Source:http://linkedlifedata.com/resource/pubmed/id/19748978
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2009-9-21
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pubmed:abstractText |
The PI3K pathway plays a pivotal role in the stimulation of mast cells. PI3K-dependent kinases include the serum- and glucocorticoid-inducible kinase 1 (SGK1). The present study explored the role of SGK1 in mast cell function. Mast cells were isolated from bone marrow (BMMC) of SGK1 knockout mice (sgk1(-/-)) and their wild-type littermates (sgk1(+/+)). The BMMC number as well as CD117, CD34, and FcepsilonRI expression in BMCCs were similar in both genotypes. Upon Ag stimulation of the FcepsilonRI receptor, Ca(2+) entry but not Ca(2+) release from intracellular stores was markedly impaired in sgk1(-/-) BMMCs. The currents through Ca(2+)-activated K+ channels induced by Ag were significantly higher in sgk1(+/+) BMMCs than in sgk1(-/-) BMMCs. Treatment with the Ca(2+) ionophore ionomycin (1 microM) led to activation of the K+ channels in both genotypes, indicating that the Ca(2+)-activated K+ channels are similarly expressed and sensitive to activation by Ca(2+) in sgk1(+/+) and sgk1(-/-) BMMCs, and that blunted stimulation of Ca(2+)-activated K+ channels was secondary to decreased Ca(2+) entry. Ag-IgE-induced degranulation and early IL-6 secretion were also significantly blunted in sgk1(-/-) BMMCs. The decrease in body temperature following Ag treatment, which reflects an anaphylactic reaction, was substantially reduced in sgk1(-/-) mice, pointing to impaired mast cell function in vivo. Serum histamine levels measured 30 min after induction of an anaphylactic reaction were significantly lower in sgk1(-/-) than in sgk1(+/+)mice. The observations reveal a critical role for SGK1 in ion channel regulation and the function of mast cells, and thus disclose a completely novel player in the regulation of allergic reaction.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Immediate-Early Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphatidylinositol 3-Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Potassium Channels...,
http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/serum-glucocorticoid regulated...
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1550-6606
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pubmed:author |
pubmed-author:BiedermannTiloT,
pubmed-author:KaeslerSusanneS,
pubmed-author:KuhlDietmarD,
pubmed-author:LamRebecca SRS,
pubmed-author:LangFlorianF,
pubmed-author:LupescuAdrianA,
pubmed-author:MatznerNicoleN,
pubmed-author:SchallerMartinM,
pubmed-author:ShumilinaEkaterinaE,
pubmed-author:SobiesiakMalgorzataM,
pubmed-author:WölbingFlorianF,
pubmed-author:ZahirNaimaN,
pubmed-author:ZemtsovaIrina MIM
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pubmed:issnType |
Electronic
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pubmed:day |
1
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pubmed:volume |
183
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4395-402
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pubmed:dateRevised |
2011-11-2
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pubmed:meshHeading |
pubmed-meshheading:19748978-Anaphylaxis,
pubmed-meshheading:19748978-Animals,
pubmed-meshheading:19748978-Bone Marrow Cells,
pubmed-meshheading:19748978-Cells, Cultured,
pubmed-meshheading:19748978-Female,
pubmed-meshheading:19748978-Gene Targeting,
pubmed-meshheading:19748978-Immediate-Early Proteins,
pubmed-meshheading:19748978-Male,
pubmed-meshheading:19748978-Mast Cells,
pubmed-meshheading:19748978-Mice,
pubmed-meshheading:19748978-Mice, Inbred C57BL,
pubmed-meshheading:19748978-Mice, Knockout,
pubmed-meshheading:19748978-Phosphatidylinositol 3-Kinases,
pubmed-meshheading:19748978-Potassium Channels, Calcium-Activated,
pubmed-meshheading:19748978-Protein-Serine-Threonine Kinases
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pubmed:year |
2009
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pubmed:articleTitle |
Impaired mast cell activation in gene-targeted mice lacking the serum- and glucocorticoid-inducible kinase SGK1.
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pubmed:affiliation |
Department of Physiology, University of Tübingen, Tübingen D-72076, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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