Literature DB >> 6948604

Induction of differentiation of HL-60 cells by dimethyl sulfoxide: evidence for a stochastic model not linked to the cell division cycle.

C Tarella, D Ferrero, E Gallo, G L Pagliardi, F W Ruscetti.   

Abstract

Induction of differentiation of human promyelocytic leukemia cell line HL-60 by dimethyl sulfoxide (Me2SO) was analyzed to determine the relationship between exposure time of the inducer and cell cycle. A minimum incubation time of 12 hr with Me2SO was required in order to induce differentiation in a small but significant proportion of cells. These expressed differentiation markers (morphology, phagocytosis, and nitroblue tetrazolium reduction) up to 12 hr after Me2SO was removed from the medium. For periods beyond 12 hr and as long as 120 hr of contact of HL-60 cells with the inducing agent, a linear rise in the percentage of differentiated cells was observed. The sensitivity to Me2SO of HL-60 cells synchronized by double thymidine block was examined and was found to be similar to that of nonsynchronized cells. The effect of Me2SO was not altered when incubated with cells at different phases of the cell cycle. Finally, even nonproliferating cells were sensitive to the inducing effect of Me2SO. The data are consistent with a stochastic model of induction to differentiation without having any linkage to the cell cycle.

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Year:  1982        PMID: 6948604

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  22 in total

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4.  Two distinct mechanisms of transcriptional control operate on c-myc during differentiation of HL60 cells.

Authors:  U Siebenlist; P Bressler; K Kelly
Journal:  Mol Cell Biol       Date:  1988-02       Impact factor: 4.272

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7.  Influence of dimethyl sulphoxide on intermediate filament proteins in human rhabdomyosarcoma cell lines: modulation at subcellular level.

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8.  Cyclic nucleotide-induced maturation of human promyelocytic leukemia cells.

Authors:  T J Chaplinski; J E Niedel
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9.  In Vitro and In Vivo studies of monoclonal antibodies with prominent bactericidal activity against Burkholderia pseudomallei and Burkholderia mallei.

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Journal:  Cell Death Differ       Date:  2018-05-21       Impact factor: 15.828

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