Selective effects of sodium chlorate treatment on the sulfation of heparan sulfate

被引:141
作者
Safaiyan, F
Kolset, SO
Prydz, K
Gottfridsson, E
Lindahl, U
Salmivirta, M
机构
[1] Univ Uppsala, Ctr Biomed, Dept Med Biochem & Microbiol, S-75123 Uppsala, Sweden
[2] Univ Oslo, Inst Nutr Res, N-0316 Oslo, Norway
[3] Univ Oslo, Dept Biochem, N-0316 Oslo, Norway
关键词
D O I
10.1074/jbc.274.51.36267
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
We have analyzed the effect of sodium chlorate treatment of Madin-Darby canine kidney cells on the structure of heparan sulfate (HS), to assess how the various sulfation reactions during HS biosynthesis are affected by decreased availability of the sulfate donor 3'-phosphoadenosine 5'-phosphosulfate. Metabolically [H-3]glucosamine-labeled HS was isolated from chlorate-treated and untreated Madin-Darby canine kidney cells and subjected to low pH nitrous acid cleavage. Saccharides representing (i) the N-sulfated domains, (ii) the domains of alternating N-acetylated and N-sulfated disaccharide units, and (iii) the N-acetylated domains were recovered and subjected to compositional disaccharide analysis. Upon treatment with 50 mM chlorate, overall O-sulfation of HS was inhibited by similar to 70%, whereas N-sulfation remained essentially unchanged. Low chlorate concentrations (5 or 2 mM) selectively reduced the 6-O-sulfation of HS, whereas treatment with 50 mM chlorate reduced both 2-O and 6-O-sulfation. Analysis of saccharides representing the different domain types indicated that 6-O-sulfation was preferentially inhibited in the alternating domains. These data suggest that reduced 3'-phosphoadenosine 5'-phosphosulfate availability has distinct effects on the N- and O-sulfation of HS and that O-sulfation is affected in a domain-specific fashion.
引用
收藏
页码:36267 / 36273
页数:7
相关论文
共 40 条
[1]   Molecular cloning and expression of a third member of the heparan sulfate/heparin GlcNAc N-deacetylase/N-sulfotransferase family [J].
Aikawa, J ;
Esko, JD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (05) :2690-2695
[2]   BIOLOGY OF THE SYNDECANS - A FAMILY OF TRANSMEMBRANE HEPARAN-SULFATE PROTEOGLYCANS [J].
BERNFIELD, M ;
KOKENYESI, R ;
KATO, M ;
HINKES, MT ;
SPRING, J ;
GALLO, RL ;
LOSE, EJ .
ANNUAL REVIEW OF CELL BIOLOGY, 1992, 8 :365-393
[3]  
BIENKOWSKI MJ, 1985, J BIOL CHEM, V260, P356
[4]   Structural modification of fibroblast growth factor-binding heparan sulfate at a determinative stage of neural development [J].
Brickman, YG ;
Ford, MD ;
Gallagher, JT ;
Nurcombe, V ;
Bartlett, PF ;
Turnbull, JE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (08) :4350-4359
[5]   Expression of the mouse mastocytoma glucosaminyl N-deacetylase N-sulfotransferase in human kidney 293 cells results in increased N-sulfation of heparan sulfate [J].
Cheung, WF ;
Eriksson, I ;
KuscheGullberg, M ;
Lindahl, U ;
Kjellen, L .
BIOCHEMISTRY, 1996, 35 (16) :5250-5256
[6]   Heparan sulfate proteoglycans play a dual role in regulating fibroblast growth factor-2 mitogenic activity in human breast cancer cells [J].
Delehedde, M ;
Deudon, E ;
Boilly, B ;
Hondermarck, H .
EXPERIMENTAL CELL RESEARCH, 1996, 229 (02) :398-406
[7]   ATP SULFURYLASE FROM PENCILLIUM-CHRYSOGENUM .4. ADENOSINE-TRIPHOSPHATE SULFURYLASE FROM PENICILLIUM-CHRYSOGENUM - EQUILIBRIUM BINDING, SUBSTRATE HYDROLYSIS, AND ISOTOPE EXCHANGE STUDIES [J].
FARLEY, JR ;
NAKAYAMA, G ;
CRYNS, D ;
SEGEL, IH .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1978, 185 (02) :376-390
[8]   Age-dependent modulation of heparan sulfate structure and function [J].
Feyzi, E ;
Saldeen, T ;
Larsson, E ;
Lindahl, U ;
Salmivirta, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (22) :13395-13398
[9]   PATTERNS OF SULFATION IN HEPARAN-SULFATE - POLYMORPHISM BASED ON A COMMON STRUCTURAL THEME [J].
GALLAGHER, JT ;
TURNBULL, JE ;
LYON, M .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY, 1992, 24 (04) :553-560
[10]   Sulfation in high endothelial venules: cloning and expression of the human PAPS synthetase [J].
Girard, JP ;
Baekkevold, ES ;
Amalric, F .
FASEB JOURNAL, 1998, 12 (07) :603-612