Literature DB >> 12861378

Rethinking synchronization of mammalian cells for cell cycle analysis.

S Cooper1.   

Abstract

An analysis of different classes of forced or batch synchronization methods reveals why these methods, in theory, do not produce synchronized cultures. Cells may be aligned for a particular property after specific treatments, but these aligned cells do not correspond to any particular cell age during the normal cell cycle. The experimental methods analyzed are those that arrest cells with a G1 phase amount of DNA, those that inhibit DNA synthesis, and those that arrest cells at mitosis. Release of arrested cells from inhibition does not produce cells reflecting cells during the normal division cycle. Thus, cells produced by batch or forcing methods are not experimental models for analysis of the normal cell cycle.

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Year:  2003        PMID: 12861378     DOI: 10.1007/s00018-003-2253-2

Source DB:  PubMed          Journal:  Cell Mol Life Sci        ISSN: 1420-682X            Impact factor:   9.261


  36 in total

1.  Ion channels in volume regulation of clonal kidney cells.

Authors:  M B da Silva; V M A Costa; V R A Pereira; G J B de Albertim; E B B de Melo; D P Bezerra; R P da Silva; C G Rodrigues; C M M Carneiro; L N Yuldasheva; O V Krasilnikov
Journal:  Cell Prolif       Date:  2010-12       Impact factor: 6.831

2.  Cell sorting but not serum starvation is effective for SV40 human corneal epithelial cell cycle synchronization.

Authors:  Sara J Liliensiek; Kathleen Schell; Elise Howard; Paul Nealey; Christopher J Murphy
Journal:  Exp Eye Res       Date:  2006-03-20       Impact factor: 3.467

3.  Identifying genes involved in cyclic processes by combining gene expression analysis and prior knowledge.

Authors:  Wentao Zhao; Erchin Serpedin; Edward R Dougherty
Journal:  EURASIP J Bioinform Syst Biol       Date:  2009-04-15

4.  Detecting periodic genes from irregularly sampled gene expressions: a comparison study.

Authors:  Wentao Zhao; Kwadwo Agyepong; Erchin Serpedin; Edward R Dougherty
Journal:  EURASIP J Bioinform Syst Biol       Date:  2008

5.  Development of pharmacodynamic biomarkers for ATR inhibitors.

Authors:  Tao Chen; Fiona K Middleton; Susanna Falcon; Philip M Reaper; John R Pollard; Nicola J Curtin
Journal:  Mol Oncol       Date:  2014-10-13       Impact factor: 6.603

6.  Patterns of Early p21 Dynamics Determine Proliferation-Senescence Cell Fate after Chemotherapy.

Authors:  Chien-Hsiang Hsu; Steven J Altschuler; Lani F Wu
Journal:  Cell       Date:  2019-06-13       Impact factor: 41.582

7.  Combining Mitotic Cell Synchronization and High Resolution Confocal Microscopy to Study the Role of Multifunctional Cell Cycle Proteins During Mitosis.

Authors:  Mohammed A Amin; Dileep Varma
Journal:  J Vis Exp       Date:  2017-12-05       Impact factor: 1.355

8.  Quantification of cellular and nuclear uptake rates of polymeric gene delivery nanoparticles and DNA plasmids via flow cytometry.

Authors:  Corey J Bishop; Rebecca L Majewski; Toni-Rose M Guiriba; David R Wilson; Nupura S Bhise; Alfredo Quiñones-Hinojosa; Jordan J Green
Journal:  Acta Biomater       Date:  2016-03-24       Impact factor: 8.947

9.  Polyplex exposure inhibits cell cycle, increases inflammatory response, and can cause protein expression without cell division.

Authors:  Rebecca L Matz; Blake Erickson; Sriram Vaidyanathan; Jolanta F Kukowska-Latallo; James R Baker; Bradford G Orr; Mark M Banaszak Holl
Journal:  Mol Pharm       Date:  2013-03-21       Impact factor: 4.939

10.  Thymidine block does not synchronize L1210 mouse leukaemic cells: implications for cell cycle control, cell cycle analysis and whole-culture synchronization.

Authors:  S Cooper; K Z Chen; S Ravi
Journal:  Cell Prolif       Date:  2008-02       Impact factor: 6.831

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