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Sökning: onr:"swepub:oai:DiVA.org:uu-193349" > Interplay between α...

Interplay between αvβ3 Integrin and Nucleolin Regulates Human Endothelial and Glioma Cell Migration

Koutsioumpa, Marina (författare)
Department of Pharmacy, Laboratory of Molecular Pharmacology, University of Patras, Greece
Polytarchou, Christos (författare)
Department of Cancer Immunology & AIDS, Dana Farber Cancer Institute, Boston, Massachusetts 02215, USA
Courty, José (författare)
Laboratoire CRRET, Universite Paris Est Creteil Val de Marne, avenue du General de Gaulle, 94010 Creteil Cedex, France
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Zhang, Yue (författare)
Sino-French Research Centre for Life Sciences and Genomics, CNRS/LIA124, Rui Jin Hospital, Jiao Tong University Medical School, 197 Rui Jin Er Road, Shanghai 200025, China
Kieffer, Nelly (författare)
Sino-French Research Centre for Life Sciences and Genomics, CNRS/LIA124, Rui Jin Hospital, Jiao Tong University Medical School, 197 Rui Jin Er Road, Shanghai 200025, China
Mikelis, Constantinos (författare)
Department of Pharmacy, Laboratory of Molecular Pharmacology, University of Patras, Greece
Skandalis, Spyros S (författare)
Uppsala universitet,Ludwiginstitutet för cancerforskning
Hellman, Ulf (författare)
Uppsala universitet,Ludwiginstitutet för cancerforskning
Iliopoulos, Dimitrios (författare)
Department of Cancer Immunology & AIDS, Dana Farber Cancer Institute, Boston, Massachusetts 02215, USA
Papadimitriou, Evangelia (författare)
Department of Pharmacy, Laboratory of Molecular Pharmacology, University of Patras, Greece
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 (creator_code:org_t)
2013
2013
Engelska.
Ingår i: Journal of Biological Chemistry. - 0021-9258 .- 1083-351X. ; 288:1, s. 343-354
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • The multifunctional protein nucleolin (NCL) is overexpressed on the surface of activated endothelial and tumor cells and mediates the stimulatory actions of several angiogenic growth factors, such as pleiotrophin (PTN). Because α(v)β(3) integrin is also required for PTN-induced cell migration, the aim of the present work was to study the interplay between NCL and α(v)β(3) by using biochemical, immunofluorescence, and proximity ligation assays in cells with genetically altered expression of the studied molecules. Interestingly, cell surface NCL localization was detected only in cells expressing α(v)β(3) and depended on the phosphorylation of β(3) at Tyr(773) through receptor protein-tyrosine phosphatase β/ζ (RPTPβ/ζ) and c-Src activation. Downstream of α(v)β(3,) PI3K activity mediated this phenomenon and cell surface NCL was found to interact with both α(v)β(3) and RPTPβ/ζ. Positive correlation of cell surface NCL and α(v)β(3) expression was also observed in human glioblastoma tissue arrays, and inhibition of cell migration by cell surface NCL antagonists was observed only in cells expressing α(v)β(3). Collectively, these data suggest that both expression and β(3) integrin phosphorylation at Tyr(773) determine the cell surface localization of NCL downstream of the RPTPβ/ζ/c-Src signaling cascade and can be used as a biomarker for the use of cell surface NCL antagonists as anticancer agents.

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