Literature DB >> 19002885

Technology for cell cycle research with unstressed steady-state cultures.

Valerie S Lebleu1, Maureen Thornton, Steven R Gonda, Charles E Helmstetter.   

Abstract

A culture system for performing cell cycle analyses on cells in undisturbed steady-state populations was designed and tested. In this system, newborn cells are shed continuously from an immobilized, perfused culture rotating about the horizontal axis. As a result of this arrangement, the number of newborn cells released into the effluent medium each generation is identical to the number of cells residing in the immobilized population, indicating that one of the two new daughter cells is shed at each cell division. Thus, the immobilized cells constitute a continuous, steady-state culture because the concentrations, locations and microenvironments of the cells in the culture vessel do not vary with time. In tests with mouse L1210 lymphocytic leukemia cells, about 10(8) newborn cells were produced per day. This new culture system enables a multiplicity of cell cycle analyses on large numbers of cells assured to be from populations in steady-state growth.

Entities:  

Year:  2006        PMID: 19002885      PMCID: PMC3449808          DOI: 10.1007/s10616-006-9024-5

Source DB:  PubMed          Journal:  Cytotechnology        ISSN: 0920-9069            Impact factor:   2.058


  19 in total

Review 1.  Biological methods for cell-cycle synchronization of mammalian cells.

Authors:  P K Davis; A Ho; S F Dowdy
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2.  Synchronous cultures from the baby machine. A model for animal cells.

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Authors:  C E Helmstetter
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Review 4.  Cell synchronization.

Authors:  G F Merrill
Journal:  Methods Cell Biol       Date:  1998       Impact factor: 1.441

5.  Gravity and the orientation of cell division.

Authors:  C E Helmstetter
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6.  Cyclin mRNA stability does not vary during the cell cycle.

Authors:  K Leigh Eward; Matthew N Van Ert; Maureen Thornton; Charles E Helmstetter
Journal:  Cell Cycle       Date:  2004-08-17       Impact factor: 4.534

7.  Growth imbalance and altered expression of cyclins B1, A, E, and D3 in MOLT-4 cells synchronized in the cell cycle by inhibitors of DNA replication.

Authors:  J Gong; F Traganos; Z Darzynkiewicz
Journal:  Cell Growth Differ       Date:  1995-11

8.  Mammalian cells are not synchronized in G1-phase by starvation or inhibition: considerations of the fundamental concept of G1-phase synchronization.

Authors:  S Cooper
Journal:  Cell Prolif       Date:  1998-02       Impact factor: 6.831

9.  Dissociation of nuclear and cytoplasmic cell cycle progression by drugs employed in cell synchronization.

Authors:  L Urbani; S W Sherwood; R T Schimke
Journal:  Exp Cell Res       Date:  1995-07       Impact factor: 3.905

10.  DNA replication licensing in somatic and germ cells.

Authors:  Kathryn Leigh Eward; Ellen C Obermann; S Shreeram; Marco Loddo; Thomas Fanshawe; Craig Williams; Hyo-Il Jung; A Toby Prevost; J Julian Blow; Kai Stoeber; Gareth H Williams
Journal:  J Cell Sci       Date:  2004-11-02       Impact factor: 5.285

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  4 in total

1.  Cell growth and size homeostasis in proliferating animal cells.

Authors:  Amit Tzur; Ran Kafri; Valerie S LeBleu; Galit Lahav; Marc W Kirschner
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2.  Using standard optical flow cytometry for synchronizing proliferating cells in the G1 phase.

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Journal:  PLoS One       Date:  2013-12-31       Impact factor: 3.240

3.  Membrane-elution analysis of content of cyclins A, B1, and E during the unperturbed mammalian cell cycle.

Authors:  Stephen Cooper; Michelle Paulsen; Mats Ljungman; Dang Vu-Phan; Duyang Kim; Mariam Gonzalez-Hernandez
Journal:  Cell Div       Date:  2007-09-24       Impact factor: 5.130

4.  Purifying Cytokinetic Cells from an Asynchronous Population.

Authors:  Einat Panet; Efrat Ozer; Tal Mashriki; Itay Lazar; Devora Itzkovich; Amit Tzur
Journal:  Sci Rep       Date:  2015-08-11       Impact factor: 4.379

  4 in total

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