Suzuki M, Morita T, Hanaoka K, Kawaguchi Y, Sakai O
Second Department of Internal Medicine, Jikei University, Tokyo, Japan.
J Clin Invest. 1991 Sep;88(3):735-42. doi: 10.1172/JCI115370.
Previous data suggested an active Cl- conductance in the renal proximal convoluted tubule, although single channel conductance and regulation were not found. We have investigated the presence and regulation of the Cl- channel in proximal convoluted tubules by patch clamp analysis. The current-voltage relationship of whole cells with 130 mM NaCl in the pipette was nonlinear. The addition of 1-34 PTH (10(-8) M), forskolin, or cAMP significantly increased whole cell Cl- conductance. We found a single Cl- channel in excised apical membranes possessing conductance of 33 picosiemens (pS) at positive and 22.5 pS at negative potential, which was blocked by 4,4'-diisothiocyanostilbene-2,2'- disulfonic acid (10(-4) M) and was selective to Cl- (Cl/Na = 10). The channel was activated by prolonged membrane depolarization, by a catalytic subunit of protein kinase A (PKA), or by purified kinase C (PKC), but not by Ca2+ (1 microM) inside the membrane. During cell-attached patch clamping, the channel was similarly activated by PTH, phorbol ester, or dibutyryl cAMP in a dose-dependent manner. To investigate second messenger contributions to the PTH-action, the PTH-evoked channels were modified further by the subsequent addition of several blockers of the second messengers. This suggested that PKA and PKC were involved in Cl- channel activation. We therefore conclude that renal proximal convoluted tubule cells possess an apical Cl- channel activated by PTH via the PKA and PKC pathways.
先前的数据表明肾近端曲管中存在一种活跃的氯离子电导,尽管未发现单通道电导及其调节机制。我们通过膜片钳分析研究了近端曲管中氯离子通道的存在及其调节情况。移液管中含有130 mM氯化钠时,全细胞的电流-电压关系呈非线性。添加1-34甲状旁腺激素(10(-8) M)、福斯可林或环磷酸腺苷(cAMP)可显著增加全细胞氯离子电导。我们在切除的顶端膜中发现了一种单氯离子通道,在正电位下电导为33皮西门子(pS),负电位下为22.5 pS,该通道被4,4'-二异硫氰基芪-2,2'-二磺酸(10(-4) M)阻断,且对氯离子具有选择性(氯/钠 = 10)。该通道可通过长时间的膜去极化、蛋白激酶A(PKA)的催化亚基或纯化的蛋白激酶C(PKC)激活,但不受膜内钙离子(1 microM)的影响。在细胞贴附式膜片钳记录过程中,该通道同样可被甲状旁腺激素、佛波酯或二丁酰环磷酸腺苷以剂量依赖方式激活。为了研究第二信使对甲状旁腺激素作用的影响,在添加甲状旁腺激素诱发通道后,再添加几种第二信使阻滞剂对其进行进一步修饰。这表明PKA和PKC参与了氯离子通道的激活。因此,我们得出结论,肾近端曲管细胞具有一种顶端氯离子通道,该通道可通过PKA和PKC途径被甲状旁腺激素激活。