A NOVEL TARGET-CELL FOR C-FOS-INDUCED ONCOGENESIS - DEVELOPMENT OF CHONDROGENIC TUMORS IN EMBRYONIC STEM-CELL CHIMERAS

被引:156
作者
WANG, ZQ
GRIGORIADIS, AE
MOHLESTEINLEIN, U
WAGNER, EF
机构
[1] Resch Ins of Molec Pathology, A-1030 Vienna
关键词
ES CELLS; CHIMERAS; CARTILAGE; CELL LINES; TRANSFORMATION;
D O I
10.1002/j.1460-2075.1991.tb07783.x
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
Embryonic stem (ES) cells were used to investigate the target cell specificity and consequences of c-fos when expressed ectopically during embryonic development. Chimeric mice generated with different ES cell clones selected for high exogenous c-fos expression were not affected during embryonic development; however, a high frequency of cartilage tumours developed as early as 3-4 weeks of age apparently independent of the extent of chimerism. The tumours originated from cartilagenous tissues and contained many chondrocytes. Expression of exogenous c-fos RNA and Fos protein was observed during development but was highest in tumour tissues, predominantly in differentiating chondrocytes. A number of primary and clonal tumour-derived cell lines were established which expressed high levels of c-fos, c-jun as well as the cartilage-specific gene type II collagen and which gave rise to cartilage tumours in vivo, some of which also contained bone. Interestingly, the levels of c-Fos and c-Jun appeared to be coordinately regulated in the cell lines as well as in chimeric tissues. Thus, we demonstrate that chondrogenic cells and earlier progenitors are specifically transformed by Fos/Jun and therefore represent a novel mesenchymal target cell for c-fos overexpression.
引用
收藏
页码:2437 / 2450
页数:14
相关论文
共 64 条
[11]   TRANSCRIPTION FACTOR INTERACTIONS - SELECTORS OF POSITIVE OR NEGATIVE REGULATION FROM A SINGLE DNA ELEMENT [J].
DIAMOND, MI ;
MINER, JN ;
YOSHINAGA, SK ;
YAMAMOTO, KR .
SCIENCE, 1990, 249 (4974) :1266-1272
[12]   NUCLEOPROTEIN COMPLEXES THAT REGULATE GENE-EXPRESSION IN ADIPOCYTE DIFFERENTIATION - DIRECT PARTICIPATION OF C-FOS [J].
DISTEL, RJ ;
RO, HS ;
ROSEN, BS ;
GROVES, DL ;
SPIEGELMAN, BM .
CELL, 1987, 49 (06) :835-844
[13]   PROTOONCOGENE C-FOS EXPRESSION IN GROWTH REGIONS OF FETAL BONE AND MESODERMAL WEB TISSUE [J].
DONY, C ;
GRUSS, P .
NATURE, 1987, 328 (6132) :711-714
[14]   VIRUS INDUCTION OF OSTEOSARCOMAS IN MICE [J].
FINKEL, MP ;
BISKIS, BO ;
JINKINS, PB .
SCIENCE, 1966, 151 (3711) :698-&
[15]  
FINKEL MP, 1975, FRONTIERS RADIATION, V10, P28
[16]   THE FOS COMPLEX AND FOS-RELATED ANTIGENS RECOGNIZE SEQUENCE ELEMENTS THAT CONTAIN AP-1 BINDING-SITES [J].
FRANZA, BR ;
RAUSCHER, FJ ;
JOSEPHS, SF ;
CURRAN, T .
SCIENCE, 1988, 239 (4844) :1150-1153
[17]   CHARACTERIZATION OF FOS-INDUCED OSTEOGENIC TUMORS AND TUMOR-DERIVED MURINE CELL-LINES [J].
GORALCZYK, R ;
CLOSS, EI ;
RUTHER, U ;
WAGNER, EF ;
STRAUSS, PG ;
ERFLE, V ;
SCHMIDT, J .
DIFFERENTIATION, 1990, 44 (02) :122-131
[18]   CONTINUOUSLY GROWING BIPOTENTIAL AND MONOPOTENTIAL MYOGENIC, ADIPOGENIC, AND CHONDROGENIC SUBCLONES ISOLATED FROM THE MULTIPOTENTIAL RCJ 3.1 CLONAL CELL-LINE [J].
GRIGORIADIS, AE ;
HEERSCHE, JNM ;
AUBIN, JE .
DEVELOPMENTAL BIOLOGY, 1990, 142 (02) :313-318
[19]   DIFFERENTIATION OF MUSCLE, FAT, CARTILAGE, AND BONE FROM PROGENITOR CELLS PRESENT IN A BONE-DERIVED CLONAL CELL-POPULATION - EFFECT OF DEXAMETHASONE [J].
GRIGORIADIS, AE ;
HEERSCHE, JNM ;
AUBIN, JE .
JOURNAL OF CELL BIOLOGY, 1988, 106 (06) :2139-2151
[20]  
HANAHAN D, 1988, ANNU REV GENET, V22, P479, DOI 10.1146/annurev.ge.22.120188.002403