Chemical and immunological assay of the nonreducing terminal residues of chondroitin sulfate from human aggrecan

被引:121
作者
Plaas, AHK
WongPalms, S
Roughley, PJ
Midura, RJ
Hascall, VC
机构
[1] UNIV S FLORIDA,SCH MED,DEPT BIOCHEM & MOL BIOL,TAMPA,FL 33612
[2] SHRINERS HOSP CRIPPLED CHILDREN,GENET UNIT,MONTREAL,PQ H3G 1A6,CANADA
[3] CLEVELAND CLIN FDN,DEPT BIOMED ENGN,CLEVELAND,OH 44106
关键词
D O I
10.1074/jbc.272.33.20603
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
Samples of aggrecan chondroitin sulfate, isolated from normal human knee cartilages of individuals from fetal to 72 years of age, were digested with chondroitin lyases, The products were analyzed by fluorescence-based anion exchange high performance liquid chromatography to separate and quantitate nonreducing terminal structures, in addition to internal unsaturated disaccharide products, The predominant terminal structures mere the monosaccharides, GalNAc4S and GalNAc4,6S as they were present on 85-90% of all chains. The remaining chains terminated with the disaccharides GlcA beta 1,3GalNAc4S and GlcA beta 1,3GalNAc6S. Marked changes in the relative abundance of these terminals were identified in the transition from growth cartilage to adult articular cartilage, First, terminal GalNAc residues were almost exclusively 4-sulfated in aggrecan from fetal through 15 years of age, but were similar to 50% 4,6-disulfated in aggrecans from adults (22-72 years of age). Second, the terminal disaccharide GlcA beta 1,3GalNAc4S was on similar to 7% of chains on aggrecan from fetal through 15 years of age, but on only similar to 3% of chains on adult aggrecan. In contrast, the proportion of chains terminating in GlcA beta 1,3GalNAc6S, similar to 9%, was unchanged from fetal to 72 years of age, This terminal disaccharide is proposed to be recognized by the widely used monoclonal antibody 3B3, However, chemical quantitation of the structure together with solid phase 3B3(-) immunoassay of fetal and adult aggrecans showed that the content of the terminal disaccharide does not necessarily correlate with immunoreactivity of the proteoglycan, as chain density and presentation on the solid phase are critical factors for recognition of chain terminals by 3B3. The quantitative results obtained from chemical analyses of all nonreducing termini of aggrecan chondroitin sulfate chains revealed important changes in chain termination that occur when cellular activities are altered as adult articular cartilage is formed after removal of growth cartilage, These findings are discussed in relation to specific enzymatic steps that generate the nonreducing termini of chains in the biosynthesis pathway of chondroitin sulfate proteoglycans and their modulation in tissue development and pathology.
引用
收藏
页码:20603 / 20610
页数:8
相关论文
共 42 条
[1]  
Archer CW, 1996, J ANAT, V189, P23
[2]   AN UNSULFATED REGION OF THE RAT CHONDROSARCOMA CHONDROITIN SULFATE CHAIN AND ITS BINDING TO MONOCLONAL-ANTIBODY 3B3 [J].
BAKER, JR ;
CHRISTNER, JE ;
EKBORG, SL .
BIOCHEMICAL JOURNAL, 1991, 273 :237-239
[3]   Chondroitin sulphation in human joint tissues varies with age, zone and topography [J].
Bayliss, MT ;
Davidson, C ;
Woodhouse, SM ;
Osborne, DJ .
ACTA ORTHOPAEDICA SCANDINAVICA, 1995, 66 :22-25
[4]   A MOLECULAR-MODEL OF PROTEOGLYCAN-ASSOCIATED ELECTROSTATIC FORCES IN CARTILAGE MECHANICS [J].
BUSCHMANN, MD ;
GRODZINSKY, AJ .
JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME, 1995, 117 (02) :179-192
[5]   IMMUNOLOCATION ANALYSIS OF GLYCOSAMINOGLYCANS IN THE HUMAN GROWTH PLATE [J].
BYERS, S ;
CATERSON, B ;
HOPWOOD, JJ ;
FOSTER, BK .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1992, 40 (02) :275-282
[6]  
CARDOSO LEM, 1992, LAB INVEST, V67, P588
[7]   OSTEOARTHRITIS IN CYNOMOLGUS MACAQUES .2. DETECTION OF MODULATED PROTEOGLYCAN EPITOPES IN CARTILAGE AND SYNOVIAL-FLUID [J].
CARLSON, CS ;
LOESER, RF ;
JOHNSTONE, B ;
TULLI, HM ;
DOBSON, DB ;
CATERSON, B .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1995, 13 (03) :399-409
[8]  
CATERSON B, 1990, J CELL SCI, V97, P411
[9]  
CATERSON B, 1995, OSTEOARTHRITIC DISOR, P315
[10]  
CHRISTNER JE, 1980, J BIOL CHEM, V255, P7102