DIFFERENTIAL EXPRESSION OF MULTIPLE CELL-SURFACE HEPARAN-SULFATE PROTEOGLYCANS DURING EMBRYONIC TOOTH DEVELOPMENT

被引:47
作者
BAI, XM [1 ]
VANDERSCHUEREN, B [1 ]
CASSIMAN, JJ [1 ]
VANDENBERGHE, H [1 ]
DAVID, G [1 ]
机构
[1] CATHOLIC UNIV LEUVEN,CTR HUMAN GENET,B-3000 LOUVAIN,BELGIUM
关键词
HEPARAN SULFATE; SYNDECAN-1; FIBROGLYCAN; TOOTH DEVELOPMENT;
D O I
10.1177/42.8.8027524
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Heparan sulfate accumulates on cell surfaces and at cell-matrix interfaces, and functionally modulates several of the effector molecules that support the interactions, growth, and differentiation of developing tissues. Using heparan sulfate-specific monoclonal antibodies MAb, we obtained evidence that extracts from rodent embryos contain multiple forms of cell surface-associated heparan sulfate proteoglycan (PG). Taking tooth development in the mouse embryo as a model to further investigate the relevance of this PG redundancy and using MAb against heparan sulfate, antibodies specific for syndecan (syndecan-1) and fibroglycan (syndecan-2) (two distinct members of a larger family of cell-surface heparan sulfate PGs), and specific cDNA probes for these two cell-surface PGs, we obtained in situ evidence for regulated and differential expression of multiple cell-surface heparan sulfate PGs. The unique, distinctive, and coordinated changes in the expressions of these PGs during morphogenesis and differentiation of dental tissues suggest that the various cell-surface PGs are not truly redundant but play important, specific, and potentially complementary roles during embryonic development.
引用
收藏
页码:1043 / 1054
页数:12
相关论文
共 45 条
[1]  
BEGUEKIRN C, 1992, INT J DEV BIOL, V36, P491
[2]   SYNDECAN, A DEVELOPMENTALLY REGULATED CELL-SURFACE PROTEOGLYCAN THAT BINDS EXTRACELLULAR-MATRIX AND GROWTH-FACTORS [J].
BERNFIELD, M ;
SANDERSON, RD .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1990, 327 (1239) :171-186
[3]   SYNDECAN, A CELL-SURFACE PROTEOGLYCAN, EXHIBITS A MOLECULAR POLYMORPHISM DURING LUNG DEVELOPMENT [J].
BRAUKER, JH ;
TRAUTMAN, MS ;
BERNFIELD, M .
DEVELOPMENTAL BIOLOGY, 1991, 147 (02) :285-292
[4]   IMMUNOLOCALIZATION OF TRANSFORMING GROWTH FACTOR-BETA-1 AND EPIDERMAL GROWTH-FACTOR RECEPTOR EPITOPES IN MOUSE INCISORS AND MOLARS WITH A DEMONSTRATION OF INVITRO PRODUCTION OF TRANSFORMING ACTIVITY [J].
CAM, Y ;
NEUMANN, MR ;
RUCH, JV .
ARCHIVES OF ORAL BIOLOGY, 1990, 35 (10) :813-822
[5]  
CAM Y, 1992, INT J DEV BIOL, V36, P381
[6]   MOLECULAR-CLONING AND CHARACTERIZATION OF N-SYNDECAN, A NOVEL TRANSMEMBRANE HEPARAN-SULFATE PROTEOGLYCAN [J].
CAREY, DJ ;
EVANS, DM ;
STAHL, RC ;
ASUNDI, VK ;
CONNER, KJ ;
GARBES, P ;
CIZMECISMITH, G .
JOURNAL OF CELL BIOLOGY, 1992, 117 (01) :191-201
[7]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[8]   DEVELOPMENTAL-CHANGES IN HEPARAN-SULFATE EXPRESSION - INSITU DETECTION WITH MABS [J].
DAVID, G ;
BAI, XM ;
VANDERSCHUEREN, B ;
CASSIMAN, JJ ;
VANDENBERGHE, H .
JOURNAL OF CELL BIOLOGY, 1992, 119 (04) :961-975
[9]  
DAVID G, 1993, DEVELOPMENT, V119, P841
[10]   MOLECULAR-CLONING OF A PHOSPHATIDYLINOSITOL-ANCHORED MEMBRANE HEPARAN-SULFATE PROTEOGLYCAN FROM HUMAN LUNG FIBROBLASTS [J].
DAVID, G ;
LORIES, V ;
DECOCK, B ;
MARYNEN, P ;
CASSIMAN, JJ ;
VANDENBERGHE, H .
JOURNAL OF CELL BIOLOGY, 1990, 111 (06) :3165-3176