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Complex Formation of a Brain-Derived Neurotrophic Factor and Glycosaminoglycans
Author(s) -
Yukihiro Kanato,
Sayaka Ono,
Ken Kitajima,
Chihiro Sato
Publication year - 2009
Publication title -
bioscience biotechnology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.509
H-Index - 116
eISSN - 1347-6947
pISSN - 0916-8451
DOI - 10.1271/bbb.90637
Subject(s) - neurotrophin , tropomyosin receptor kinase b , neurotrophic factors , brain derived neurotrophic factor , microbiology and biotechnology , trk receptor , polysialic acid , chemistry , extracellular matrix , glycosaminoglycan , receptor , biochemistry , biology , cell , cell adhesion , neural cell adhesion molecule
Glycosaminoglycans (GAGs), large anionic glycopolymers, are the glycan portion of proteoglycans and are important components of the extracellular matrix. Recently we reported that polysialic acid, a polyanionic glycopolymer specific to the brain, binds neurotrophic factors to form a large complex. It is not clear whether GAGs also bind neurotrophic factors to form a large complex. In the present study, we demonstrate that a brain-derived neurotrophic factor (BDNF) dimer directly binds GAGs other than chondroitin and hyaluronic acid to form a large complex. Neurotrophin-3 showed similar GAG binding properties. Furthermore, BDNF, after forming a large complex with GAG, bound to the BDNF receptors tropomyosin-related kinase (Trk) B and p75 neurotrophin receptor (NTR). These findings suggest that GAGs function to produce a reservoir of BDNF and other neurotrophic factors, and may serve to regulate their local concentrations on the cell surface.

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