Experimental reconsideration of the utility of serum starvation as a method for synchronizing mammalian cells
dc.contributor.author | Cooper, Stephen | en_US |
dc.contributor.author | Gonzalez‐hernandez, Mariam | en_US |
dc.date.accessioned | 2013-02-12T19:00:17Z | |
dc.date.available | 2013-02-12T19:00:17Z | |
dc.date.issued | 2009-01 | en_US |
dc.identifier.citation | Cooper, Stephen; Gonzalez‐hernandez, Mariam (2009). "Experimental reconsideration of the utility of serum starvation as a method for synchronizing mammalian cells." Cell Biology International 33(1). <http://hdl.handle.net/2027.42/96238> | en_US |
dc.identifier.issn | 1065-6995 | en_US |
dc.identifier.issn | 1095-8355 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/96238 | |
dc.description.abstract | Accurate cell‐size determinations support the prediction that serum starvation and related whole‐culture methods cannot synchronize cells. Theoretical considerations predict that whole‐culture methods of synchronization cannot synchronize cells. Upon serum starvation, the fraction of cells with a G1‐phase amount of DNA increased, but the cell‐size distribution is not narrowed. In true synchronization, the cell‐size distribution should be narrower than the cell‐size distribution of the original culture. In contrast, cells produced by a selective (i.e. non‐whole‐culture) method have a specific DNA content, a narrow size distribution, and divide synchronously. The general theory leading to the conclusion that whole‐culture methods for synchronization do not work implies that one can generalize these serum‐starvation results to other cell lines and other whole‐culture methods, to conclude that these methods do not synchronize cells. | en_US |
dc.publisher | Blackwell Publishing Ltd | en_US |
dc.publisher | Wiley Periodicals, Inc. | en_US |
dc.subject.other | G1 Phase | en_US |
dc.subject.other | Serum Starvation | en_US |
dc.subject.other | Membrane Elution | en_US |
dc.subject.other | Synchronization | en_US |
dc.subject.other | Cell Cycle | en_US |
dc.title | Experimental reconsideration of the utility of serum starvation as a method for synchronizing mammalian cells | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Molecular, Cellular and Developmental Biology | en_US |
dc.subject.hlbtoplevel | Science | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109‐0620, USA | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/96238/1/j.cellbi.2008.09.009.pdf | |
dc.identifier.doi | 10.1016/j.cellbi.2008.09.009 | en_US |
dc.identifier.source | Cell Biology International | en_US |
dc.identifier.citedreference | Keyomarsi K. Sandoval L. Band V. Pardee A.B. Synchronization of tumor and normal cells from G1 to multiple cell cycles by lovastatin Cancer Res 51 1991 3602 – 3609. | en_US |
dc.identifier.citedreference | Cooper S. Shedden K. Microarray analysis of gene expression during the cell cycle Cell Chromosome 2 2003 1 – 12. | en_US |
dc.identifier.citedreference | Cooper S. Iyer G. Tarquini M. Bissett P. Nocodazole does not synchronize cells: implications for cell‐cycle control and whole‐culture synchronization Cell Tissue Res 324 2006 237 – 242. | en_US |
dc.identifier.citedreference | Cooper S. Chen K.Z. Ravi S. Thymidine block does not synchronize L1210 mouse leukaemic cells: implications for cell cycle control, cell cycle analysis and whole‐culture synchronization Cell Prolif 41 2008 156 – 167. | en_US |
dc.identifier.citedreference | Davis P.K. Ho A. Dowdy S.F. Biological methods for cell‐cycle synchronization of mammalian cells Biotechniques 30 2001 1322 – 1326 1328, 1330‐31. | en_US |
dc.identifier.citedreference | Di Matteo G. Fuschi P. Zerfass K. Moretti S. Ricordy R. Cenciarelli C. Tripodi M. Jansen‐Durr P. Lavia P. Transcriptional control of the Htf9‐A/RanBP‐1 gene during the cell cycle Cell Growth Differ 6 1995 1213 – 1224. | en_US |
dc.identifier.citedreference | Eward K.L. Van Ert M.N. Thornton M. Helmstetter C.E. Cyclin mRNA stability does not vary during the cell cycle Cell Cycle 3 2004 1057 – 1061. | en_US |
dc.identifier.citedreference | Gong J. Traganos F. Darzynkiewicz Z. 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 Cell Growth Differ 6 1995 1485 – 1493. | en_US |
dc.identifier.citedreference | Harper J.V. Synchronization of cell populations in G1/S and G2/M phases of the cell cycle Methods Mol Biol 296 2005 157 – 166. | en_US |
dc.identifier.citedreference | Helmstetter C. Cooper S. Pierucci O. Revelas E. On the bacterial life sequence Cold Spring Harb Symp Quant Biol 33 1968 809 – 822. | en_US |
dc.identifier.citedreference | Helmstetter C.E. Thornton M. Romero A. Eward K.L. Synchrony in human, mouse and bacterial cell cultures – a comparison Cell Cycle 2 2003 42 – 45. | en_US |
dc.identifier.citedreference | Jansen‐Durr P. Meichle A. Steiner P. Pagano M. Finke K. Botz J. Wessbecher J. Draetta G. Eilers M. Differential modulation of cyclin gene expression by MYC Proc Natl Acad Sci U S A 90 1993 3685 – 3689. | en_US |
dc.identifier.citedreference | Kung A.L. Sherwood S.W. Schimke R.T. Cell line‐specific differences in the control of cell cycle progression in the absence of mitosis Proc Natl Acad Sci U S A 87 1990 9553 – 9557. | en_US |
dc.identifier.citedreference | Laoukili J. Alvarez M. Meijer L.A. Stahl M. Mohammed S. Kleij L. Heck A.J. Medema R.H. Activation of FoxM1 during G2 requires cyclin A/Cdk‐dependent relief of autorepression by the FoxM1 N‐terminal domain Mol Cell Biol 28 2008 3076 – 3087. | en_US |
dc.identifier.citedreference | Le Francois B.G. Maroun J.A. Birnboim H.C. Expression of thymidylate synthase in human cells is an early G(1) event regulated by CDK4 and p16INK4A but not E2F Br J Cancer 97 2007 1242 – 1250. | en_US |
dc.identifier.citedreference | Liliensiek S.J. Schell K. Howard E. Nealey P. Murphy C.J. Cell sorting but not serum starvation is effective for SV40 human corneal epithelial cell cycle synchronization Exp Eye Res 83 2006 61 – 68. | en_US |
dc.identifier.citedreference | Ludlow J.W. Glendening C.L. Livingston D.M. DeCaprio J.A. Specific enzymatic dephosphorylation of the retinoblastoma protein Mol Cell Biol 13 1993 367 – 372. | en_US |
dc.identifier.citedreference | Ouyang B. Lan Z. Meadows J. Pan H. Fukasawa K. Li W. Dai W. Human Bub1: a putative spindle checkpoint kinase closely linked to cell proliferation Cell Growth Differ 9 1998 877 – 885. | en_US |
dc.identifier.citedreference | Pardee A.B. A restriction point for control of normal animal cell proliferation Proc Natl Acad Sci U S A 71 1974 1286 – 1290. | en_US |
dc.identifier.citedreference | Shedden K. Cooper S. Analysis of cell‐cycle‐specific gene expression in human cells as determined by microarrays and double‐thymidine block synchronization Proc Natl Acad Sci U S A 99 2002 4379 – 4384. | en_US |
dc.identifier.citedreference | Shedden K. Cooper S. Analysis of cell‐cycle‐specific gene expression in Saccharomyces cerevisiae as determined by Microarrays and Multiple synchronization methods Nucleic Acids Res 30 2002 2920 – 2929. | en_US |
dc.identifier.citedreference | Thornton M. Eward K.L. Helmstetter C.E. Production of minimally disturbed synchronous cultures of hematopoietic cells Biotechniques 32 2002 1098 – 1105. | en_US |
dc.identifier.citedreference | Bar‐Joseph Z. Siegfried Z. Brandeis M. Brors B. Lu Y. Eils R. Dynlacht B.D. Simon I. Genome‐wide transcriptional analysis of the human cell cycle identifies genes differentially regulated in normal and cancer cells Proc Natl Acad Sci U S A 105 2008 955 – 960. | en_US |
dc.identifier.citedreference | Cho R.J. Huang M. Campbell M.J. Dong H. Steinmetz L. Sapinoso L. Hampton G. Elledge S.J. Davis R.W. Lockhart D.J. Transcriptional regulation and function during the human cell cycle Nat Genet 27 2001 48 – 54. | en_US |
dc.identifier.citedreference | Cooper S. A unifying model for the G1 period in prokaryotes and eukaryotes Nature 280 1979 17 – 19. | en_US |
dc.identifier.citedreference | Cooper S. Bacterial growth and division 1991 Academic Press San Diego, CA. | en_US |
dc.identifier.citedreference | Cooper S. Length extension in growing yeast: is growth exponential? – yes Microbiology 144 1998 263 – 265. | en_US |
dc.identifier.citedreference | Cooper S. Mammalian cells are not synchronized in G1‐phase by starvation or inhibition: considerations of the fundamental concept of G1‐phase synchronization Cell Prolif 31 1998 9 – 16. | en_US |
dc.identifier.citedreference | Cooper S. Reappraisal of G1‐phase arrest and synchronization by lovastatin Cell Biol Int 26 2002 715 – 727. | en_US |
dc.identifier.citedreference | Cooper S. How the change from FLM to FACS affected our understanding of the G1 phase of the cell cycle Cell Cycle 2 2003 157 – 159. | en_US |
dc.identifier.citedreference | Cooper S. Rethinking synchronization of mammalian cells for cell‐cycle analysis Cell Mol Life Sci 6 2003 1099 – 1106. | en_US |
dc.identifier.citedreference | Cooper S. Reappraisal of serum starvation, the restriction point, G0, and G1‐phase arrest points FASEB J 17 2003 333 – 340. | en_US |
dc.identifier.citedreference | Cooper S. Is whole‐culture synchronization biology's ‘Perpetual Motion Machine’? Trends Biotechnol 26 2004 266 – 269. | en_US |
dc.identifier.citedreference | Cooper S. Rejoinder: whole‐culture synchronization cannot, and does not, synchronize cells Trends Biotechnol 22 2004 274 – 276. | en_US |
dc.identifier.citedreference | Cooper S. Whole‐culture synchronization cannot, and does not, synchronize cells Trends Biotechnol 22 2004 274 – 276. | en_US |
dc.identifier.citedreference | Cooper S. Bacterial and eukaryotic checkpoints and restriction points Bioessays 28 2006 1035 – 1039. | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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