Department of Physiology, Iwate Medical University School of Medicine, 2-1-1 Nishitokuta, Yahaba 028-3694, Japan.
J Physiol Sci. 2013 Sep;63(5):377-87. doi: 10.1007/s12576-013-0275-6.
We investigated the effect of interleukin-1β (IL-1β) on activity of an inwardly rectifying K+ channel in cultured human proximal tubule cells (RPTECs), using the patch-clamp technique and Fura-2 Ca2+ imaging. IL-1β (15 pg/ml) acutely reduced K+ channel activity in cell-attached patches. This effect was blocked by the IL-1 receptor antagonist (20 ng/ml), an inhibitor of phospholipase C, neomycin (300 μM), and an inhibitor of protein kinase C (PKC), GF109203X (500 nM). The Fura-2 Ca2+ imaging revealed that IL-1β increased intracellular Ca2+ concentration even after removal of extracellular Ca2+, which was blocked by an inhibitor of inositol 1,4,5-trisphosphate receptors, 2-aminoethoxydiphenyl borate (2-APB, 1 μM). Moreover, IL-1β suppressed channel activity in the presence of 2-APB without extracellular Ca2+. These results suggest that IL-1β suppresses K+ channel activity in RPTECs through binding to its specific receptor and activation of the PKC pathway even though intracellular Ca2+ does not increase.
我们使用膜片钳技术和 Fura-2 Ca2+ 成像技术研究了白细胞介素-1β (IL-1β) 对培养的人近端肾小管细胞 (RPTEC) 内向整流型 K+ 通道活性的影响。IL-1β (15 pg/ml) 可急性降低细胞贴附式膜片钳中的 K+ 通道活性。这种作用被 IL-1 受体拮抗剂 (20 ng/ml)、磷脂酶 C 抑制剂 neomycin (300 μM) 和蛋白激酶 C (PKC) 抑制剂 GF109203X (500 nM) 阻断。Fura-2 Ca2+ 成像显示,IL-1β 可增加细胞内 Ca2+ 浓度,即使在去除细胞外 Ca2+ 后也是如此,这种作用被肌醇 1,4,5-三磷酸受体抑制剂 2-APB (1 μM) 阻断。此外,IL-1β 可在没有细胞外 Ca2+ 的情况下抑制 2-APB 存在时的通道活性。这些结果表明,IL-1β 通过与其特异性受体结合并激活 PKC 途径,即使细胞内 Ca2+ 不增加,也可抑制 RPTEC 中的 K+ 通道活性。