Wei Yuan, Wang Zhijian, Babilonia Elisa, Sterling Hyacinth, Sun Peng, Wang Wenhui
Dept. of Pharmacology, BSB Rm. 537, New York Medical College, Valhalla, NY 10595, USA.
Am J Physiol Renal Physiol. 2007 Apr;292(4):F1151-6. doi: 10.1152/ajprenal.00389.2006. Epub 2006 Dec 12.
We used the patch-clamp technique to study the effect of H(2)O(2) on the apical ROMK-like small-conductance K (SK) channel in the cortical collecting duct (CCD). The addition of H(2)O(2) decreased the activity of the SK channels and the inhibitory effect of H(2)O(2) was larger in the CCD from rats on a K-deficient diet than that from rats on a normal-K or a high-K diet. However, application of H(2)O(2) did not inhibit the SK channels in inside-out patches. This suggests that the H(2)O(2)-mediated inhibition of SK channels was not due to direct oxidation of the SK channel protein. Because a previous study showed that H(2)O(2) stimulated the expression of Src family protein tyrosine kinase (PTK) which inhibited SK channels (3), we explored the role of PTK in mediating the effect of H(2)O(2) on SK channels. The application of H(2)O(2) stimulated the activity of endogenous PTK in M-1 cells and increased tyrosine phosphorylation of ROMK in HEK293 cells transfected with GFP-ROMK1 and c-Src. However, blockade of PTK only attenuated but did not completely abolish the inhibitory effect of H(2)O(2) on SK channels. Since H(2)O(2) has also been demonstrated to activate mitogen-activated protein kinase, P38, and ERK (3), we examined the role of P38 and ERK in mediating the effect of H(2)O(2) on SK channels. Similar to blockade of PTK, suppression of P38 and ERK did not completely abolish the H(2)O(2)-induced inhibition of SK channels. However, combined use of ERK, P38, and PTK inhibitors completely abolished the effect of H(2)O(2) on SK channels. Also, treatment of the CCDs with concanavalin A, an agent which has been shown to inhibit endocytosis (19), abolished the inhibitory effect of H(2)O(2). We conclude that addition of H(2)O(2) inhibited SK channels by stimulating PTK activity, P38, and ERK in the CCD and that H(2)O(2) enhances the internalization of the SK channels.
我们采用膜片钳技术研究过氧化氢(H₂O₂)对皮质集合管(CCD)顶端类ROMK小电导钾(SK)通道的影响。添加H₂O₂可降低SK通道的活性,且与正常钾或高钾饮食的大鼠相比,缺钾饮食大鼠的CCD中H₂O₂的抑制作用更大。然而,在向外膜片上施加H₂O₂并不抑制SK通道。这表明H₂O₂介导的SK通道抑制并非由于SK通道蛋白的直接氧化。因为先前的一项研究表明H₂O₂可刺激Src家族蛋白酪氨酸激酶(PTK)的表达,而PTK会抑制SK通道(3),所以我们探究了PTK在介导H₂O₂对SK通道作用中的作用。施加H₂O₂可刺激M - 1细胞中内源性PTK的活性,并增加转染了GFP - ROMK1和c - Src的HEK293细胞中ROMK的酪氨酸磷酸化。然而,阻断PTK仅减弱但并未完全消除H₂O₂对SK通道的抑制作用。由于H₂O₂也已被证明可激活丝裂原活化蛋白激酶P38和ERK(3),所以我们研究了P38和ERK在介导H₂O₂对SK通道作用中的作用。与阻断PTK类似,抑制P38和ERK并未完全消除H₂O₂诱导的SK通道抑制。然而,联合使用ERK、P38和PTK抑制剂可完全消除H₂O₂对SK通道的作用。此外,用伴刀豆球蛋白A(一种已被证明可抑制内吞作用的试剂)处理CCD可消除H₂O₂的抑制作用。我们得出结论,添加H₂O₂通过刺激CCD中的PTK活性、P38和ERK来抑制SK通道,并且H₂O₂增强了SK通道的内化作用。