Protective effects of polysialic acid on proteolytic cleavage of FGF2 and proBDNF/BDNF

被引:33
作者
Hane, Masaya [1 ,2 ]
Matsuoka, Shuhei [1 ,2 ]
Ono, Sayaka [1 ]
Miyata, Shinji [1 ]
Kitajima, Ken [1 ]
Sato, Chihiro [1 ]
机构
[1] Nagoya Univ, Biosci & Biotechnol Ctr, Nagoya, Aichi 4648601, Japan
[2] Nagoya Univ, Sch Bioagr Sci, Nagoya, Aichi 4648601, Japan
关键词
BDNF; FGF2; NCAM; plasmin; polysialic acid; polysialyltransferase; proBDNF; SPR; ST8SIA2/STX; Trypsin; CELL-ADHESION MOLECULE; FIBROBLAST-GROWTH-FACTOR; NEUROTROPHIC FACTOR; MUTATED POLYSIALYLTRANSFERASE; FUNCTIONAL IMPAIRMENTS; MAMMALIAN BRAIN; SCHIZOPHRENIA; EXPRESSION; PLASTICITY; MICE;
D O I
10.1093/glycob/cwv049
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Polysialic acid (polySia) is a linear polymer of sialic acid that modifies neural cell adhesion molecule (NCAM) in the vertebrate brain. PolySia is a large and exclusive molecule that functions as a negative regulator of cell-cell interactions. Recently, we demonstrated that polySia can specifically bind fibroblast growth factor 2 (FGF2) and BDNF; however, the protective effects of polySia on the proteolytic cleavage of these proteins remain unknown, although heparin/heparan sulfate has been shown to impair the cleavage of FGF2 by trypsin. Here, we analyzed the protective effects of polySia on the proteolytic cleavage of FGF2 and proBDNF/BDNF. We found that polySia protected intact FGF2 from tryptic activity via the specific binding of extended polySia chains on NCAM to FGF2. Oligo/polySia also functioned to impair the processing of proBDNF by plasmin via binding of oligo/polySia chains on NCAM. In addition, the polySia structure synthesized by mutated polysialyltransferase, ST8SIA2/STX(SNP7), which was previously identified from a schizophrenia patient, was impaired for these functions compared with polySia produced by normal ST8SIA2. Taken together, these data suggest that the protective effects of polySia toward FGF2 and proBDNF may be involved in the regulation of the concentrations of these neurologically active molecules.
引用
收藏
页码:1112 / 1124
页数:13
相关论文
共 51 条
[1]   Sialyltransferase ST8Sia-II assembles a subset of polysialic acid that directs hippocampal axonal targeting and promotes fear behavior [J].
Angata, K ;
Long, JM ;
Bukalo, O ;
Lee, W ;
Dityatev, A ;
Wynshaw-Boris, A ;
Schachner, M ;
Fukuda, M ;
Marth, JD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (31) :32603-32613
[2]   Molecular dissection of the ST8Sia IV polysialyltransferase - Distinct domains are required for neural cell adhesion molecule recognition and polysialylation [J].
Angata, K ;
Chan, D ;
Thibault, J ;
Fukuda, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (24) :25883-25890
[3]   A genome-wide scan for common alleles affecting risk for autism [J].
Anney, Richard ;
Klei, Lambertus ;
Pinto, Dalila ;
Regan, Regina ;
Conroy, Judith ;
Magalhaes, Tiago R. ;
Correia, Catarina ;
Abrahams, Brett S. ;
Sykes, Nuala ;
Pagnamenta, Alistair T. ;
Almeida, Joana ;
Bacchelli, Elena ;
Bailey, Anthony J. ;
Baird, Gillian ;
Battaglia, Agatino ;
Berney, Tom ;
Bolshakova, Nadia ;
Boelte, Sven ;
Bolton, Patrick F. ;
Bourgeron, Thomas ;
Brennan, Sean ;
Brian, Jessica ;
Carson, Andrew R. ;
Casallo, Guillermo ;
Casey, Jillian ;
Chu, Su H. ;
Cochrane, Lynne ;
Corsello, Christina ;
Crawford, Emily L. ;
Crossett, Andrew ;
Dawson, Geraldine ;
de Jonge, Maretha ;
Delorme, Richard ;
Drmic, Irene ;
Duketis, Eftichia ;
Duque, Frederico ;
Estes, Annette ;
Farrar, Penny ;
Fernandez, Bridget A. ;
Folstein, Susan E. ;
Fombonne, Eric ;
Freitag, Christine M. ;
Gilbert, John ;
Gillberg, Christopher ;
Glessner, Joseph T. ;
Goldberg, Jeremy ;
Green, Jonathan ;
Guter, Stephen J. ;
Hakonarson, Hakon ;
Heron, Elizabeth A. .
HUMAN MOLECULAR GENETICS, 2010, 19 (20) :4072-4082
[4]   Association between polymorphisms in the promoter region of the sialyltransferase 8B (SIAT8B) gene and schizophrenia [J].
Arai, M ;
Yamada, K ;
Toyota, T ;
Obata, N ;
Haga, S ;
Yoshida, Y ;
Nakamura, K ;
Minabe, Y ;
Ujike, H ;
Sora, I ;
Ikeda, K ;
Mori, N ;
Yoshikawa, T ;
Itokawa, M .
BIOLOGICAL PSYCHIATRY, 2006, 59 (07) :652-659
[5]   DECREASED EXPRESSION OF THE EMBRYONIC FORM OF THE NEURAL CELL-ADHESION MOLECULE IN SCHIZOPHRENIC BRAINS [J].
BARBEAU, D ;
LIANG, JJ ;
ROBITAILLE, Y ;
QUIRION, R ;
SRIVASTAVA, LK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (07) :2785-2789
[6]  
Barde Y A, 1994, Prog Clin Biol Res, V390, P45
[7]   PURIFICATION OF A NEW NEUROTROPHIC FACTOR FROM MAMMALIAN BRAIN [J].
BARDE, YA ;
EDGAR, D ;
THOENEN, H .
EMBO JOURNAL, 1982, 1 (05) :549-553
[8]   PSA-NCAM in mammalian structural plasticity and neurogenesis [J].
Bonfanti, Luca .
PROGRESS IN NEUROBIOLOGY, 2006, 80 (03) :129-164
[9]   Brain-derived neurotrophic factor: findings in schizophrenia [J].
Buckley, Peter F. ;
Pillai, Anilkumar ;
Howell, Kristy R. .
CURRENT OPINION IN PSYCHIATRY, 2011, 24 (02) :122-127
[10]   Pharmacokinetics and pharmacodynamics of recombinant FGF-2 in a phase I trial in coronary artery disease [J].
Bush, MA ;
Samara, E ;
Whitehouse, MJ ;
Yoshizawa, C ;
Novicki, DL ;
Pike, M ;
Laham, RJ ;
Simons, M ;
Chronos, NA .
JOURNAL OF CLINICAL PHARMACOLOGY, 2001, 41 (04) :378-385