Molecular basis of native voltage-dependent K+ (Kv) channels in smooth musc
le cells (SMCs) from rat mesenteric arteries was investigated. The whole ce
ll patch-clamp study revealed that a 4-aminopyridine-sensitive delayed rect
ifier K+ current (I-K) was the predominant K+ conductance in these cells. A
systematic screening of the expression of 18 Kv channel genes using RT-PCR
technique showed that six I-K-encoding genes (Kv1.2, Kv1.3, Kv1.5, Kv2.1,
Kv2.2, and Kv3.2) were expressed in mesenteric artery. Although no transien
t outward Kv currents (I-A) were recorded in the studied SMCs, transcripts
of multiple I-A-encoding genes, including Kv1.4, Kv3.3, Kv3.4, Kv4.1, Kv4.2
, and Kv4.3 as well as I-A-facilitating Kv beta-subunits (Kv beta 1, Kv bet
a 2, and Kv beta 3), were detected in mesenteric arteries. Western blot ana
lysis demonstrated that four I-K-related Kv channel proteins (Kv1.2, Kv1.3,
Kv1.5, and Kv2.1) were detected in mesenteric artery tissues. The presence
of Kv1.2, Kv1.3, Kv1.5, and Kv2.1 channel proteins in isolated SMCs was fu
rther confirmed by immunocytochemistry study. Our results suggest that the
native I-K in rat mesenteric artery SMCs might be generated by heteromultim
erization of Kv genes.