Literature DB >> 2077941

Isolation of cell cycle fractions by counterflow centrifugal elutriation.

M G Kauffman1, S J Noga, T J Kelly, A D Donnenberg.   

Abstract

Counterflow centrifugal elutriation (CCE) has been used to fractionate cell populations on the basis of sedimentation properties, with minimal perturbation of metabolic function. Therefore, it is an ideal method for the isolation of cell cycle phase specific populations. We present modifications of the standard Beckman centrifugal elutriation system which permit standardization of the elutriation procedure and eliminate inter-run variability. We provide elutriation parameters for the cell cycle fractionation of a variety of cultured cell lines and suggest ways to improve the quality of the cell separations. In addition, we describe protocols for the fractionation of up to 3.50 X 10(8) cells in the small (JE-6B) Beckman elutriation system. This represents a four- to eight-fold increase in cell numbers over current cell fractionation procedures. Cell cycle populations containing greater than 95% G1, greater than 80% S, and greater than 70% G2/M were consistently obtained using these protocols. Finally, we analyzed phase-enriched fractions from several cultured cell lines for the cell cycle regulation of the enzyme thymidine kinase. The data confirm previous findings that CCE is an excellent means of obtaining physiologically unperturbed cell cycle phase specific fractions.

Entities:  

Mesh:

Year:  1990        PMID: 2077941     DOI: 10.1016/0003-2697(90)90384-l

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  10 in total

1.  Cell cycle regulation of thymidine kinase: residues near the carboxyl terminus are essential for the specific degradation of the enzyme at mitosis.

Authors:  M G Kauffman; T J Kelly
Journal:  Mol Cell Biol       Date:  1991-05       Impact factor: 4.272

2.  The p110 isoform of the CDP/Cux transcription factor accelerates entry into S phase.

Authors:  Laurent Sansregret; Brigitte Goulet; Ryoko Harada; Brian Wilson; Lam Leduy; Jacques Bertoglio; Alain Nepveu
Journal:  Mol Cell Biol       Date:  2006-03       Impact factor: 4.272

3.  A UV-responsive G2 checkpoint in rodent cells.

Authors:  D K Orren; L N Petersen; V A Bohr
Journal:  Mol Cell Biol       Date:  1995-07       Impact factor: 4.272

4.  Characterization of ATM expression, localization, and associated DNA-dependent protein kinase activity.

Authors:  D P Gately; J C Hittle; G K Chan; T J Yen
Journal:  Mol Biol Cell       Date:  1998-09       Impact factor: 4.138

5.  Merging high-quality biochemical fractionation with a refined flow cytometry approach to monitor nucleocytoplasmic protein expression throughout the unperturbed mammalian cell cycle.

Authors:  Margit Rosner; Katharina Schipany; Markus Hengstschläger
Journal:  Nat Protoc       Date:  2013-02-28       Impact factor: 13.491

6.  Regulation of cyclin D1, DNA topoisomerase I, and proliferating cell nuclear antigen promoters during the cell cycle.

Authors:  H H Lee; W H Chiang; S H Chiang; Y C Liu; J Hwang; S Y Ng
Journal:  Gene Expr       Date:  1995

7.  Growth factor-induced delayed early response genes.

Authors:  A Lanahan; J B Williams; L K Sanders; D Nathans
Journal:  Mol Cell Biol       Date:  1992-09       Impact factor: 4.272

8.  An intranucleolar body associated with rDNA.

Authors:  Saskia Hutten; Alan Prescott; John James; Stefanie Riesenberg; Séverine Boulon; Yun Wah Lam; Angus I Lamond
Journal:  Chromosoma       Date:  2011-06-23       Impact factor: 4.316

9.  Calcium Imaging of GPCR Activation Using Arrays of Reverse Transfected HEK293 Cells in a Microfluidic System.

Authors:  Margriet Roelse; Maurice G L Henquet; Harrie A Verhoeven; Norbert C A de Ruijter; Ron Wehrens; Marco S van Lenthe; Renger F Witkamp; Robert D Hall; Maarten A Jongsma
Journal:  Sensors (Basel)       Date:  2018-02-16       Impact factor: 3.576

10.  Cyclin-like accumulation and loss of the putative kinetochore motor CENP-E results from coupling continuous synthesis with specific degradation at the end of mitosis.

Authors:  K D Brown; R M Coulson; T J Yen; D W Cleveland
Journal:  J Cell Biol       Date:  1994-06       Impact factor: 10.539

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.