New Experimental Trends for Phosphoinositides Research on Ion Transporter/Channel Regulation

Journal of Pharmacological Sciences

Masayuki X. Mori²  Ryuji Inoue¹ 

[1] Department of Physiology, School of Medicine, Fukuoka University, Japan;Department of Synthetic Chemistry and Biological Chemistry, School of Engineering, Kyoto University, Japan

关键词: phosphoinositide;    channel/transporter;    PI-turnover;    Ca2+ signal;    membrane lipid;   

DOI  :  10.1254/jphs.14R14CP

学科分类：药学

来源: Nihon Yakuri Gakkai Henshuubu / Japanese Pharmacological Society

【 摘 要 】

References(132)Cited-By(3)Phosphoinositides(4,5)-bisphosphates [PI(4,5)P2] critically controls membrane excitability, the disruption of which leads to pathophysiological states. PI(4,5)P2 plays a primary role in regulating the conduction and gating properties of ion channels/transporters, through electrostatic and hydrophobic interactions that allow direct associations. In recent years, the development of many molecular tools have brought deep insights into the mechanisms underlying PI(4,5)P2-mediated regulation. This review summarizes the methods currently available to manipulate the cell membrane PI(4,5)P2 level including pharmacological interventions as well as newly designed molecular tools. We concisely introduce materials and experimental designs suitable for the study of PI(4,5)P2-mediated regulation of ion-conducting molecules, in order to assist researchers who are interested in this area. It is our further hope that the knowledge introduced in this review will help to promote our understanding about the pathology of diseases such as cardiac arrhythmias, bipolar disorders, and Alzheimer’s disease which are somehow associated with a disruption of PI(4,5)P2 metabolism.

【 授权许可】

Unknown