Source:http://linkedlifedata.com/resource/pubmed/id/12738775
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
34
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pubmed:dateCreated |
2003-8-18
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pubmed:abstractText |
The third intracellular (3i) loops of the alpha 2A- and alpha 2B-adrenergic receptor (AR) subtypes are critical for retention of these receptors at the basolateral surface of polarized Madin-Darby canine kidney (MDCKII) cells at steady state. The third intracellular loops of the alpha 2A, alpha 2B, and alpha 2C-AR subtypes interact with spinophilin, a multidomain protein that, like the three alpha 2-AR subtypes, is enriched at the basolateral surface of MDCKII cells. The present studies provide evidence that alpha 2-AR interaction with spinophilin contributes to cell surface stabilization of the receptor. We exploited the unique targeting profile of the alpha 2B-AR subtype in MDCKII cells: random delivery to apical and basolateral surfaces with rapid (t(1/2) < or = 60 min) apical versus slower (t(1/2) = 10-12 h) basolateral turnover. Apical delivery of a spinophilin subdomain containing the alpha 2-AR-interacting region (Sp151-483) by fusion with apically targeted p75NTR extended the half-life of alpha 2B-AR at the apical surface to approximately 3.6 h and eliminated the rapid phase (0-60 min) of alpha 2B-AR turnover on that surface. Furthermore, we examined alpha 2B-AR turnover at the surface of mouse embryo fibroblasts derived from wild type (Sp+/+) or spinophilin knock-out (Sp-/-) mice. Two independent experimental approaches demonstrated that agonist-evoked internalization of HA-alpha 2B-AR was accelerated in mouse embryo fibroblasts derived from Sp-/- mice. These findings are consistent with the interpretation that endogenous spinophilin contributes to the stabilization of alpha 2B-AR and presumably all three alpha2-AR subtypes at the surface of target cells and may act as a scaffold that could link alpha 2-ARs to proteins interacting with spinophilin via other domains.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/1S10RR15682-1,
http://linkedlifedata.com/resource/pubmed/grant/CA68485,
http://linkedlifedata.com/resource/pubmed/grant/DA10044,
http://linkedlifedata.com/resource/pubmed/grant/DK20593,
http://linkedlifedata.com/resource/pubmed/grant/DK43879,
http://linkedlifedata.com/resource/pubmed/grant/DK58404,
http://linkedlifedata.com/resource/pubmed/grant/GM07628-19,
http://linkedlifedata.com/resource/pubmed/grant/GM07628-20,
http://linkedlifedata.com/resource/pubmed/grant/GM07628-21,
http://linkedlifedata.com/resource/pubmed/grant/MH40899,
http://linkedlifedata.com/resource/pubmed/grant/NS37508
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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/Adrenergic alpha-Agonists,
http://linkedlifedata.com/resource/pubmed/chemical/Microfilament Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Adrenergic, alpha-2,
http://linkedlifedata.com/resource/pubmed/chemical/neurabin
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0021-9258
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
22
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pubmed:volume |
278
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
32405-12
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:12738775-Adrenergic alpha-Agonists,
pubmed-meshheading:12738775-Animals,
pubmed-meshheading:12738775-Cell Line,
pubmed-meshheading:12738775-Cell Membrane,
pubmed-meshheading:12738775-Dogs,
pubmed-meshheading:12738775-Female,
pubmed-meshheading:12738775-Fluorescent Antibody Technique,
pubmed-meshheading:12738775-Mice,
pubmed-meshheading:12738775-Mice, Knockout,
pubmed-meshheading:12738775-Microfilament Proteins,
pubmed-meshheading:12738775-Nerve Tissue Proteins,
pubmed-meshheading:12738775-Pregnancy,
pubmed-meshheading:12738775-Receptors, Adrenergic, alpha-2
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pubmed:year |
2003
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pubmed:articleTitle |
Spinophilin stabilizes cell surface expression of alpha 2B-adrenergic receptors.
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pubmed:affiliation |
Department of Pharmacology, Center for Molecular Neuroscience, Vanderbilt University Medical Center, Nashville, Tennessee 37232-6600, 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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