Literature DB >> 6163546

Reversible (G0) and nonreadily reversible (Q) noncycling cells in human peripheral blood. Immunological, structural, and biological characterization.

S Abraham, E Vonderheid, S Zietz, F M Kendall, C Nicolini.   

Abstract

PHA-stimulated human lymphocytes (normal-resting-proliferating) at 0, 24, 48, 72, and 144 h were studied with Acridine Orange (AO) staining. By viable cell sorting, by subsequent subculturing, and by the use of biochemical, biophysical, and immunological assays, not only have the G0 resting and G1 (cycling) cell cycle phases been objectively characterized, but a separate subpopulation of quiescent cells that are functionally viable and deeply committed to nonproliferation, the Q cells, has been identified. Multiparameter cytofluorimetric analysis, methyl14C-thymidine incorporation, automated image analysis, and mitogen stimulation studies have shown that the "Q" cell, compared to the "G0" resting but easily recruitable cell, exhibits quite lower red and green AO emission, possesses 2c to 4c DNA content (rather than only 2c), has a higher average optical density, and is either nonrecruitable or recruitable-with-difficulty in PHA-stimulated lymphocyte cultures.

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Year:  1980        PMID: 6163546     DOI: 10.1007/BF02785099

Source DB:  PubMed          Journal:  Cell Biophys        ISSN: 0163-4992


  11 in total

1.  The use of fluorescamine as a probe for labeling the outer surface of the plasma membrane.

Authors:  S P Hawkes; T D Meehan; M J Bissell
Journal:  Biochem Biophys Res Commun       Date:  1976-02-23       Impact factor: 3.575

2.  Use of baker's yeast to detect complement receptor.

Authors:  S G Barrett
Journal:  Blood       Date:  1978-04       Impact factor: 22.113

3.  Morphogenesis in blood lymphocytes stimulated with phytohaemagglutinin (PHA). A light and electron microscopic study.

Authors:  P Biberfeld
Journal:  Acta Pathol Microbiol Scand Suppl       Date:  1971

4.  Studies of template activity of chromatin isolated from metabolically active and inactive cells.

Authors:  V Seligy; M Miyagi
Journal:  Exp Cell Res       Date:  1969-11       Impact factor: 3.905

Review 5.  Normal versus abnormal cell proliferation. A unitary and analytical overview.

Authors:  C Nicolini
Journal:  Cell Biophys       Date:  1980-12

6.  Mass action and acridine orange staining: static and flow cytofluorometry.

Authors:  C Nicolini; A Belmont; S Parodi; S Lessin; S Abraham
Journal:  J Histochem Cytochem       Date:  1979-01       Impact factor: 2.479

7.  The G0-G1 transition of WI38 cells. I. Laser flow microfluorimetric studies.

Authors:  C Nicolini; F Kendall; R Baserga; C Dessaive; B Clarkson; J Fried
Journal:  Exp Cell Res       Date:  1977-04       Impact factor: 3.905

8.  Identification of non-proliferating cells in melanoma B16 tumour.

Authors:  C A Nicolini; W A Linden; S Zietz; C T Wu
Journal:  Nature       Date:  1977-12-15       Impact factor: 49.962

9.  Discrete changes of the fluorescence yield from cells vitally stained with ethidium bromide (EB), as determined by flow cytometry.

Authors:  R M Böhmer
Journal:  Exp Cell Res       Date:  1979-09       Impact factor: 3.905

10.  Physical-chemical characterization of living cells by laser-flow microfluorometry.

Authors:  C Nicolini; F Kendall; C Desaive; R Baserga; B Clarkson; J Fried
Journal:  Cancer Treat Rep       Date:  1976-12
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  2 in total

Review 1.  Normal versus abnormal cell proliferation. A unitary and analytical overview.

Authors:  C Nicolini
Journal:  Cell Biophys       Date:  1980-12

2.  The G1 period. Two cycles of chromatin conformational changes monitored by single cell dye intercalation.

Authors:  A Belmont; C Nicolini
Journal:  Cell Biophys       Date:  1983-06
  2 in total

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