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pubmed-article:1400610pubmed:abstractTextPlatelet-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.lld:pubmed
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pubmed-article:1400610pubmed:dateRevised2009-11-19lld:pubmed
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pubmed-article:1400610pubmed:articleTitleRapid induction of competence formation is PDGF-isoform specific.lld:pubmed
pubmed-article:1400610pubmed:affiliationDepartment of Cell Biology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232.lld:pubmed
pubmed-article:1400610pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1400610pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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