Characterization of an apamin‐sensitive small‐conductance Ca2+‐activated K+ channel in porcine coronary artery endothelium: relevance to EDHF
MP Burnham, R Bychkov, M Feletou… - British journal of …, 2002 - Wiley Online Library
MP Burnham, R Bychkov, M Feletou, GR Richards, PM Vanhoutte, AH Weston, G Edwards
British journal of pharmacology, 2002•Wiley Online LibraryThe apamin‐sensitive small‐conductance Ca2+‐activated K+ channel (SKCa) was
characterized in porcine coronary arteries. In intact arteries, 100 nm substance P and 600
μm 1‐ethyl‐2‐benzimidazolinone (1‐EBIO) produced endothelial cell hyperpolarizations
(27.8±0.8 mV and 24.1±1.0 mV, respectively). Charybdotoxin (100 nm) abolished the 1‐
EBIO response but substance P continued to induce a hyperpolarization (25.8±0.3 mV). In
freshly‐isolated endothelial cells, outside‐out patch recordings revealed a unitary K+ …
characterized in porcine coronary arteries. In intact arteries, 100 nm substance P and 600
μm 1‐ethyl‐2‐benzimidazolinone (1‐EBIO) produced endothelial cell hyperpolarizations
(27.8±0.8 mV and 24.1±1.0 mV, respectively). Charybdotoxin (100 nm) abolished the 1‐
EBIO response but substance P continued to induce a hyperpolarization (25.8±0.3 mV). In
freshly‐isolated endothelial cells, outside‐out patch recordings revealed a unitary K+ …
- The apamin‐sensitive small‐conductance Ca2+‐activated K+ channel (SKCa) was characterized in porcine coronary arteries.
- In intact arteries, 100 nM substance P and 600 μM 1‐ethyl‐2‐benzimidazolinone (1‐EBIO) produced endothelial cell hyperpolarizations (27.8±0.8 mV and 24.1±1.0 mV, respectively). Charybdotoxin (100 nM) abolished the 1‐EBIO response but substance P continued to induce a hyperpolarization (25.8±0.3 mV).
- In freshly‐isolated endothelial cells, outside‐out patch recordings revealed a unitary K+ conductance of 6.8±0.04 pS. The open‐probability was increased by Ca2+ and reduced by apamin (100 nM). Substance P activated an outward current under whole‐cell perforated‐patch conditions and a component of this current (38%) was inhibited by apamin. A second conductance of 2.7±0.03 pS inhibited by d‐tubocurarine was observed infrequently.
- Messenger RNA encoding the SK2 and SK3, but not the SK1, subunits of SKCa was detected by RT – PCR in samples of endothelium. Western blotting indicated that SK3 protein was abundant in samples of endothelium compared to whole arteries. SK2 protein was present in whole artery nuclear fractions.
- Immunofluorescent labelling confirmed that SK3 was highly expressed at the plasmalemma of endothelial cells and was not expressed in smooth muscle. SK2 was restricted to the peri‐nuclear regions of both endothelial and smooth muscle cells.
- In conclusion, the porcine coronary artery endothelium expresses an apamin‐sensitive SKCa containing the SK3 subunit. These channels are likely to confer all or part of the apamin‐sensitive component of the endothelium‐derived hyperpolarizing factor (EDHF) response.
British Journal of Pharmacology (2002) 135, 1133–1143; doi:10.1038/sj.bjp.0704551
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