Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
18
pubmed:dateCreated
2010-4-26
pubmed:abstractText
Dopamine inhibited phosphate transport in isolated renal brush border membrane vesicles and in cultured renal proximal tubule cells from wild-type but not from NHERF-1 null mice. Co-immunoprecipitation experiments established that NHERF-1 associated with D1-like receptors. In wild-type mice, dopamine stimulated cAMP accumulation and protein kinase C (PKC) activity in renal proximal tubule cells, an effect that was abolished by SCH-23390, a D1-like receptor antagonist. In NHERF-1 null kidney tissue; however, dopamine failed to stimulate either cAMP accumulation or PKC activity. Infection of proximal tubule cells from NHERF-1 null mice with adenovirus-green fluorescent protein-NHERF-1 restored the ability of dopamine to stimulate cAMP and PKC. Finally, in (32)P-labeled wild-type proximal tubule cells and in opossum kidney cells, dopamine increased NHERF-1 phosphorylation at serine 77 of the PDZ I domain of NHERF-1, a site previously shown to attenuate binding of cellular targets including the Npt2a (sodium-dependent phosphate transporter 2a). Together, these studies establish that NHERF-1 plays a key role in dopamine signaling and is also a downstream target of D1-like receptors in the mouse kidney. These studies suggest a novel role for the PDZ adapter protein NHERF-1 in coordinating dopamine signals that inhibit renal phosphate transport.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-11997325, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-12075354, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-12169661, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-12192091, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-12193606, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-12386143, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-12586353, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-12917102, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-14706863, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-14907713, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-14976410, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-15037630, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-15070904, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-15547113, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-15890704, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-16460281, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-16705152, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-17369255, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-17580307, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-17895247, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-17975671, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-18202147, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-18615257, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-18987113, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-9560162, http://linkedlifedata.com/resource/pubmed/commentcorrection/20200151-9621280
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1083-351X
pubmed:author
pubmed:issnType
Electronic
pubmed:day
30
pubmed:volume
285
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
13454-60
pubmed:dateRevised
2011-7-28
pubmed:meshHeading
pubmed-meshheading:20200151-Adenoviridae, pubmed-meshheading:20200151-Animals, pubmed-meshheading:20200151-Dopamine, pubmed-meshheading:20200151-Dopamine Agents, pubmed-meshheading:20200151-Ion Transport, pubmed-meshheading:20200151-Kidney Tubules, Proximal, pubmed-meshheading:20200151-Mice, pubmed-meshheading:20200151-Mice, Knockout, pubmed-meshheading:20200151-Opossums, pubmed-meshheading:20200151-Phosphates, pubmed-meshheading:20200151-Phosphoproteins, pubmed-meshheading:20200151-Phosphorylation, pubmed-meshheading:20200151-Protein Kinase C, pubmed-meshheading:20200151-Receptors, Dopamine D1, pubmed-meshheading:20200151-Signal Transduction, pubmed-meshheading:20200151-Sodium, pubmed-meshheading:20200151-Sodium-Hydrogen Antiporter, pubmed-meshheading:20200151-Sodium-Phosphate Cotransporter Proteins, Type IIa
pubmed:year
2010
pubmed:articleTitle
Sodium-hydrogen exchanger regulatory factor 1 (NHERF-1) transduces signals that mediate dopamine inhibition of sodium-phosphate co-transport in mouse kidney.
pubmed:affiliation
Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA. eweinman1440@yahoo.com
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural