CD44 PLAYS A ROLE IN ADHESIVE INTERACTIONS BETWEEN GLIOMA-CELLS AND EXTRACELLULAR-MATRIX COMPONENTS

被引:53
作者
RADOTRA, B
MCCORMICK, D
CROCKARD, A
机构
[1] QUEENS UNIV BELFAST,NEUROONCOL LAB,BELFAST BT12 6BL,NORTH IRELAND
[2] ROYAL VICTORIA HOSP,IMMUNOL LAB,BELFAST BT12 6BA,NORTH IRELAND
关键词
CD44; GLIOMA; INVASION; EXTRACELLULAR MATRIX;
D O I
10.1111/j.1365-2990.1994.tb00986.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Glioma invasion is a complex process involving interactions of tumour cells with host cells and extracellular matrix (ECM). The initial event in the process is recognition and attachment of glioma cells to specific ECM molecules prior to migration into proteolytically modified matrix. In comparison with other tissues, brain ECM is a relatively amorphous matrix which contains glycosaminoglycans including hyaluronan (HA). Recently CD44 which is a transmembrane adhesion molecule found on a wide variety of cells, has been suggested as the principal cell surface receptor for HA, In the present in vitro investigation we have analysed the role of CD44 in adhesive interactions between human gliomas and ECM. Our experimental procedures included immunocytochemistry, immunoblotting, in vitro adhesion assay and now cytometry. CD44 was expressed on the surface of all gliomas analysed (9) and the level of expression showed no correlation with tumour grade. Eighty, 95 and 120 kDa isoforms were demonstrated by immunoblotting. In an adhesion blocking assay it was found that ligation of CD44 with specific antibody resulted in reduced adhesion to hyaluronan, chondroitin sulphate, fibronectin, laminin, collagen IV and Matrigel(TM). We conclude that CD44 is involved in adhesion of glioma cells to a wide range of ECM components.
引用
收藏
页码:399 / 405
页数:7
相关论文
共 35 条
[21]  
KLEIHUES P, 1993, HISTOLOGICAL TYPING, P9
[22]   ISOLATION AND CHARACTERIZATION OF TYPE-IV PROCOLLAGEN, LAMININ, AND HEPARAN-SULFATE PROTEOGLYCAN FROM THE EHS SARCOMA [J].
KLEINMAN, HK ;
MCGARVEY, ML ;
LIOTTA, LA ;
ROBEY, PG ;
TRYGGVASON, K ;
MARTIN, GR .
BIOCHEMISTRY, 1982, 21 (24) :6188-6193
[23]  
KUPPNER MC, 1990, CLIN EXP IMMUNOL, V81, P142
[24]   DIFFERENTIAL EXPRESSION OF THE CD44 MOLECULE IN HUMAN BRAIN-TUMORS [J].
KUPPNER, MC ;
VAN MEIR, E ;
GAUTHIER, T ;
HAMOU, MF ;
DETRIBOLET, N .
INTERNATIONAL JOURNAL OF CANCER, 1992, 50 (04) :572-577
[25]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[26]   CD44 AND ITS INTERACTION WITH EXTRACELLULAR-MATRIX [J].
LESLEY, J ;
HYMAN, R ;
KINCADE, PW .
ADVANCES IN IMMUNOLOGY, VOL 54, 1993, 54 :271-335
[27]  
LI H, 1993, CANCER RES, V53, P5345
[28]   CD44 EXPRESSION IN HUMAN ASTROCYTES AND OLIGODENDROCYTES IN CULTURE [J].
MORETTO, G ;
XU, RY ;
KIM, SU .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1993, 52 (04) :419-423
[29]  
PICKER LJ, 1989, J IMMUNOL, V142, P2046
[30]   DIFFERENTIAL BINDING OF ANTI-CD44 ON HUMAN GLIOMAS INVITRO [J].
PILKINGTON, GJ ;
AKINWUNMI, J ;
OGNJENOVIC, N ;
ROGERS, JP .
NEUROREPORT, 1993, 4 (03) :259-262