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Isoenzymes of lactate dehydrogenase in human leukemic cells in culture treated with inducers of differentiation

The human leukemic cell lines HL60 and K562, were induced to differentiate terminally by chemical agents. The isoenzyme patterns of lactate dehydrogenase (LD) in the cells before and after differentiation were determined electrophoretically on agarose gels. In general, treatment of the leukemic cell...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1981
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2111856/
https://www.ncbi.nlm.nih.gov/pubmed/6945307
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collection PubMed
description The human leukemic cell lines HL60 and K562, were induced to differentiate terminally by chemical agents. The isoenzyme patterns of lactate dehydrogenase (LD) in the cells before and after differentiation were determined electrophoretically on agarose gels. In general, treatment of the leukemic cells with inducers of differentiation resulted in a quantitative shift of the isoenzyme pattern towards anodic or cathodic forms. This was correlated with the conversion of the chemically treated cells to morphologically more normal cells, as verified by light microscopy and/or synthesis of hemoglobin. The LD isoenzyme patterns of the chemically differentiated cells were: (a) characteristic for the particular cell type obtained rather than for the nature of the inducer used; and (b) not similar to those of normally differentiated cells of the corresponding lineage, indicating that incomplete differentiation had occurred.
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spelling pubmed-21118562008-05-01 Isoenzymes of lactate dehydrogenase in human leukemic cells in culture treated with inducers of differentiation J Cell Biol Articles The human leukemic cell lines HL60 and K562, were induced to differentiate terminally by chemical agents. The isoenzyme patterns of lactate dehydrogenase (LD) in the cells before and after differentiation were determined electrophoretically on agarose gels. In general, treatment of the leukemic cells with inducers of differentiation resulted in a quantitative shift of the isoenzyme pattern towards anodic or cathodic forms. This was correlated with the conversion of the chemically treated cells to morphologically more normal cells, as verified by light microscopy and/or synthesis of hemoglobin. The LD isoenzyme patterns of the chemically differentiated cells were: (a) characteristic for the particular cell type obtained rather than for the nature of the inducer used; and (b) not similar to those of normally differentiated cells of the corresponding lineage, indicating that incomplete differentiation had occurred. The Rockefeller University Press 1981-08-01 /pmc/articles/PMC2111856/ /pubmed/6945307 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Isoenzymes of lactate dehydrogenase in human leukemic cells in culture treated with inducers of differentiation
title Isoenzymes of lactate dehydrogenase in human leukemic cells in culture treated with inducers of differentiation
title_full Isoenzymes of lactate dehydrogenase in human leukemic cells in culture treated with inducers of differentiation
title_fullStr Isoenzymes of lactate dehydrogenase in human leukemic cells in culture treated with inducers of differentiation
title_full_unstemmed Isoenzymes of lactate dehydrogenase in human leukemic cells in culture treated with inducers of differentiation
title_short Isoenzymes of lactate dehydrogenase in human leukemic cells in culture treated with inducers of differentiation
title_sort isoenzymes of lactate dehydrogenase in human leukemic cells in culture treated with inducers of differentiation
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2111856/
https://www.ncbi.nlm.nih.gov/pubmed/6945307