ROLE OF THE 21-KDA PROTEIN TIMP-3 IN ONCOGENIC TRANSFORMATION OF CULTURED CHICKEN-EMBRYO FIBROBLASTS

被引:147
作者
YANG, TT
HAWKES, SP
机构
[1] UNIV CALIF SAN FRANCISCO,DEPT PHARM,DIV TOXICOL,SAN FRANCISCO,CA 94143
[2] UNIV CALIF SAN FRANCISCO,DEPT PHARMACEUT CHEM,DIV TOXICOL,SAN FRANCISCO,CA 94143
关键词
D O I
10.1073/pnas.89.22.10676
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The 21-kDa protein is an extracellular matrix (ECM) component whose synthesis is stimulated transiently during oncogenic transformation of chicken embryo fibroblasts (CEF) or after treatment of normal cells with the tumor promoter phorbol 12-myristate 13-acetate. Biochemical characterization indicates that the protein is related, but not identical, to two members of the family of tissue inhibitors of metalloproteinases, TIMP-1 and TIMP-2. The cDNA of the 21-kDa protein was recently cloned, and based upon its deduced amino acid sequence and other supporting data we propose that it is another member of this family, a TIMP-3. We now report electrophoretic purification of sufficient quantities of this protein to determine its function. The protein promotes the detachment of transforming cells from the ECM. Although its presence in the matrix may be necessary for cell release it is not the only factor involved because it does not influence the adhesive properties of nontransformed cells. It also appears to accelerate the morphological changes associated with cell transformation and stimulates the proliferation of growth-retarded, nontransformed cells maintained under low serum conditions. Based on these data we hypothesize that the 21-kDa protein promotes the development of the transformed phenotype in cultured cells.
引用
收藏
页码:10676 / 10680
页数:5
相关论文
共 45 条
[1]   CELL DETACHMENT MEDIATED BY HYALURONIC-ACID [J].
ABATANGELO, G ;
CORTIVO, R ;
MARTELLI, M ;
VECCHIA, P .
EXPERIMENTAL CELL RESEARCH, 1982, 137 (01) :73-78
[2]  
AVALOS BR, 1988, BLOOD, V71, P1721
[3]   GROWTH-STIMULATION OF HUMAN KERATINOCYTES BY TISSUE INHIBITOR OF METALLOPROTEINASES [J].
BERTAUX, B ;
HORNEBECK, W ;
EISEN, AZ ;
DUBERTRET, L .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1991, 97 (04) :679-685
[4]  
BERTAUX B, 1990, PATHOL BIOL, V38, P1029
[5]   TRANSFORMATION-SENSITIVE PROTEIN ASSOCIATED WITH THE CELL SUBSTRATUM OF CHICKEN-EMBRYO FIBROBLASTS [J].
BLENIS, J ;
HAWKES, SP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (03) :770-774
[6]  
BLENIS J, 1984, J BIOL CHEM, V259, P1563
[7]   FIBRONECTIN-DEGRADING PROTEASES FROM THE MEMBRANES OF TRANSFORMED-CELLS [J].
CHEN, JM ;
CHEN, WT .
CELL, 1987, 48 (02) :193-203
[8]   LOCAL DEGRADATION OF FIBRONECTIN AT SITES OF EXPRESSION OF THE TRANSFORMING GENE-PRODUCT PP60SRC [J].
CHEN, WT ;
CHEN, JM ;
PARSONS, SJ ;
PARSONS, JT .
NATURE, 1985, 316 (6024) :156-158
[9]   ENHANCEMENT OF TRANSFORMED-CELL GROWTH IN AGAR BY SERINE PROTEASE INHIBITORS [J].
COOK, JR ;
CHEN, JK .
JOURNAL OF CELLULAR PHYSIOLOGY, 1988, 136 (01) :188-193
[10]   SEQUENCE OF HUMAN-TISSUE INHIBITOR OF METALLOPROTEINASES AND ITS IDENTITY TO ERYTHROID-POTENTIATING ACTIVITY [J].
DOCHERTY, AJP ;
LYONS, A ;
SMITH, BJ ;
WRIGHT, EM ;
STEPHENS, PE ;
HARRIS, TJR ;
MURPHY, G ;
REYNOLDS, JJ .
NATURE, 1985, 318 (6041) :66-69