Source:http://linkedlifedata.com/resource/pubmed/id/11732330
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-3
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pubmed:dateCreated |
2001-12-4
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pubmed:abstractText |
Ascorbate has been related to the differentiation of several mesenchymal cells including haematopoietic cells. We have previously demonstrated that ascorbate enhances the activity of 1 alpha,25-dihydroxyvitamin D3 (1 alpha,25(OH)2D3) on monocytic differentiation of HL-60 cells. Here, we show that ascorbate-mediated modification of cellular redox state and AP-1 (activating protein-1) DNA binding during early phases are related to the enhancing effect of ascorbate on differentiation. Ascorbate, but not its fully oxidized form, dehydroascorbate, or an ascorbate analogue with a low rate of oxidation, ascorbate-2-phosphate, enhanced the differentiation induced by 1 alpha,25(OH)2D3, modified cytosolic reactive oxygen species levels and mitochondrial redox potential (delta psi m), and modulated AP-1 DNA binding in HL-60 cells. Ascorbate itself increased AP-1 binding to DNA in noninduced cells, whereas it inhibited AP-1 binding in 1 alpha,25(OH)2D3-induced cells. However, ascorbate increased the mRNA levels of c-jun, junB, and c-fos in 1 alpha,25(OH)2D3-induced cells. Taken together, these results suggest that the enhancing effect of ascorbate on HL-60 differentiation induced by 1 alpha, 25(OH)2D3 is related to its effect on the cellular redox state and the modulation of AP-1 activity.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Ascorbic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Calcitriol,
http://linkedlifedata.com/resource/pubmed/chemical/DNA,
http://linkedlifedata.com/resource/pubmed/chemical/Ethanol,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-fos,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-jun,
http://linkedlifedata.com/resource/pubmed/chemical/Reactive Oxygen Species,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factor AP-1
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pubmed:status |
MEDLINE
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pubmed:issn |
0033-183X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
217
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
129-36
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11732330-Ascorbic Acid,
pubmed-meshheading:11732330-Calcitriol,
pubmed-meshheading:11732330-Cell Differentiation,
pubmed-meshheading:11732330-DNA,
pubmed-meshheading:11732330-Ethanol,
pubmed-meshheading:11732330-HL-60 Cells,
pubmed-meshheading:11732330-Humans,
pubmed-meshheading:11732330-Membrane Potentials,
pubmed-meshheading:11732330-Mitochondria,
pubmed-meshheading:11732330-Monocytes,
pubmed-meshheading:11732330-Oxidation-Reduction,
pubmed-meshheading:11732330-Proto-Oncogene Proteins c-fos,
pubmed-meshheading:11732330-Proto-Oncogene Proteins c-jun,
pubmed-meshheading:11732330-Reactive Oxygen Species,
pubmed-meshheading:11732330-Transcription Factor AP-1
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pubmed:year |
2001
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pubmed:articleTitle |
Cellular redox state and activating protein-1 are involved in ascorbate effect on calcitriol-induced differentiation.
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pubmed:affiliation |
Laboratorio Andaluz de Biología, Universidad Pablo de Olavide, Sevilla, Carretera de Utrera, Km 1.0, 41013 Sevilla, Spain.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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