Literature DB >> 1462732

Measurement of efflux from G1-phase in a growth factor dependent cell line.

J W Ellwart1, P Dörmer.   

Abstract

In order to test a mathematical model of G1/S-phase transition, the proliferative response of the murine myeloid interleukin 3 (IL-3) dependent cell line NFS-78 to graded reduction of IL-3 levels was measured. Exponentially growing cells were exposed to bromodeoxyuridine (BUdR), which replaces thymidine (TdR) in the DNA double strands during DNA synthesis. After incubation periods ranging from 3 to 36 h the cells were fixed and stained with a fluorescence dye mixture of Hoechst 33258 and ethidium bromide (EB) and subsequently analyzed in a two-parametrical flow cytometer. The BUdR-quenched TdR-specific Hoechst 33258 fluorescence of each cell provides information on the cell cycle location at the start of incubation and on whether or not a cell has divided. The DNA-specific EB fluorescence provides information on the actual cell cycle location at the end of the incubation period. From the 2-dimensional fluorescence distributions the efflux from G1-phase was calculated. Upon IL-3 reduction the cells showed accumulation in the G1-phase along with a reduction in the progression rate through the other phases of the cell cycle. By staining with the vital dye Hoechst 33342 as well as with propidium iodide (PI) it was further possible to show that cell death after IL-3 withdrawal occurred in all phases of the cell cycle.

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Year:  1992        PMID: 1462732     DOI: 10.1007/bf00168143

Source DB:  PubMed          Journal:  Acta Biotheor        ISSN: 0001-5342            Impact factor:   1.774


  13 in total

1.  Vitality measurement using spectrum shift in Hoechst 33342 stained cells.

Authors:  J W Ellwart; P Dörmer
Journal:  Cytometry       Date:  1990

2.  Interleukin 3 and cell cycle progression.

Authors:  D J Kelvin; S Chance; M Shreeve; A A Axelrad; J A Connolly; D McLeod
Journal:  J Cell Physiol       Date:  1986-06       Impact factor: 6.384

3.  Rate of DNA synthesis determined by flow cytometry using the BrdUrd/Hoechst technique in combination with propidium-iodide staining.

Authors:  J Ellwart; R M Böhmer; P Dörmer
Journal:  Exp Cell Res       Date:  1982-05       Impact factor: 3.905

4.  Colony-stimulating factor (CSF) controls proliferation of CSF-dependent cells by acting during the G1 phase of the cell cycle.

Authors:  D H Pluznik; R E Cunningham; P D Noguchi
Journal:  Proc Natl Acad Sci U S A       Date:  1984-12       Impact factor: 11.205

5.  Application of the CYTOMIC 12 flow cytometric compact analyzer for automatic kinetic measurements.

Authors:  V Kachel; H Schneider; J Bauer; J Malin-Berdel
Journal:  Cytometry       Date:  1983-01

6.  Cell cycle analysis by combining the 5-bromodeoxyuridine/33258 Hoechst technique with DNA-specific ethidium bromide staining.

Authors:  R M Böhmer; J Ellwart
Journal:  Cytometry       Date:  1981-07

7.  Combination of BUdR-quenched Hoechst fluorescence with DNA-specific ethidium bromide fluorescence for cell cycle analysis with a two-parameter flow cytometer.

Authors:  R M Böhmer; J Ellwart
Journal:  Cell Tissue Kinet       Date:  1981-11

8.  Procedures for the purification of interleukin 3 to homogeneity.

Authors:  J N Ihle; J Keller; L Henderson; F Klein; E Palaszynski
Journal:  J Immunol       Date:  1982-12       Impact factor: 5.422

9.  Correlation of cell-surface phenotype with the establishment of interleukin 3-dependent cell lines from wild-mouse murine leukemia virus-induced neoplasms.

Authors:  K L Holmes; E Palaszynski; T N Fredrickson; H C Morse; J N Ihle
Journal:  Proc Natl Acad Sci U S A       Date:  1985-10       Impact factor: 11.205

10.  Activation and growth of colony-stimulating factor-dependent cell lines is cell cycle stage dependent.

Authors:  L London; J P McKearn
Journal:  J Exp Med       Date:  1987-11-01       Impact factor: 14.307

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