag 1997; 87–114.

    Google Scholar 

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Vené, R., Benelli, R., Noonan, D. et al. HIV-Tat dependent chemotaxis and invasion, key aspects of Tat mediated pathogenesis. Clin Exp Metastasis 18, 533–538 (2000). https://doi.org/10.1023/A:1011991906685

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