Literature DB >> 15534858

Changes in cell shape and anchorage in relation to the restriction point.

Hanna-Stina Martinsson1, Peter Zickert, Maria Starborg, Olle Larsson, Anders Zetterberg.   

Abstract

The restriction point (R) separates the G1 phase of continuously cycling cells into two functionally different parts. The first part, G1-pm, represents the growth factor dependent post-mitotic interval from mitosis to R, which is of constant length (3-4 h). The second part, G1-ps, represents the growth factor independent, pre-S phase interval of G1 that lasts from R to S and that varies in time from 1 to 10 h. G1-pm cells rapidly exit (within 1 h) from the cell cycle and enter G0 as a response to serum withdrawal. The finding that R occurs at a set time after mitosis indicates that R may be related to the metabolic and/or structural changes that the cell underwent during the previous mitosis. We have recently shown that phosphorylation of the retinoblastoma tumor suppressor protein (pRb) is not the molecular mechanism behind R, as has been suggested previously. Here, we present an alternative explanation for R. In the present study, we applied a single cell approach using time-lapse analysis, which revealed that upon serum starvation the G1-pm cells rapidly underwent a transient change in cell shape from flat to spherical before exiting to G0. Platelet derived growth factor (PDGF) counteracted this change in shape and also prevented exit to G0 to the same extent. Furthermore epidermal growth factor (EGF) and insulin like growth factor (IGF-1), which only partially counteracted this change, only partially counteracts exit to G0. These data clearly indicate a direct link between change in cell shape and exit to G0 in G1-cells that have not passed R. 2004 Wiley-Liss, Inc.

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Year:  2005        PMID: 15534858     DOI: 10.1002/jcp.20204

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


  2 in total

1.  Cell Cycle and Cell Size Dependent Gene Expression Reveals Distinct Subpopulations at Single-Cell Level.

Authors:  Soheila Dolatabadi; Julián Candia; Nina Akrap; Christoffer Vannas; Tajana Tesan Tomic; Wolfgang Losert; Göran Landberg; Pierre Åman; Anders Ståhlberg
Journal:  Front Genet       Date:  2017-01-25       Impact factor: 4.599

2.  Regulation of cell cycle entry by PTEN in smooth muscle cell proliferation of human coronary artery bypass conduits.

Authors:  Guanghong Jia; Amit K Mitra; Deepak M Gangahar; Devendra K Agrawal
Journal:  J Cell Mol Med       Date:  2009-03       Impact factor: 5.310

  2 in total

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