Source:http://linkedlifedata.com/resource/pubmed/id/10681540
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
8
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| pubmed:dateCreated |
2000-3-30
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| pubmed:abstractText |
The sst2A receptor is expressed in the endocrine, gastrointestinal, and neuronal systems as well as in many hormone-sensitive tumors. This receptor is rapidly internalized and phosphorylated in growth hormone-R2 pituitary cells following somatostatin binding (Hipkin, R. W., Friedman, J., Clark, R. B., Eppler, C. M., and Schonbrunn, A. (1997) J. Biol. Chem. 272, 13869-13876). The protein kinase C (PKC) activator, phorbol 12-myristate 13-acetate (PMA), also stimulates sst2A phosphorylation. Here we examine the mechanisms and consequences of PMA and agonist-induced sst2A phosphorylation. Like somatostatin, both PMA and bombesin increased sst2A receptor phosphorylation within 2 min. The PKC inhibitor GF109203X blocked PMA- and bombesin- stimulated sst2A phosphorylation, whereas stimulation by the somatostatin analog SMS 201-995 was unaffected. Agonist and PMA each stimulated phosphorylation in two receptor domains, the third intracellular loop and the C-terminal tail. Functionally, PMA dramatically increased the internalization of the sst2A receptor-ligand complex. This PMA stimulation was blocked by GF109203X, whereas basal internalization was unaffected. However, neither basal nor PMA-stimulated internalization was altered by pertussis toxin, whereas both were blocked by hypertonic sucrose. Therefore PKC activation and agonist binding stimulate sst2A phosphorylation by distinct mechanisms, and PKC potentiates internalization of the sst2A receptor via clathrin-coated pits. Thus, hormonal stimulation of PKC-coupled receptors may provide a mechanism for regulating the inhibitory actions of somatostatin in target tissue.
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| pubmed:grant | |
| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:citationSubset |
IM
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| pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Bombesin,
http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase C,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Somatostatin,
http://linkedlifedata.com/resource/pubmed/chemical/Tetradecanoylphorbol Acetate,
http://linkedlifedata.com/resource/pubmed/chemical/somatostatin receptor sst2A
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| pubmed:status |
MEDLINE
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| pubmed:month |
Feb
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| pubmed:issn |
0021-9258
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| pubmed:author | |
| pubmed:issnType |
Print
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| pubmed:day |
25
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| pubmed:volume |
275
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
5591-9
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| pubmed:dateRevised |
2007-11-15
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| pubmed:meshHeading |
pubmed-meshheading:10681540-Animals,
pubmed-meshheading:10681540-Bombesin,
pubmed-meshheading:10681540-Cell Membrane,
pubmed-meshheading:10681540-Dose-Response Relationship, Drug,
pubmed-meshheading:10681540-Enzyme Activation,
pubmed-meshheading:10681540-Enzyme Inhibitors,
pubmed-meshheading:10681540-Humans,
pubmed-meshheading:10681540-Peptide Mapping,
pubmed-meshheading:10681540-Phosphorylation,
pubmed-meshheading:10681540-Pituitary Gland,
pubmed-meshheading:10681540-Protein Kinase C,
pubmed-meshheading:10681540-Protein Structure, Secondary,
pubmed-meshheading:10681540-Rats,
pubmed-meshheading:10681540-Receptors, Somatostatin,
pubmed-meshheading:10681540-Temperature,
pubmed-meshheading:10681540-Tetradecanoylphorbol Acetate,
pubmed-meshheading:10681540-Time Factors,
pubmed-meshheading:10681540-Tumor Cells, Cultured
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| pubmed:year |
2000
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| pubmed:articleTitle |
Protein kinase C activation stimulates the phosphorylation and internalization of the sst2A somatostatin receptor.
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| pubmed:affiliation |
Department of Integrative Biology, University of Texas Health Sciences Center Houston, Houston, Texas 77225, USA.
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| pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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