Functional Expression Profile of Voltage-Gated K+ Channel Subunits in Rat Small Mesenteric Arteries
Autor: | Robert H. Cox, Samantha J. Fromme |
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Rok vydání: | 2015 |
Předmět: |
Male
0301 basic medicine Contraction (grammar) Protein subunit Biophysics Biochemistry Article Linopirdine 03 medical and health sciences medicine Animals Humans Myocyte Rats Wistar Mesenteric arteries Voltage-gated ion channel Chemistry Organ Size Cell Biology General Medicine Anatomy SMA Mesenteric Arteries Rats Protein Subunits Stromatoxin HEK293 Cells 030104 developmental biology medicine.anatomical_structure Gene Expression Regulation Organ Specificity Potassium Channels Voltage-Gated medicine.drug |
Zdroj: | Cell Biochemistry and Biophysics. 74:263-276 |
ISSN: | 1559-0283 1085-9195 |
DOI: | 10.1007/s12013-015-0715-4 |
Popis: | Multiple K v channel complexes contribute to total K v current in numerous cell types and usually subserve different physiological functions. Identifying the complete compliment of functional K v channel subunits in cells is a prerequisite to understanding regulatory function. It was the goal of this work to determine the complete K v subunit compliment that contribute to functional K v currents in rat small mesenteric artery (SMA) myocytes as a prelude to studying channel regulation. Using RNA prepared from freshly dispersed myocytes, high levels of K v 1.2, 1.5, and 2.1 and lower levels of K v 7.4 α-subunit expressions were demonstrated by quantitative PCR and confirmed by Western blotting. Selective inhibitors correolide (K v 1; COR), stromatoxin (K v 2.1; ScTx), and linopirdine (K v 7.4; LINO) decreased K v current at +40 mV in SMA by 46 ± 4, 48 ± 4, and 6.5 ± 2 %, respectively, and K v current in SMA was insensitive to α-dendrotoxin. Contractions of SMA segments pretreated with 100 nmol/L phenylephrine were enhanced by 27 ± 3, 30 ± 8, and 7 ± 3 % of the response to 120 mmol/L KCl by COR, ScTX, and LINO, respectively. The presence of K v 6.1, 9.3, β1.1, and β1.2 was demonstrated by RT-PCR using myocyte RNA with expressions of K vβ1.2 and K v 9.3 about tenfold higher than K vβ1.1 and K v 6.1, respectively. Selective inhibitors of K v 1.3, 3.4, 4.1, and 4.3 channels also found at the RNA and/or protein level had no significant effect on K v current or contraction. These results suggest that K v current in rat SMA myocytes are dominated equally by two major components consisting of K v 1.2–1.5–β1.2 and K v 2.1–9.3 channels along with a smaller contribution from K v 7.4 channels but differences in voltage dependence of activation allows all three to provide significant contributions to SMA function at physiological voltages. |
Databáze: | OpenAIRE |
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