Heming T A, Copello J, Reuss L
Department of Physiology, University of Texas Medical Branch, Galveston 77555.
J Gen Physiol. 1994 Jan;103(1):1-18. doi: 10.1085/jgp.103.1.1.
Regulation of the cAMP-activated apical membrane Cl- conductance (GaCl) in Necturus gallbladder (NGB) epithelial cells was investigated with intracellular-microelectrode techniques. GaCl was increased by exposure to 8-Br-cAMP, theophylline or forskolin. Neither 8-Br-cGMP nor elevation of intracellular [Ca2+] using ionomycin had effects on GaCl or interfered with activation of GaCl by forskolin. N-(2-[methylamino]ethyl)-5-isoquinolinesulfonamide (H8), an inhibitor of cAMP-dependent protein kinase (PKA), slowed but did not prevent the GaCl response to 8-Br-cAMP. Phorbol 12-myristate 13-acetate (PMA), which activates protein kinase C (PKC), stimulated GaCl but had no effects on intracellular [cAMP]. GaCl was unaffected by 4 alpha-phorbol, a PMA analog which does not activate PKC. Okadaic acid (OA), an inhibitor of protein phosphatases (PP) types 1 and 2A, slowed the activation of GaCl by 8-Br-cAMP, hastened the return of GaCl to basal values following removal of 8-Br-cAMP, and significantly reduced the elevation in intracellular [cAMP] produced by forskolin. OA had no effects on the GaCl changes elicited by theophylline. We conclude that: (a) NGB GaCl can be activated by PKA-mediated phosphorylation of apical membrane Cl- channels or a regulatory protein, (b) GaCl can also be activated via PKC, by a cAMP-independent mechanism, (c) OA-sensitive PP are not required for inactivation of GaCl; OA appears to stimulate phosphodiesterase, which lowers intracellular [cAMP] and affects GaCl activation, and (d) the apical membrane of NGB epithelium lacks a Ca(2+)-activated Cl- conductance.
采用细胞内微电极技术研究了美西螈胆囊(NGB)上皮细胞中环磷酸腺苷(cAMP)激活的顶膜氯离子电导(GaCl)的调节机制。暴露于8-溴-cAMP、茶碱或福斯高林可使GaCl增加。8-溴-cGMP或用离子霉素升高细胞内[Ca2+]对GaCl均无影响,也不干扰福斯高林对GaCl的激活作用。cAMP依赖性蛋白激酶(PKA)抑制剂N-(2-[甲氨基]乙基)-5-异喹啉磺酰胺(H8)可减缓但不能阻止GaCl对8-溴-cAMP的反应。激活蛋白激酶C(PKC)的佛波醇12-肉豆蔻酸酯13-乙酸酯(PMA)可刺激GaCl,但对细胞内[cAMP]无影响。不激活PKC的PMA类似物4α-佛波醇对GaCl无影响。蛋白磷酸酶(PP)1型和2A型抑制剂冈田酸(OA)可减缓8-溴-cAMP对GaCl的激活作用,加速去除8-溴-cAMP后GaCl恢复至基础值,并显著降低福斯高林引起的细胞内[cAMP]升高。OA对茶碱引起的GaCl变化无影响。我们得出以下结论:(a)NGB的GaCl可通过PKA介导的顶膜氯离子通道或调节蛋白的磷酸化被激活;(b)GaCl也可通过PKC以不依赖cAMP的机制被激活;(c)GaCl失活不需要OA敏感的PP;OA似乎刺激磷酸二酯酶,降低细胞内[cAMP]并影响GaCl激活;(d)NGB上皮细胞的顶膜缺乏Ca(2+)-激活的氯离子电导。