RAPID INDUCTION OF COMPETENCE FORMATION IS PDGF-ISOFORM SPECIFIC

被引:12
作者
COATS, SR
OLSON, JE
PLEDGER, WJ
机构
[1] Department of Cell Biology, Vanderbilt University School of Medicine, Nashville, Tennessee
[2] Abbott Laboratories, Illinois, 60064, Abbott Park
关键词
PDGF-AA AND BB; CELL CYCLE; C-MYC; FIBROBLASTS; RECEPTORS;
D O I
10.1002/jcb.240480304
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
Platelet-derived growth factor (PDGF) stimulates the expression of a number of genes associated with entry of quiescent Balb/c-3T3 fibroblasts into the cell cycle. We determined that two of these genes, c-myc and c-fos, are induced equivalently in medium supplemented with platelet-poor plasma (PPP) and either PDGF-BB or PDGF-AA. The rate at which fibroblasts entered S phase was also similar in PDGF-BB- and AA-treated cells as was the expression of the late G1 gene, thymidine kinase (TK). However, PDGF-AA must be present for a period of 16 h to stimulate the proliferation of 90% of the cells, whereas PDGF-BB was required for only 4 h. Exposure of cells to PDGF-AA for 4 h, a time during which maximum expression of c-fos and c-myc occurred, only induced 20% of the cells in a quiescent population to enter the cell cycle. Therefore, PDGF-AA-mediated expression of the immediate early genes c-fos and c-myc may be necessary but is not sufficient to rapidly stimulate density-arrested Balb/c-3T3 fibroblasts into the competent state. Thus, these data suggest that PDGF-AA and PDGF-BB initiate traverse of the cell cycle by distinct mechanisms.
引用
收藏
页码:242 / 247
页数:6
相关论文
共 35 条
[1]   ISOLATION OF A CATIONIC POLYPEPTIDE FROM HUMAN-SERUM THAT STIMULATES PROLIFERATION OF 3T3 CELLS [J].
ANTONIADES, HN ;
STATHAKOS, D ;
SCHER, CD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1975, 72 (07) :2635-2639
[2]   FUNCTIONAL-ROLE FOR C-MYC IN MITOGENIC RESPONSE TO PLATELET-DERIVED GROWTH-FACTOR [J].
ARMELIN, HA ;
ARMELIN, MCS ;
KELLY, K ;
STEWART, T ;
LEDER, P ;
COCHRAN, BH ;
STILES, CD .
NATURE, 1984, 310 (5979) :655-660
[3]   CDNA CLONING AND EXPRESSION OF A HUMAN PLATELET-DERIVED GROWTH-FACTOR (PDGF) RECEPTOR SPECIFIC FOR B-CHAIN-CONTAINING PDGF MOLECULES [J].
CLAESSONWELSH, L ;
ERIKSSON, A ;
MOREN, A ;
SEVERINSSON, L ;
EK, B ;
OSTMAN, A ;
BETSHOLTZ, C ;
HELDIN, CH .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (08) :3476-3486
[4]  
CLAESSONWELSH L, 1989, J BIOL CHEM, V264, P1742
[5]   MOLECULAR-CLONING OF GENE-SEQUENCES REGULATED BY PLATELET-DERIVED GROWTH-FACTOR [J].
COCHRAN, BH ;
REFFEL, AC ;
STILES, CD .
CELL, 1983, 33 (03) :939-947
[6]   FBJ MURINE OSTEO-SARCOMA VIRUS - IDENTIFICATION AND MOLECULAR-CLONING OF BIOLOGICALLY-ACTIVE PROVIRAL DNA [J].
CURRAN, T ;
PETERS, G ;
VANBEVEREN, C ;
TEICH, NM ;
VERMA, IM .
JOURNAL OF VIROLOGY, 1982, 44 (02) :674-682
[7]   P1B15 - A CDNA CLONE OF THE RAT MESSENGER-RNA ENCODING CYCLOPHILIN [J].
DANIELSON, PE ;
FORSSPETTER, S ;
BROW, MA ;
CALAVETTA, L ;
DOUGLASS, J ;
MILNER, RJ ;
SUTCLIFFE, JG .
DNA-A JOURNAL OF MOLECULAR & CELLULAR BIOLOGY, 1988, 7 (04) :261-267
[8]  
DROZDOFF V, 1991, J BIOL CHEM, V266, P17165
[9]   STIMULATION OF 3T3 CELLS INDUCES TRANSCRIPTION OF THE C-FOS PROTO-ONCOGENE [J].
GREENBERG, ME ;
ZIFF, EB .
NATURE, 1984, 311 (5985) :433-438
[10]  
HAMMACHER A, 1988, J BIOL CHEM, V263, P16493