Translational Research Institute, Academic Health System, Hamad Medical Corporation, Doha, Qatar.
Biomed Res Int. 2020 Sep 9;2020:9692503. doi: 10.1155/2020/9692503. eCollection 2020.
Phosphoinositides play a regulatory role in clathrin-mediated endocytosis. However, their involvement in clathrin-independent endocytosis termed rapid endocytosis (RE), which is the mode of vesicle recycling during neurotransmitter release by transient fusion (known as kiss-and-run), has not been investigated. Here, we used patch-clamp recording of whole-cell membrane capacitance in adrenal chromaffin cells (ACC) to monitor changes of RE kinetics in response to pharmacological alteration of phosphatidylinositol-4,5-biphosphate (PI(4,5)P) level by phenylarsine oxide (PAO) or antibody against phosphatidylinositol 4-kinase (Ab).
We found that PAO and Ab significantly abrogated RE kinetics. Infusion of PI(4,5)P through the patch pipette potentiated RE kinetics and reversed PAO- and Ab-induced blockade of RE. Similarly, the application of the bifunctional thiol dithiothreitol (DTT) to PAO-treated cells completely prevented the inhibitory effect of PAO on RE. These findings indicate that PI(4,5)P is implicated in the signaling (mechanistic) process of RE in ACC.
磷酸肌醇在网格蛋白介导的胞吞作用中发挥调节作用。然而,它们在网格蛋白非依赖的胞吞作用(称为快速胞吞作用(RE))中的参与尚未被研究,这种胞吞作用是在神经递质释放过程中通过短暂融合(称为 kiss-and-run)进行囊泡再循环的方式。在这里,我们使用肾上腺嗜铬细胞(ACC)的全细胞膜电容的膜片钳记录来监测 RE 动力学的变化,以响应苯砷氧化物(PAO)或磷脂酰肌醇 4-激酶(PI4K)抗体对磷脂酰肌醇-4,5-二磷酸(PI(4,5)P)水平的药理学改变。
我们发现 PAO 和 Ab 显著消除了 RE 动力学。通过膜片钳内管输注 PI(4,5)P 增强了 RE 动力学,并逆转了 PAO 和 Ab 诱导的 RE 阻断。同样,将双功能硫醇二硫苏糖醇(DTT)应用于经 PAO 处理的细胞完全阻止了 PAO 对 RE 的抑制作用。这些发现表明,PI(4,5)P 参与了 ACC 中 RE 的信号(机制)过程。