Literature DB >> 6604639

Epidermal growth factor (EGF) is required only during the traverse of early G1 in PDGF stimulated density-arrested BALB/c-3T3 cells.

E B Leof, J J Van Wyk, E J O'Keefe, W J Pledger.   

Abstract

Density-arrested BALB/c-3T3 cells that had received a transient exposure to PDGF and were then transferred to medium containing only EGF and somatomedin C (Sm-C) began DNA synthesis after the G0/G1 lag. Supraphysiological concentrations of insulin could be employed to replace the Sm-C requirement. This G0/G1 lag phase was bisected by the requirement for the exogenous presence of EGF. Our data indicated that EGF was required during the traverse of only the first half of G0/G1 phase (6 h) and not during the traverse of late G1. Subphysiological serum concentrations of Sm-C were also necessary to be present with EGF for progression through early G0/G1; however, traverse of the final half of G0/G1 and commitment to DNA synthesis required the presence of Sm-C. It was found that physiological concentrations of Sm-C were required for the traverse late G1. The requirement for Sm-C for G0/G1 traverse of BALB/c-3T3 cells as opposed to human fibroblasts or glial cells may be due to a difference in endogenous synthesis of an insulin-like growth factor. Our data are in close agreement with previous reports that EGF is only required for approximately the first 8 h during traverse of the G0/G1 phase. The requirement for EGF to be present for the first 6 h of G0/G1 could result from a continued or repetitious event or by more than one distinct EGF-requiring event.

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Year:  1983        PMID: 6604639     DOI: 10.1016/0014-4827(83)90285-9

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  25 in total

1.  p27Kip1 inhibits the cell cycle through non-canonical G1/S phase-specific gatekeeper mechanism.

Authors:  Savitha S Sharma; Le Ma; W Jackson Pledger
Journal:  Cell Cycle       Date:  2015       Impact factor: 4.534

2.  Stabilized complexes of epidermal growth factor and its receptor on the cell surface stimulate RNA synthesis but not mitogenesis.

Authors:  E M Wakshull; W Wharton
Journal:  Proc Natl Acad Sci U S A       Date:  1985-12       Impact factor: 11.205

3.  Ras proteins are essential and selective for the action of insulin-like growth factor 1 late in the G1 phase of the cell cycle in BALB/c murine fibroblasts.

Authors:  K Lu; J Campisi
Journal:  Proc Natl Acad Sci U S A       Date:  1992-05-01       Impact factor: 11.205

4.  The platelet-derived growth factor alpha-receptor is encoded by a growth-arrest-specific (gas) gene.

Authors:  C J Lih; S N Cohen; C Wang; S Lin-Chao
Journal:  Proc Natl Acad Sci U S A       Date:  1996-05-14       Impact factor: 11.205

5.  Identification of an autocrine mechanism for regulating cell-cycle progression in murine keratinocytes.

Authors:  G M Curtin; S M Fischer; T J Slaga
Journal:  J Cancer Res Clin Oncol       Date:  1997       Impact factor: 4.553

6.  Growth factors in wound healing. Single and synergistic effects on partial thickness porcine skin wounds.

Authors:  S E Lynch; R B Colvin; H N Antoniades
Journal:  J Clin Invest       Date:  1989-08       Impact factor: 14.808

7.  c-ras-Ha gene expression is regulated by insulin or insulinlike growth factor and by epidermal growth factor in murine fibroblasts.

Authors:  K H Lu; R A Levine; J Campisi
Journal:  Mol Cell Biol       Date:  1989-08       Impact factor: 4.272

8.  Vitamin A in serum is a survival factor for fibroblasts.

Authors:  Y Chen; F Derguini; J Buck
Journal:  Proc Natl Acad Sci U S A       Date:  1997-09-16       Impact factor: 11.205

9.  Recombinants within the tyrosine kinase region of v-abl and v-src identify a v-abl segment that confers lymphoid specificity.

Authors:  B Mathey-Prevot; D Baltimore
Journal:  Mol Cell Biol       Date:  1988-01       Impact factor: 4.272

Review 10.  Hair cell regeneration in the bird cochlea following noise damage or ototoxic drug damage.

Authors:  D A Cotanche; K H Lee; J S Stone; D A Picard
Journal:  Anat Embryol (Berl)       Date:  1994-01
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