An Apamin- and Scyllatoxin-Insensitive Isoform of the Human SK3 Channel

• Published in: Molecular pharmacology 2004-03, Vol.65 (3), p.788-801
• Main Authors: Wittekindt, Oliver H., Visan, Violeta, Tomita, Hiroaki, Imtiaz, Faiqa, Gargus, Jay J., Lehmann-Horn, Frank, Grissmer, Stephan, Morris-Rosendahl, Deborah J.
• Format: Article
• Language: English
• Subjects: Alternative Splicing; Apamin - pharmacology; Barium - pharmacology; Benzimidazoles - pharmacology; Calcium - metabolism; Humans; Potassium Channels - drug effects; Potassium Channels - metabolism; Potassium Channels, Calcium-Activated; Protein Isoforms - drug effects; Protein Isoforms - metabolism; Reverse Transcriptase Polymerase Chain Reaction; Scorpion Venoms - pharmacology; Small-Conductance Calcium-Activated Potassium Channels; Tetraethylammonium - pharmacology; Tubocurarine - pharmacology
• ISSN: 0026-895X; 1521-0111
• DOI: 10.1124/mol.65.3.788

We have isolated an hSK3 isoform from a human embryonic cDNA library that we have named hSK3_ex4. This isoform contains a 15 amino acid insertion within the S5 to P-loop segment. Transcripts encoding hSK3_ex4 are coexpressed at lower levels with hSK3 in neuronal as well as in non-neuronal tissues. To investigate the pharmacokinetic properties of hSK3_ex4, we expressed the isoforms hSK3 and hSK3_ex4 in tsA cells. Both isoforms were similarly activated by cytosolic Ca2+ (hSK3, EC50 = 0.91 ± 0.4 μM; hSK3_ex4, EC50 = 0.78 ± 0.2 μM) and by 1-ethyl-2-benzimidazolinone (hSK3, EC50 = 0.17 mM; hSK3_ex4, 0.19 mM). They were both blocked by tetraethylammonium (hSK3, Kd = 2.2 mM; hSK3_ex4, 2.6 mM) and showed similar permeabilities relative to K+ for Cs+ (hSK3, 0.17 ± 0.04, n = 3; hSK3_ex4, 0.17 ± 0.05, n = 3) and Rb+ (hSK3, 0.79 ± 0.04, n = 3; hSK3_ex4, 0.8 ± 0.07, n = 3). Ba2+ blocked both isoforms, and in both cases, the block was strongest at hyperpolarizing membrane potentials. However, the voltage-dependence of hSK3 was stronger than that of hSK3_ex4. The most obvious distinguishing feature of this new isoform was that whereas hSK3 was blocked by apamin (Kd = 0.8 nM), scyllatoxin (Kd = 2.1 nM), and d-tubocurarine (Kd = 33.4 μM), hSK3_ex4 was not affected by apamin up to 100 nM, scyllatoxin up to 500 nM, and d-tubocurarine up to 500 μM. So far, isoform hSK3_ex4 forms the only small-conductance calcium-activated potassium (SK) channels, which are insensitive to the classic SK blockers.