Ehrlich B E, Watras J
Department of Medicine, University of Connecticut, Farmington 06032.
Nature. 1988 Dec 8;336(6199):583-6. doi: 10.1038/336583a0.
Inositol 1,4,5-trisphosphate (InsP3) can initiate calcium release into the cytoplasm in a variety of cells. From experiments using permeabilized cells, membrane vesicles, and patch-clamp techniques, it has been suggested that InsP3 acts by directly opening calcium channels. Here, we show that InsP3 induced openings of channels in planar lipid bilayers into which vesicles made from aortic muscle sarcoplasmic reticulum (SR) were incorporated. Activation of channels by InsP3 was not observed when vesicles made from SR of cardiac or skeletal muscle were incorporated into planar lipid bilayers. The present study demonstrates for the first time unique properties of an InsP3-gated calcium channel in sarcoplasmic reticulum vesicles from vascular smooth muscle. This InsP3-activated channel from aortic SR differs strikingly from the calcium-gated calcium channel of striated muscle SR in single-channel conductance and pharmacology.
肌醇1,4,5 -三磷酸(InsP3)可引发多种细胞的细胞质中钙离子的释放。通过使用通透细胞、膜囊泡和膜片钳技术的实验表明,InsP3通过直接打开钙通道发挥作用。在此,我们展示了InsP3可诱导由主动脉肌浆网(SR)制成的囊泡整合其中的平面脂质双分子层中的通道开放。当将心肌或骨骼肌的SR制成的囊泡整合到平面脂质双分子层中时,未观察到InsP3对通道的激活作用。本研究首次证明了血管平滑肌肌浆网囊泡中InsP3门控钙通道的独特性质。来自主动脉SR的这种InsP3激活通道在单通道电导和药理学方面与横纹肌SR的钙门控钙通道显著不同。