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Retinoic acid enhances differentiation of v-myb-transformed monoblasts induced by okadaic acid
P. Benes, V. Maceckova, J. Zatloukalova, L. Kovarova, J. Smardova, J. Smarda
Jazyk angličtina Země Velká Británie
NLK
ScienceDirect (archiv)
od 1993-01-01 do 2009-12-31
- MeSH
- aktivace transkripce účinky léků MeSH
- buněčná diferenciace účinky léků MeSH
- financování organizované MeSH
- geny myb MeSH
- imunoblotting MeSH
- kur domácí MeSH
- kyselina okadaová farmakologie MeSH
- leukemie metabolismus MeSH
- makrofágy cytologie účinky léků MeSH
- monocyty cytologie účinky léků MeSH
- nádorové buněčné linie MeSH
- protinádorové látky farmakologie MeSH
- transfekce MeSH
- transformované buněčné linie MeSH
- tretinoin farmakologie MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
Differentiation of various leukemic cells can be induced by liganded retinoic acid receptors and protein phosphatase inhibitors. In this study, we explored the effects of okadaic acid (OA), the phosphatase inhibitor, and retinoic acid (RA) in v-myb-transformed monoblasts BM2. OA induced differentiation of BM2 monoblasts into macrophage-like cells, as documented by analyses of cell morphology, cell cycle, phagocytic activity, non-specific esterase activity, production of reactive oxygen species and expression of vimentin and Mo-1. In contrast to many other leukemic cell lines, BM2 cells do not respond to retinoic acid. However, once exposed to OA and RA simultaneously, BM2 cells differentiate along monocyte/macrophage pathway more efficiently. We conclude that RA enhances differentiation of v-myb-transformed monoblasts induced by protein phosphorylation.
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- $a Differentiation of various leukemic cells can be induced by liganded retinoic acid receptors and protein phosphatase inhibitors. In this study, we explored the effects of okadaic acid (OA), the phosphatase inhibitor, and retinoic acid (RA) in v-myb-transformed monoblasts BM2. OA induced differentiation of BM2 monoblasts into macrophage-like cells, as documented by analyses of cell morphology, cell cycle, phagocytic activity, non-specific esterase activity, production of reactive oxygen species and expression of vimentin and Mo-1. In contrast to many other leukemic cell lines, BM2 cells do not respond to retinoic acid. However, once exposed to OA and RA simultaneously, BM2 cells differentiate along monocyte/macrophage pathway more efficiently. We conclude that RA enhances differentiation of v-myb-transformed monoblasts induced by protein phosphorylation.
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