Hyaluronan in morphogenesis

被引:422
作者
Tool, BP [1 ]
机构
[1] Tufts Univ, Sch Med, Dept Anat & Cell Biol, Boston, MA 02111 USA
关键词
hyaluronan; pericellular matrix; hyaladherins; hyaluronan synthase; cell signaling;
D O I
10.1006/scdb.2000.0244
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Hyaluronan is a very large polysaccharide that is found in extracellular matrices, at the cell surface and inside cells. This review focuses on the functions of hyaluronan directly associated with the cell surface where it is commonly present as the essential core of a highly hydrated pericellular matrix that contains several other components (hydraladherins) bound to hyaluronan. Three major molecular characteristics of hyaluronan contribute to its physiological functions: its unique hydrodynamic properties, its interactions with structural extracellular hyaladherins, and its instructive effects on cell signaling and behavior. Recent studies of hyaluronan-deficient mouse embryos illustrate the importance of each of these classes of function of hyaluronan. It is postulated that the morphogenetic effects of hyaluronan are due to its ability to act as a template for assembly of a multi-component, pericellular matrix as well as to its physical properties. This matrix would provide a hydrated environment in which cells are separated from structural barriers to morphogenetic changes and receive signals from hyaluronan itself and from associated factors.
引用
收藏
页码:79 / 87
页数:9
相关论文
共 87 条
[11]   Interaction between the adhesion receptor, CD44, and the oncogene product, p185(HER2), promotes human ovarian tumor cell activation [J].
Bourguignon, LYW ;
Zhu, HB ;
Chu, A ;
Iida, N ;
Zhang, L ;
Hung, MC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (44) :27913-27918
[12]   CD44 interaction with Tiam1 promotes Rac1 signaling and hyaluronic acid-mediated breast tumor cell migration [J].
Bourguignon, LYW ;
Zhu, HB ;
Shao, LJ ;
Chen, YW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (03) :1829-1838
[13]   INCREASED HYALURONATE SYNTHESIS IS REQUIRED FOR FIBROBLAST DETACHMENT AND MITOSIS [J].
BRECHT, M ;
MAYER, U ;
SCHLOSSER, E ;
PREHM, P .
BIOCHEMICAL JOURNAL, 1986, 239 (02) :445-450
[14]   Disruption of hyaluronan synthase-2 abrogates normal cardiac morphogenesis and hyaluronan-mediated transformation of epithelium to mesenchyme [J].
Camenisch, TD ;
Spicer, AP ;
Brehm-Gibson, T ;
Biesterfeldt, J ;
Augustine, ML ;
Calabro, A ;
Kubalak, S ;
Klewer, SE ;
McDonald, JA .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 106 (03) :349-360
[15]  
CHEN L, 1994, J BIOL CHEM, V269, P28282
[16]   Rapid hyaluronan uptake is associated with enhanced motility: implications for an intracellular mode of action [J].
Collis, L ;
Hall, C ;
Lange, L ;
Ziebell, M ;
Prestwich, R ;
Turley, EA .
FEBS LETTERS, 1998, 440 (03) :444-449
[17]   Hyaluronan synthases: fascinating glycosyltransferases from vertebrates, bacterial pathogens, and algal viruses [J].
DeAngelis, PL .
CELLULAR AND MOLECULAR LIFE SCIENCES, 1999, 56 (7-8) :670-682
[18]   Molecular cloning of human fibroblast hyaluronic acid-binding protein confirms its identity with P-32, a protein co-purified with splicing factor SF2 - Kyaluronic acid-binding protein as P-32 protein, co-purified with splicing factor SF2 [J].
Deb, TB ;
Datta, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (04) :2206-2212
[19]  
Ellis I, 1997, DEVELOPMENT, V124, P1593
[20]  
Entwistle J, 1996, J CELL BIOCHEM, V61, P569, DOI 10.1002/(SICI)1097-4644(19960616)61:4<569::AID-JCB10>3.0.CO