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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.
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