Liu Hao, Sun Qi, Ding Zheng, Shi Wensen, Wang Wen-Hui, Zhang Chengbiao
Department of Physiology, Xuzhou Medical University, Xuzhou, China.
Department of Pharmacology, New York Medical College, Valhalla, NY, United States.
Front Physiol. 2023 Aug 28;14:1242975. doi: 10.3389/fphys.2023.1242975. eCollection 2023.
The basolateral potassium channels play an important role in maintaining the membrane transport in the renal proximal tubules (PT) and adenosine receptors have been shown to regulate the trans-epithelial Na absorption in the PT. The aim of the present study is to explore whether adenosine also regulates the basolateral K channel of the PT and to determine the adenosine receptor type and the signaling pathway which mediates the effect of adenosine on the K channel. We have used the single channel recording to examine the basolateral K channel activity in the proximal tubules of the mouse kidney. All experiments were performed in cell-attached patches. Single channel recording has detected a 50 pS inwardly-rectifying K channel with high channel open probability and this 50 pS K channel is a predominant type K channel in the basolateral membrane of the mouse PT. Adding adenosine increased 50 pS K channel activity in cell-attached patches, defined by NP (a product of channel Numbers and Open Probability). The adenosine-induced stimulation of the 50 pS K channel was absent in the PT pretreated with DPCPX, a selective inhibitor of adenosine A1 receptor. In contrast, adenosine was still able to stimulate the 50 pS K channel in the PT pretreated with CP-66713, a selective adenosine A2 receptor antagonist. This suggests that the stimulatory effect of adenosine on the 50 pS K channel of the PT was mediated by adenosine-A1 receptor. Moreover, the effect of adenosine on the 50 pS K channel was blocked in the PT pretreated with U-73122 or Calphostin C, suggesting that adenosine-induced stimulation of the 50 pS K channels of the PT was due to the activation of phospholipase C (PLC) and protein kinase C (PKC) pathway. In contrast, the inhibition of phospholipase A2 (PLA2) with AACOCF3 or inhibition of protein kinase A (PKA) with H8 failed to block the adenosine-induced stimulation of the 50 pS K channel of the PT. We conclude that adenosine activates the 50 pS K channels in the basolateral membrane of PT via adenosine-A1 receptor. Furthermore, the effect of adenosine on the 50 pS K channel is mediated by PLC-PKC signaling pathway.
基底外侧钾通道在维持肾近端小管(PT)的膜转运中起重要作用,并且已表明腺苷受体可调节PT中的跨上皮钠吸收。本研究的目的是探讨腺苷是否也调节PT的基底外侧钾通道,并确定腺苷受体类型以及介导腺苷对钾通道作用的信号通路。我们使用单通道记录来检测小鼠肾脏近端小管中的基底外侧钾通道活性。所有实验均在细胞贴附式膜片上进行。单通道记录检测到一个50 pS内向整流钾通道,其通道开放概率高,并且这个50 pS钾通道是小鼠PT基底外侧膜中的主要钾通道类型。添加腺苷可增加细胞贴附式膜片中由NP(通道数量和开放概率的乘积)定义的50 pS钾通道活性。在用腺苷A1受体的选择性抑制剂DPCPX预处理的PT中,腺苷诱导的50 pS钾通道刺激消失。相反,在用选择性腺苷A2受体拮抗剂CP - 66713预处理的PT中,腺苷仍能够刺激50 pS钾通道。这表明腺苷对PT的50 pS钾通道的刺激作用是由腺苷A1受体介导的。此外,在用U - 73122或钙泊三醇C预处理的PT中,腺苷对50 pS钾通道的作用被阻断,这表明腺苷诱导的PT的50 pS钾通道刺激是由于磷脂酶C(PLC)和蛋白激酶C(PKC)途径的激活。相反,用AACOCF3抑制磷脂酶A2(PLA2)或用H8抑制蛋白激酶A(PKA)未能阻断腺苷诱导的PT的50 pS钾通道刺激。我们得出结论,腺苷通过腺苷A1受体激活PT基底外侧膜中的50 pS钾通道。此外,腺苷对50 pS钾通道的作用是由PLC - PKC信号通路介导的。