Division of Cardiovascular Medicine, Department of Internal Medicine, University of Iowa Carver College of Medicine, Iowa City, Iowa 52242, USA.
J Biol Chem. 2010 Sep 10;285(37):28723-30. doi: 10.1074/jbc.M110.147868. Epub 2010 Jul 7.
Ankyrin polypeptides are critical for normal membrane protein expression in diverse cell types, including neurons, myocytes, epithelia, and erythrocytes. Ankyrin dysfunction results in defects in membrane expression of ankyrin-binding partners (including ion channels, transporters, and cell adhesion molecules), resulting in aberrant cellular function and disease. Here, we identify a new role for ankyrin-B in cardiac cell biology. We demonstrate that cardiac sarcolemmal K(ATP) channels directly associate with ankyrin-B in heart via the K(ATP) channel alpha-subunit Kir6.2. We demonstrate that primary myocytes lacking ankyrin-B display defects in Kir6.2 protein expression, membrane expression, and function. Moreover, we demonstrate a secondary role for ankyrin-B in regulating K(ATP) channel gating. Finally, we demonstrate that ankyrin-B forms a membrane complex with K(ATP) channels and the cardiac Na/K-ATPase, a second key membrane transporter involved in the cardiac ischemia response. Collectively, our new findings define a new role for cardiac ankyrin polypeptides in regulation of ion channel membrane expression in heart.
锚蛋白多肽对于多种细胞类型(包括神经元、心肌细胞、上皮细胞和红细胞)中正常的膜蛋白表达至关重要。锚蛋白功能障碍导致锚蛋白结合伴侣(包括离子通道、转运体和细胞黏附分子)的膜表达缺陷,导致细胞功能异常和疾病。在这里,我们确定了锚蛋白-B 在心脏细胞生物学中的一个新作用。我们证明了心脏肌质网 K(ATP) 通道通过 K(ATP) 通道的α亚基 Kir6.2 直接与心脏中的锚蛋白-B 结合。我们证明缺乏锚蛋白-B 的原代心肌细胞显示 Kir6.2 蛋白表达、膜表达和功能缺陷。此外,我们证明了锚蛋白-B 在调节 K(ATP) 通道门控方面的次要作用。最后,我们证明了锚蛋白-B 与 K(ATP) 通道和心脏 Na/K-ATP 酶形成膜复合物,后者是参与心脏缺血反应的第二个关键膜转运体。总之,我们的新发现定义了心脏锚蛋白多聚体在调节心脏离子通道膜表达中的新作用。