This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Mitola, S.
Right arrow Articles by Bussolino, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Mitola, S.
Right arrow Articles by Bussolino, F.

 Previous Article  |  Next Article 

Journal of Virology, January 2000, p. 344-353, Vol. 74, No. 1
0022-538X/0/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.

Identification of Specific Molecular Structures of Human Immunodeficiency Virus Type 1 Tat Relevant for Its Biological Effects on Vascular Endothelial Cells

Stefania Mitola,1,2 Raffaella Soldi,1,2 Ilaria Zanon,1,2 Luca Barra,1,2 Maria Ines Gutierrez,3 Ben Berkhout,4 Mauro Giacca,3 and Federico Bussolino1,2,*

Institute for Cancer Research and Treatment (I.R.C.C.), 10060 Candiolo,1 Department of Genetics, Biology and Biochemistry, School of Medicine, University of Torino, 10100 Turin,2 and Molecular Medicine Laboratory, International Centre for Genetic Engineering and Biotechnology, 34102 Trieste,3 Italy, and Department of Human Retrovirology, University of Amsterdam, Academic Medical Center, 1100 DE Amsterdam, The Netherlands4

Received 28 May 1999/Accepted 17 September 1999

Human immunodeficiency virus type 1 (HIV-1) Tat transactivates viral genes and is released by infected cells, acting as a soluble mediator. In endothelial cells (EC), it activates a proangiogenic program by activating vascular endothelial growth factor receptor type 2 (VEGFR-2) and integrins. A structure-activity relationship study was performed by functional analysis of Tat substitution and deletion variants to define the Tat determinants necessary for EC activation. Variants were made (i) in the basic and (ii) in the cysteine-rich domains and (iii) in the C-terminal region containing the RGD sequence required for integrin recognition. Our results led to the following conclusions. (i) Besides a high-affinity binding site corresponding to VEGFR-2, EC express low-affinity binding sites. (ii) The basic and the cysteine-rich variants bind only to the low-affinity binding sites and do not promote tyrosine phosphorylation of VEGFR-2. Furthermore, they have a reduced ability to activate EC in vitro, and they lack angiogenic activity. (iii) Mutants with mutations in the C-terminal region are partially defective for in vitro biological activities and in vivo angiogenesis, but they activate VEGFR-2 as Tat wild type. In conclusion, regions encoded by the first exon of tat are necessary and sufficient for activation of VEGFR-2. However, the C-terminal region, most probably through RGD-mediated integrin engagement, is indispensable for full activation of an in vitro and in vivo angiogenic program.


* Corresponding author. Mailing address: I.R.C.C., Strada Provinciale 142, Km 3.95, 10060 Candiolo (Turin), Italy. Phone: 39-011-9933347. Fax: 39-011-9933524. E-mail: fbussoli{at}mail.ircc.unito.it.


Journal of Virology, January 2000, p. 344-353, Vol. 74, No. 1
0022-538X/0/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Wu, R. F., Ma, Z., Myers, D. P., Terada, L. S. (2007). HIV-1 Tat Activates Dual Nox Pathways Leading to Independent Activation of ERK and JNK MAP Kinases. J. Biol. Chem. 282: 37412-37419 [Abstract] [Full Text]  
  • Bugatti, A., Urbinati, C., Ravelli, C., De Clercq, E., Liekens, S., Rusnati, M. (2007). Heparin-Mimicking Sulfonic Acid Polymers as Multitarget Inhibitors of Human Immunodeficiency Virus Type 1 Tat and gp120 Proteins. Antimicrob. Agents Chemother. 51: 2337-2345 [Abstract] [Full Text]  
  • Toschi, E., Bacigalupo, I., Strippoli, R., Chiozzini, C., Cereseto, A., Falchi, M., Nappi, F., Sgadari, C., Barillari, G., Mainiero, F., Ensoli, B. (2006). HIV-1 Tat Regulates Endothelial Cell Cycle Progression via Activation of the Ras/ERK MAPK Signaling Pathway. Mol. Biol. Cell 17: 1985-1994 [Abstract] [Full Text]  
  • Kittiworakarn, J., Lecoq, A., Moine, G., Thai, R., Lajeunesse, E., Drevet, P., Vidaud, C., Menez, A., Leonetti, M. (2006). HIV-1 Tat Raises an Adjuvant-free Humoral Immune Response Controlled by Its Core Region and Its Ability to Form Cysteine-mediated Oligomers. J. Biol. Chem. 281: 3105-3115 [Abstract] [Full Text]  
  • Urbinati, C., Mitola, S., Tanghetti, E., Kumar, C., Waltenberger, J., Ribatti, D., Presta, M., Rusnati, M. (2005). Integrin {alpha}V{beta}3 as a Target for Blocking HIV-1 Tat-Induced Endothelial Cell Activation In Vitro and Angiogenesis In Vivo. Arterioscler. Thromb. Vasc. Bio. 25: 2315-2320 [Abstract] [Full Text]  
  • Urbinati, C., Bugatti, A., Giacca, M., Schlaepfer, D., Presta, M., Rusnati, M. (2005). {alpha}v{beta}3-integrin-dependent activation of focal adhesion kinase mediates NF-{kappa}B activation and motogenic activity by HIV-1 Tat in endothelial cells. J. Cell Sci. 118: 3949-3958 [Abstract] [Full Text]  
  • Marchio, S., Alfano, M., Primo, L., Gramaglia, D., Butini, L., Gennero, L., De Vivo, E., Arap, W., Giacca, M., Pasqualini, R., Bussolino, F. (2005). Cell surface-associated Tat modulates HIV-1 infection and spreading through a specific interaction with gp120 viral envelope protein. Blood 105: 2802-2811 [Abstract] [Full Text]  
  • Wu, R. F., Gu, Y., Xu, Y. C., Mitola, S., Bussolino, F., Terada, L. S. (2004). Human Immunodeficiency Virus Type 1 Tat Regulates Endothelial Cell Actin Cytoskeletal Dynamics through PAK1 Activation and Oxidant Production. J. Virol. 78: 779-789 [Abstract] [Full Text]  
  • Ahmed, S, Siddiqui, R K, Siddiqui, A K, Zaidi, S A, Cervia, J (2002). HIV associated thrombotic microangiopathy. Postgrad. Med. J. 78: 520-524 [Abstract] [Full Text]  
  • Barillari, G., Ensoli, B. (2002). Angiogenic Effects of Extracellular Human Immunodeficiency Virus Type 1 Tat Protein and Its Role in the Pathogenesis of AIDS-Associated Kaposi's Sarcoma. Clin. Microbiol. Rev. 15: 310-326 [Abstract] [Full Text]  
  • Arese, M., Ferrandi, C., Primo, L., Camussi, G., Bussolino, F. (2001). HIV-1 Tat Protein Stimulates In Vivo Vascular Permeability and Lymphomononuclear Cell Recruitment. J. Immunol. 166: 1380-1388 [Abstract] [Full Text]  
  • Battaglia, P. A., Zito, S., Macchini, A., Gigliani, F. (2001). A Drosophila model of HIV-Tat-related pathogenicity. J. Cell Sci. 114: 2787-2794 [Abstract] [Full Text]