Department of Physiology and Biophysics, Virginia Commonwealth University, School of Medicine, Richmond, VA 23298, USA.
Pflugers Arch. 2010 Jul;460(2):321-41. doi: 10.1007/s00424-010-0828-y. Epub 2010 Apr 16.
The plasma membrane phosphoinositide phosphatidylinositol 4,5-bisphosphate (PIP2) controls the activity of most ion channels tested thus far through direct electrostatic interactions. Mutations in channel proteins that change their apparent affinity to PIP2 can lead to channelopathies. Given the fundamental role that membrane phosphoinositides play in regulating channel activity, it is surprising that only a small number of channelopathies have been linked to phosphoinositides. This review proposes that for channels whose activity is PIP2-dependent and for which mutations can lead to channelopathies, the possibility that the mutations alter channel-PIP2 interactions ought to be tested. Similarly, diseases that are linked to disorders of the phosphoinositide pathway result in altered PIP2 levels. In such cases, it is proposed that the possibility for a concomitant dysregulation of channel activity also ought to be tested. The ever-growing list of ion channels whose activity depends on interactions with PIP2 promises to provide a mechanism by which defects on either the channel protein or the phosphoinositide levels can lead to disease.
质膜磷酸肌醇 4,5-二磷酸(PIP2)通过直接静电相互作用控制迄今为止测试的大多数离子通道的活性。改变通道蛋白对 PIP2 的表观亲和力的突变可导致通道病。鉴于膜磷酸肌醇在调节通道活性方面的基本作用,令人惊讶的是,只有少数通道病与磷酸肌醇有关。这篇综述提出,对于其活性依赖于 PIP2 的通道,并且对于那些突变可导致通道病的通道,应该测试这些突变是否改变了通道-PIP2 相互作用的可能性。同样,与磷酸肌醇途径紊乱相关的疾病会导致 PIP2 水平改变。在这种情况下,建议也应该测试通道活性同时失调的可能性。越来越多的离子通道的活性取决于与 PIP2 的相互作用,这为通道蛋白或磷酸肌醇水平的缺陷导致疾病提供了一种机制。