Department of Pharmacology, Graduate School of Medicine and The Center for Advanced Medical Engineering and Informatics, Osaka University, Osaka 565-0871, Japan.
Physiol Rev. 2010 Jan;90(1):291-366. doi: 10.1152/physrev.00021.2009.
Inwardly rectifying K(+) (Kir) channels allow K(+) to move more easily into rather than out of the cell. They have diverse physiological functions depending on their type and their location. There are seven Kir channel subfamilies that can be classified into four functional groups: classical Kir channels (Kir2.x) are constitutively active, G protein-gated Kir channels (Kir3.x) are regulated by G protein-coupled receptors, ATP-sensitive K(+) channels (Kir6.x) are tightly linked to cellular metabolism, and K(+) transport channels (Kir1.x, Kir4.x, Kir5.x, and Kir7.x). Inward rectification results from pore block by intracellular substances such as Mg(2+) and polyamines. Kir channel activity can be modulated by ions, phospholipids, and binding proteins. The basic building block of a Kir channel is made up of two transmembrane helices with cytoplasmic NH(2) and COOH termini and an extracellular loop which folds back to form the pore-lining ion selectivity filter. In vivo, functional Kir channels are composed of four such subunits which are either homo- or heterotetramers. Gene targeting and genetic analysis have linked Kir channel dysfunction to diverse pathologies. The crystal structure of different Kir channels is opening the way to understanding the structure-function relationships of this simple but diverse ion channel family.
内向整流钾 (Kir) 通道允许钾更容易进入而不是流出细胞。它们具有多种生理功能,具体取决于其类型和位置。有七种 Kir 通道亚家族,可分为四个功能组:经典 Kir 通道 (Kir2.x) 是组成型激活的,G 蛋白门控 Kir 通道 (Kir3.x) 受 G 蛋白偶联受体调节,ATP 敏感性钾 (Kir6.x) 与细胞代谢紧密相关,以及钾转运通道 (Kir1.x、Kir4.x、Kir5.x 和 Kir7.x)。内向整流是由于细胞内物质(如 Mg2+和多胺)阻塞孔道而产生的。Kir 通道的活性可以通过离子、磷脂和结合蛋白来调节。Kir 通道的基本组成部分是由两个跨膜螺旋组成,带有细胞质 NH2 和 COOH 末端和一个细胞外环,该环折叠回形成孔道衬里的离子选择性过滤器。在体内,功能性 Kir 通道由四个这样的亚基组成,这些亚基可以是同源或异源四聚体。基因靶向和遗传分析已经将 Kir 通道功能障碍与多种病理学联系起来。不同 Kir 通道的晶体结构为理解这个简单但多样化的离子通道家族的结构-功能关系开辟了道路。