Arreola J, Melvin J E, Begenisich T
Department of Dental Research, University of Rochester Medical Center, New York 14642, USA.
Am J Physiol. 1998 Jan;274(1):C161-6. doi: 10.1152/ajpcell.1998.274.1.C161.
We investigated the regulation of Ca(2+)-activated Cl- channels in cells from the human colonic cell line T84 and acinar cells from rat parotid glands. The participation of multifunctional Ca(2+)- and calmodulin-dependent protein kinase (CaM kinase) II in the activation of these channels was studied using selective inhibitors of calmodulin and CaM kinase II. Ca(2+)-dependent Cl- currents were recorded using the whole cell patch-clamp technique. Direct inhibition of CaM kinase II by 40 microM peptide 281-302 or by 10 microM KN-62, another CaM kinase inhibitor, did not block the Cl- current in parotid acinar cells, whereas in T84 cells KN-62 markedly inhibited the Ca(2+)-dependent Cl- current. We also used the calmodulin-binding domain peptide 290-309 (0.5 microM), which competitively inhibits the activation of CaM kinase II. This peptide reduced the Cl- current in T84 cells by approximately 70% but was without effect on the channels in parotid acinar cells. We conclude that the Ca(2+)-dependent Cl- channels in T84 cells are activated by CaM kinase II but that the channels in parotid acinar cells must be regulated by a fundamentally different Ca(2+)-dependent mechanism that does not utilize CaM kinase II or any calmodulin-dependent process.
我们研究了人结肠癌细胞系T84细胞和大鼠腮腺腺泡细胞中钙激活氯离子通道的调节机制。使用钙调蛋白和钙调蛋白依赖性蛋白激酶(CaM激酶)II的选择性抑制剂,研究了多功能CaM激酶II在这些通道激活中的作用。采用全细胞膜片钳技术记录钙依赖性氯离子电流。用40微摩尔的肽281 - 302或10微摩尔的KN - 62(另一种CaM激酶抑制剂)直接抑制CaM激酶II,并未阻断腮腺腺泡细胞中的氯离子电流,而在T84细胞中,KN - 62显著抑制了钙依赖性氯离子电流。我们还使用了钙调蛋白结合域肽290 - 309(0.5微摩尔),它竞争性抑制CaM激酶II的激活。该肽使T84细胞中的氯离子电流降低了约70%,但对腮腺腺泡细胞中的通道没有影响。我们得出结论,T84细胞中的钙依赖性氯离子通道由CaM激酶II激活,但腮腺腺泡细胞中的通道必定受一种根本不同的钙依赖性机制调节,该机制不利用CaM激酶II或任何钙调蛋白依赖性过程。