RGD Reference Report - Heteromultimeric Kv1 channels contribute to myogenic control of arterial diameter. - Rat Genome Database

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Heteromultimeric Kv1 channels contribute to myogenic control of arterial diameter.

Authors: Plane, F  Johnson, R  Kerr, P  Wiehler, W  Thorneloe, K  Ishii, K  Chen, T  Cole, W 
Citation: Plane F, etal., Circ Res. 2005 Feb 4;96(2):216-24. Epub 2004 Dec 23.
RGD ID: 10047274
Pubmed: PMID:15618540   (View Abstract at PubMed)
DOI: DOI:10.1161/01.RES.0000154070.06421.25   (Journal Full-text)

Inhibition of vascular smooth muscle (VSM) delayed rectifier K+ channels (K(DR)) by 4-aminopyridine (4-AP; 200 micromol/L) or correolide (1 micromol/L), a selective inhibitor of Kv1 channels, enhanced myogenic contraction of rat mesenteric arteries (RMAs) in response to increases in intraluminal pressure. The molecular identity of K(DR) of RMA myocytes was characterized using RT-PCR, real-time PCR, and immunocytochemistry. Transcripts encoding the pore-forming Kvalpha subunits, Kv1.2, Kv1.4, Kv1.5, and Kv1.6, were identified and confirmed at the protein level with subunit-specific antibodies. Kvbeta transcript (beta1.1, beta1.2, beta1.3, and beta2.1) expression was also identified. Kv1.5 message was approximately 2-fold more abundant than that for Kv1.2 and Kv1.6. Transcripts encoding these three Kv1alpha subunits were approximately 2-fold more abundant in 1st/2nd order conduit compared with 4th order resistance RMAs, and Kvbeta1 was 8-fold higher than Kvbeta2 message. RMA K(DR) activated positive to -50 mV, exhibited incomplete inactivation, and were inhibited by 4-AP and correolide. However, neither alpha-dendrotoxin or kappa-dendrotoxin affected RMA K(DR), implicating the presence of Kv1.5 in all channels and the absence of Kv1.1, respectively. Currents mediated by channels because of coexpression of Kv1.2, Kv1.5, Kv1.6, and Kvbeta1.2 in human embryonic kidney 293 cells had biophysical and pharmacological properties similar to those of RMA K(DR). It is concluded that K(DR) channels composed of heteromultimers of Kv1 subunits play a critical role in myogenic control of arterial diameter.

Gene Ontology Annotations    Click to see Annotation Detail View

Biological Process
TermQualifierEvidenceWithReferenceNotesSourceOriginal Reference(s)
potassium ion transmembrane transport involved_inIDA 10047274; 10047274PMID:15618540UniProt 

Cellular Component
TermQualifierEvidenceWithReferenceNotesSourceOriginal Reference(s)
plasma membrane located_inIMP 10047274; 10047274PMID:15618540UniProt 
voltage-gated potassium channel complex part_ofIDA 10047274; 10047274PMID:15618540UniProt 

Molecular Function
TermQualifierEvidenceWithReferenceNotesSourceOriginal Reference(s)
delayed rectifier potassium channel activity enablesIDA 10047274; 10047274PMID:15618540UniProt 

Objects Annotated

Genes (Rattus norvegicus)
Kcna5  (potassium voltage-gated channel subfamily A member 5)
Kcna6  (potassium voltage-gated channel subfamily A member 6)


Additional Information