Department of Brain Sciences, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu, 42988, Republic of Korea.
Neurovascular Unit Research Group, Korea Brain Research Institute (KBRI), Daegu, 41068, Republic of Korea.
Nat Commun. 2024 Aug 15;15(1):7008. doi: 10.1038/s41467-024-51400-y.
Proton-activated chloride (PAC) channels, ubiquitously expressed in tissues, regulate intracellular Cl levels and cell death following acidosis. However, molecular mechanisms and signaling pathways involved in PAC channel modulation are largely unknown. Herein, we determine that phosphatidylinositol 4,5-bisphosphate [PI(4,5)P] of the plasma membrane inner leaflet is essential for the proton activation of PAC channels. PI(4,5)P depletion by activating phosphatidylinositol 5-phosphatases or G protein-coupled muscarinic receptors substantially inhibits human PAC currents. In excised inside-out patches, PI(4,5)P application to the cytoplasmic side increases the currents. Structural simulation reveals that the putative PI(4,5)P-binding site is localized within the cytosol in resting state but shifts to the cell membrane's inner surface in an activated state and interacts with inner leaflet PI(4,5)P. Alanine neutralization of basic residues near the membrane-cytosol interface of the transmembrane helice 2 significantly attenuates PAC currents. Overall, our study uncovers a modulatory mechanism of PAC channel through inner membrane PI(4,5)P.
质子激活的氯离子 (PAC) 通道广泛表达于组织中,可调节细胞内 Cl-水平和酸中毒后的细胞死亡。然而,PAC 通道调节所涉及的分子机制和信号通路在很大程度上仍不清楚。本研究发现,质膜内层的磷脂酰肌醇 4,5-二磷酸 [PI(4,5)P] 对于 PAC 通道的质子激活是必需的。通过激活磷脂酰肌醇 5-磷酸酶或 G 蛋白偶联毒蕈碱受体来消耗 PI(4,5)P 会显著抑制人 PAC 电流。在分离的内面向外膜片中,PI(4,5)P 应用于细胞质侧会增加电流。结构模拟表明,假定的 PI(4,5)P 结合位点在静息状态下位于细胞质中,但在激活状态下会转移到细胞膜的内表面并与内叶 PI(4,5)P 相互作用。跨膜螺旋 2 中靠近膜-细胞质界面的碱性残基的丙氨酸中性化会显著减弱 PAC 电流。总体而言,本研究揭示了 PAC 通道通过内膜 PI(4,5)P 的调节机制。