Source:http://linkedlifedata.com/resource/pubmed/id/21139376
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2010-12-8
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pubmed:abstractText |
The biologically active form of vitamin D, 1?,25-dihydroxy vitamin D? (VD), regulates the synthesis of the bone Ca-binding proteins osteocalcin and osteopontin. The actions of VD are mediated through the vitamin D receptor (VDR). Liganded VDR heterodimerizes with the retinoid X receptor and interacts with a vitamin D response element (VDRE). Recently, it has been demonstrated that vitamin D responses elicited in osteoblasts can be rapid as well as long-term. The purpose of this study was to elucidate the mechanism of Ca(2+) signaling of VD in osteoblasts using intracellular Ca(2+) ([Ca(2+)]i) measurements. A rapid VD (10 nM)-induced increase in [Ca(2+)]i was observed within 40 sec. This increase, however, was negated with application of Ca(2+)-free Krebs' solution. These results indicate that VD induces an increase in [Ca(2+)]i from extracellular Ca(2+) in osteoblasts.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
D
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0040-8891
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
51
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
221-6
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pubmed:meshHeading |
pubmed-meshheading:21139376-3T3 Cells,
pubmed-meshheading:21139376-Animals,
pubmed-meshheading:21139376-Calcitriol,
pubmed-meshheading:21139376-Calcium,
pubmed-meshheading:21139376-Calcium Channels,
pubmed-meshheading:21139376-Calcium Signaling,
pubmed-meshheading:21139376-Mice,
pubmed-meshheading:21139376-Osteoblasts,
pubmed-meshheading:21139376-Receptors, Calcitriol,
pubmed-meshheading:21139376-Vitamin D Response Element
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pubmed:year |
2010
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pubmed:articleTitle |
1?,25-dihydroxyvitamin D? rapidly modulates Ca(2+) influx in osteoblasts mediated by Ca(2+) channels.
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pubmed:affiliation |
Department of Orthodontics, Tokyo Dental College, Chiba, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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