Heparan sulfate proteoglycans on the cell surface: versatile coordinators of cellular functions

被引:304
作者
Tumova, S [1 ]
Woods, A [1 ]
Couchman, JR [1 ]
机构
[1] Univ Alabama Birmingham, Dept Cell Biol, Cell Adhes & Matrix Res Ctr, Birmingham, AL 35294 USA
关键词
heparan sulfate proteoglycan; syndecan; glypican; adhesion; development;
D O I
10.1016/S1357-2725(99)00116-8
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
Heparan sulfate proteoglycans are complex molecules composed of a core protein with covalently attached glycosaminoglycan chains. While the protein part determines localization of the proteoglycan on the cell surfaces or in the extracellular matrix, the glycosaminoglycan component, heparan sulfate, mediates interactions with a variety of extracellular ligands such as growth factors and adhesion molecules. Through these interactions, heparan sulfate proteoglycans participate in many events during cell adhesion, migration, proliferation and differentiation. We are determining the multitude of proteoglycan functions, as their intricate roles in many pathways are revealed. They act as coreceptors for growth factors, participate in signalling during cell adhesion, modulate the activity of a broad range of molecules, and partake in many developmental and pathological processes. including tumorigenesis and wound repair. This review concentrates on biological roles of cell surface heparan sulfate proteoglycans, namely syndecans and glypicans, and outlines the progress achieved during the last decade in unraveling the molecular interactions behind proteoglycan functions. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:269 / 288
页数:20
相关论文
共 153 条
[71]   LOSS OF CELL-SURFACE SYNDECAN-1 CAUSES EPITHELIA TO TRANSFORM INTO ANCHORAGE-INDEPENDENT MESENCHYME-LIKE CELLS [J].
KATO, M ;
SAUNDERS, S ;
NGUYEN, H ;
BERNFIELD, M .
MOLECULAR BIOLOGY OF THE CELL, 1995, 6 (05) :559-576
[72]   Physiological degradation converts the soluble syndecan-1 ectodomain from an inhibitor to a potent activator of FGF-2 [J].
Kato, M ;
Wang, HM ;
Kainulainen, V ;
Fitzgerald, ML ;
Ledbetter, S ;
Ornitz, DM ;
Bernfield, M .
NATURE MEDICINE, 1998, 4 (06) :691-697
[73]   MEMBERS OF THE SYNDECAN FAMILY OF HEPARAN-SULFATE PROTEOGLYCANS ARE EXPRESSED IN DISTINCT CELL-SPECIFIC, TISSUE-SPECIFIC, AND DEVELOPMENT-SPECIFIC PATTERNS [J].
KIM, CW ;
GOLDBERGER, OA ;
GALLO, RL ;
BERNFIELD, M .
MOLECULAR BIOLOGY OF THE CELL, 1994, 5 (07) :797-805
[74]   Cortactin-Src kinase signaling pathway is involved in N-syndecan-dependent neurite outgrowth [J].
Kinnunen, T ;
Kaksonen, M ;
Saarinen, J ;
Kalkkinen, N ;
Peng, HB ;
Rauvala, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (17) :10702-10708
[75]   PROTEOGLYCANS - STRUCTURES AND INTERACTIONS [J].
KJELLEN, L ;
LINDAHL, U .
ANNUAL REVIEW OF BIOCHEMISTRY, 1991, 60 :443-475
[76]   The cell-surface heparan sulfate proteoglycan glypican-1 regulates growth factor action in pancreatic carcinoma cells and is overexpressed in human pancreatic cancer [J].
Kleeff, J ;
Ishiwata, T ;
Kumbasar, A ;
Friess, H ;
Buchler, MW ;
Lander, AD ;
Korc, M .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (09) :1662-1673
[77]  
KOJIMA T, 1992, J BIOL CHEM, V267, P4859
[78]   Proteoglycans: Master regulators of molecular encounter? [J].
Lander, AD .
MATRIX BIOLOGY, 1998, 17 (07) :465-472
[79]   Multiple heparan sulfate chains are required for optimal syndecan-1 function [J].
Langford, JK ;
Stanley, MJ ;
Cao, DJ ;
Sanderson, RD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (45) :29965-29971
[80]   Solution structure of a syndecan-4 cytoplasmic domain and its interaction with phosphatidylinositol 4,5-bisphosphate [J].
Lee, D ;
Oh, ES ;
Woods, A ;
Couchman, JR ;
Lee, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (21) :13022-13029