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First published online 27 November 2007
doi: 10.1242/jcs.010744

Journal of Cell Science 120, 4388-4394 (2007)
Published by The Company of Biologists 2007
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Research Article

Neural cell adhesion molecule regulates the cellular response to fibroblast growth factor

Chiara Francavilla1, Sébastien Loeffler1,*, Daniele Piccini1, Angelika Kren2, Gerhard Christofori2 and Ugo Cavallaro1,{ddagger}

1 IFOM-FIRC Institute of Molecular Oncology, I-20139 Milano, Italy
2 Institute of Biochemistry and Genetics, Department of Clinical-Biological Sciences, Center of Biomedicine, University of Basel, Switzerland

{ddagger} Author for correspondence (e-mail: ugo.cavallaro{at}ifom-ieo-campus.it)

Accepted 14 October 2007

Neural cell adhesion molecule (NCAM) mediates cell-cell adhesion and signaling in the nervous system, yet NCAM is also expressed in non-neural tissues, in which its function has in most parts remained elusive. We have previously reported that NCAM stimulates cell-matrix adhesion and neurite outgrowth by activating fibroblast growth factor receptor (FGFR) signaling. Here, we investigated whether the interplay between NCAM and FGFR has any impact on the response of FGFR to its classical ligands, FGFs. To this end, we employed two fibroblast cell lines, NCAM-negative L cells and NCAM-positive NIH-3T3 cells, in which the expression of NCAM was manipulated by means of transfection or RNAi technologies, respectively. The results demonstrate that NCAM expression reduces FGF-stimulated ERK1/2 activation, cell proliferation and cell-matrix adhesion, in both L and NIH-3T3 cells. Furthermore, our data show that NCAM inhibits the binding of FGF to its high-affinity receptor in a competitive manner, providing the mechanisms for the NCAM-mediated suppression of FGF function. In this context, a small peptide that mimics the binding of NCAM to FGFR was sufficient to block FGF-dependent cell proliferation. These findings point to NCAM as being a major regulator of FGF-FGFR interaction, thus introducing a novel type of control mechanism for FGFR activity and opening new therapeutic perspectives for those diseases characterized by aberrant FGFR function.

Key words: Neural cell adhesion molecule, Fibroblast growth factor receptor, Signaling, Receptor binding




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