Source:http://linkedlifedata.com/resource/pubmed/id/12759348
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
31
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pubmed:dateCreated |
2003-7-28
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pubmed:abstractText |
The balance and cross-talk between natruretic and antinatruretic hormone receptors plays a critical role in the regulation of renal Na+ homeostasis, which is a major determinant of blood pressure. Dopamine and angiotensin II have antagonistic effects on renal Na+ and water excretion, which involves regulation of the Na+,K+-ATPase activity. Herein we demonstrate that angiotensin II (Ang II) stimulation of AT1 receptors in proximal tubule cells induces the recruitment of Na+,K+-ATPase molecules to the plasmalemma, in a process mediated by protein kinase Cbeta and interaction of the Na+,K+-ATPase with adaptor protein 1. Ang II stimulation led to phosphorylation of the alpha subunit Ser-11 and Ser-18 residues, and substitution of these amino acids with alanine residues completely abolished the Ang II-induced stimulation of Na+,K+-ATPase-mediated Rb+ transport. Thus, for Ang II-dependent stimulation of Na+,K+-ATPase activity, phosphorylation of these serine residues is essential and may constitute a triggering signal for recruitment of Na+,K+-ATPase molecules to the plasma membrane. When cells were treated simultaneously with saturating concentrations of dopamine and Ang II, either activation or inhibition of the Na+,K+-ATPase activity was produced dependent on the intracellular Na+ concentration, which was varied in a very narrow physiological range (9-19 mm). A small increase in intracellular Na+ concentrations induces the recruitment of D1 receptors to the plasma membrane and a reduction in plasma membrane AT1 receptors. Thus, one or more proteins may act as an intracellular Na+ concentration sensor and play a major regulatory role on the effect of hormones that regulate proximal tubule Na+ reabsorption.
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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/Angiotensin II,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase C,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Angiotensin, Type 1,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Angiotensin,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Dopamine D1,
http://linkedlifedata.com/resource/pubmed/chemical/Rubidium,
http://linkedlifedata.com/resource/pubmed/chemical/Serine,
http://linkedlifedata.com/resource/pubmed/chemical/Sodium,
http://linkedlifedata.com/resource/pubmed/chemical/Sodium-Potassium-Exchanging ATPase,
http://linkedlifedata.com/resource/pubmed/chemical/Tetradecanoylphorbol Acetate,
http://linkedlifedata.com/resource/pubmed/chemical/protein kinase C beta
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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 |
1
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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 |
28719-26
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:12759348-Absorption,
pubmed-meshheading:12759348-Angiotensin II,
pubmed-meshheading:12759348-Animals,
pubmed-meshheading:12759348-Cell Line,
pubmed-meshheading:12759348-Cell Membrane,
pubmed-meshheading:12759348-Dopamine,
pubmed-meshheading:12759348-Epithelial Cells,
pubmed-meshheading:12759348-Homeostasis,
pubmed-meshheading:12759348-Kidney,
pubmed-meshheading:12759348-Kidney Tubules, Proximal,
pubmed-meshheading:12759348-Opossums,
pubmed-meshheading:12759348-Phosphorylation,
pubmed-meshheading:12759348-Protein Kinase C,
pubmed-meshheading:12759348-Receptor, Angiotensin, Type 1,
pubmed-meshheading:12759348-Receptors, Angiotensin,
pubmed-meshheading:12759348-Receptors, Dopamine D1,
pubmed-meshheading:12759348-Rubidium,
pubmed-meshheading:12759348-Serine,
pubmed-meshheading:12759348-Signal Transduction,
pubmed-meshheading:12759348-Sodium,
pubmed-meshheading:12759348-Sodium-Potassium-Exchanging ATPase,
pubmed-meshheading:12759348-Tetradecanoylphorbol Acetate,
pubmed-meshheading:12759348-Transfection
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pubmed:year |
2003
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pubmed:articleTitle |
Intracellular Na+ regulates dopamine and angiotensin II receptors availability at the plasma membrane and their cellular responses in renal epithelia.
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pubmed:affiliation |
College of Pharmacy, University of Houston, Houston, Texas 77204, 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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