Internalization of the hyaluronan receptor CD44 by chondrocytes

被引:83
作者
Aguiar, DJ [1 ]
Knudson, W [1 ]
Knudson, CB [1 ]
机构
[1] Rush Med Coll, Rush Presbyterian St Lukes Med Ctr, Dept Biochem, Chicago, IL 60612 USA
关键词
chondrocyte; hyaluronan; CD44; hyaladherins; proteoglycans;
D O I
10.1006/excr.1999.4641
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chondrocytes express CD44 as a primary receptor for the matrix macromolecule hyaluronan. Hyaluronan is responsible for the retention and organization of proteoglycan within cartilage, and hyaluronan-chondrocyte interactions are important for the assembly and maintenance of the cartilage matrix. Bovine articular chondrocytes were used to study the endocytosis and turnover of CD44 and the effects of receptor occupancy on this turnover. Matrix-intact chondrocytes exhibit approximately a 6% internalization of cell surface CD44 by 4 h. Treatment with Streptomyces hyaluronidase to remove endogenous pericellular matrix increased internalization to approximately 20% of cell surface CD44 at 4 h. This turnover could be partially inhibited by the addition of exogenous hyaluronan to these matrix-depleted chondrocytes. Cell surface biotin-labeled CD44 was internalized by chondrocytes and this internalization was decreased in the presence of hyaluronan. Colocalization of internalized CD44 and fluorescein-labeled hyaluronan in intracellular vesicles correlates with the previous results of receptor-mediated endocytosis pathway for the degradation of hyaluronan by acid hydrolases. Taken together, our results indicate that CD44 is internalized by chondrocytes and that CD44 turnover is modulated by occupancy with hyaluronan. (C) 1999 Academic Press.
引用
收藏
页码:292 / 302
页数:11
相关论文
共 44 条
[1]  
AGUIAR DJ, 1996, T ORTHO RES SOC, V21, P86
[2]   SUBCELLULAR-LOCALIZATION OF MOESIN IN DYNAMIC FILOPODIA, RETRACTION FIBERS, AND OTHER STRUCTURES INVOLVED IN SUBSTRATE EXPLORATION, ATTACHMENT, AND CELL-CELL CONTACTS [J].
AMIEVA, MR ;
FURTHMAYR, H .
EXPERIMENTAL CELL RESEARCH, 1995, 219 (01) :180-196
[3]   REPLACEMENT OF THE PHOSPHOLIPID-ANCHOR IN THE CONTACT SITE-A GLYCOPROTEIN OF D-DISCOIDEUM BY A TRANSMEMBRANE REGION DOES NOT IMPEDE CELL-ADHESION BUT REDUCES RESIDENCE TIME ON THE CELL-SURFACE [J].
BARTH, A ;
MULLERTAUBENBERGER, A ;
TARANTO, P ;
GERISCH, G .
JOURNAL OF CELL BIOLOGY, 1994, 124 (1-2) :205-215
[4]   MEDIATORS AND AUTOPATHOGENIC EFFECTOR-CELLS IN PROTEOGLYCAN-INDUCED ARTHRITIC AND CLINICALLY ASYMPTOMATIC BALB/C MICE [J].
BUZAS, EI ;
MIKECZ, K ;
BRENNAN, FR ;
GLANT, TT .
CELLULAR IMMUNOLOGY, 1994, 158 (02) :292-304
[5]   INCREASED EXPRESSION OF CD44 IN BOVINE ARTICULAR CHONDROCYTES BY CATABOLIC CELLULAR MEDIATORS [J].
CHOW, G ;
KNUDSON, CB ;
HOMANDBERG, G ;
KNUDSON, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (46) :27734-27741
[6]  
Chow G, 1998, ARTHRITIS RHEUM-US, V41, P1411, DOI 10.1002/1529-0131(199808)41:8<1411::AID-ART10>3.0.CO
[7]  
2-Z
[8]   Ligand-induced changes in integrin expression regulate neuronal adhesion and neurite outgrowth [J].
Condic, ML ;
Letourneau, PC .
NATURE, 1997, 389 (6653) :852-856
[9]   THE HYALURONAN RECEPTOR (CD44) PARTICIPATES IN THE UPTAKE AND DEGRADATION OF HYALURONAN [J].
CULTY, M ;
NGUYEN, HA ;
UNDERHILL, CB .
JOURNAL OF CELL BIOLOGY, 1992, 116 (04) :1055-1062
[10]   CELL-ADHESION TO EXTRACELLULAR-MATRIX REGULATES THE LIFE-CYCLE OF INTEGRINS [J].
DALTON, SL ;
SCHARF, E ;
BRIESEWITZ, R ;
MARCANTONIO, EE ;
ASSOIAN, RK .
MOLECULAR BIOLOGY OF THE CELL, 1995, 6 (12) :1781-1791