Scornik F S, Codina J, Birnbaumer L, Toro L
Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, Texas 77030.
Am J Physiol. 1993 Oct;265(4 Pt 2):H1460-5. doi: 10.1152/ajpheart.1993.265.4.H1460.
The occupancy of beta-receptors in the smooth muscle membrane of the coronary arteries produces vasodilation and a concomitant hyperpolarization. Large conductance calcium-activated K (KCa) channels are likely to be involved in such hyperpolarization, since they are densely distributed in coronary myocytes, and they are targets of beta-adrenergic stimulation in other smooth muscles. We sought to explore if coronary smooth muscle KCa channels are modulated by beta-agonists and we studied the mechanisms of their activation. We found that KCa channels reconstituted into lipid bilayers were activated in the presence of GTP by the beta-adrenergic receptor agonist isoproterenol. KCa channels were also stimulated on non-specific activation of an endogenous G protein(s) with guanosine 5'-O-(3-thiotriphosphate) (GTP gamma S), on addition of a purified activated stimulatory G protein (Gs alpha), and when the catalytic subunit of protein kinase A (PKA) was added. Inhibition of PKA activity prevented KCa channel stimulation by PKA, but not by endogenous G protein or by exogenous Gs alpha. These results indicate that beta-adrenoceptor activation of coronary smooth muscle KCa channels results from a dual control: 1) a membrane delimited, possibly direct action of Gs, independent of PKA-mediated phosphorylation; and 2) by PKA-dependent phosphorylation.
冠状动脉平滑肌膜中β受体的占据会导致血管舒张和随之而来的超极化。大电导钙激活钾(KCa)通道可能参与这种超极化,因为它们在冠状动脉心肌细胞中密集分布,并且它们是其他平滑肌中β-肾上腺素能刺激的靶点。我们试图探究冠状动脉平滑肌KCa通道是否受β激动剂调节,并研究其激活机制。我们发现,在脂质双分子层中重组的KCa通道在存在GTP的情况下被β-肾上腺素能受体激动剂异丙肾上腺素激活。用鸟苷5'-O-(3-硫代三磷酸)(GTPγS)非特异性激活内源性G蛋白时,添加纯化的活化刺激性G蛋白(Gsα)以及添加蛋白激酶A(PKA)的催化亚基时,KCa通道也会受到刺激。抑制PKA活性可阻止PKA对KCa通道的刺激,但不能阻止内源性G蛋白或外源性Gsα对其的刺激。这些结果表明,冠状动脉平滑肌KCa通道的β-肾上腺素能受体激活源于双重控制:1)Gs的膜限定性、可能是直接作用,独立于PKA介导的磷酸化;2)通过PKA依赖性磷酸化。