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NCAM‐derived peptides function as agonists for the fibroblast growth factor receptor
Author(s) -
Hansen Stine M. M.,
Køhler Lene B.,
Li Shizhong,
Kiselyov Vladislav,
Christensen Claus,
Owczarek Sylwia,
Bock Elisabeth,
Berezin Vladimir
Publication year - 2008
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.2008.05544.x
Subject(s) - fibroblast growth factor receptor , neural cell adhesion molecule , neurite , receptor , microbiology and biotechnology , fibroblast growth factor , function (biology) , biology , chemistry , biochemistry , cell adhesion , cell , in vitro
The neural cell adhesion molecule (NCAM) directly interacts with the fibroblast growth factor receptor (FGFR). Both fibronectin type III (FN3) modules of NCAM are involved in this interaction. One of the NCAM–FGFR contact sites has been localized recently to the upper N‐terminal part of the second NCAM FN3 module encompassing the F and G β‐strands and the interconnecting loop region. Here, we investigated whether any of the six putative strand‐loop‐strand regions in the first NCAM FN3 module are involved in FGFR interactions. Peptide sequences encompassing these regions, termed encamins, were synthesized and tested for their ability to bind and activate FGFR. Encamins localized to the N‐terminal part of the first FN3 module did not interact with FGFR, whereas encamins localized to the C‐terminal part, termed EncaminA, C and E, bound to and activated FGFR. The encamins induced FGFR‐dependent neurite outgrowth, and EncaminC and E promoted neuronal survival and enhanced pre‐synaptic function. In conclusion, the interaction between NCAM and FGFR probably involves multiple contact sites at an interface formed by the two NCAM FN3 modules and FGFR, and encamins could constitute important pharmacological tools for the study of specific functional aspects of NCAM, including neuroprotection and modulation of plasticity.