Kottra G
Zentrum der Physiologie, Johann Wolfgang Goethe-Universität, Frankfurt, Germany.
Pflugers Arch. 1995 Mar;429(5):647-58. doi: 10.1007/BF00373985.
The permeability properties of the forskolin-stimulated Cl- conductance in the apical membrane of Necturus gallbladder epithelium and the possible participation of intracellular Ca2+ in its stimulation have been investigated. The anion selectivity sequence as derived from biionic potential measurements (SCN- > I- approximately NO3- > Br- > Cl- >> ISE-) differed from the sequence derived from measurements of apical membrane resistance (NO3- approximately Br- approximately Cl- > SCN- > I- approximately ISE-). Accordingly, the conductance was inhibited by SCN- and I- which, from the potential measurements, appeared to be more permeable than Cl-. This finding agrees with observations of the cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channel reported recently. However, none of the commonly used Cl- channel blockers, such as 5-nitro-2-(3-phenylpropylamino)-benzoic acid (NPPB), 4,4'-diisothiocyanatostilbene-2,2'-disulphonic acid (DIDS), anthracene-9-carboxylic acid (9-AC) and glibenclamide reduced this conductance in Necturus gallbladder. In contrast to the situation in most other epithelia, elevation of intracellular Ca2+ concentration ([Ca2+]i) by ionomycin stimulated only K+ conductance and not that of Cl- in the apical cell membrane. Chelation of intracellular Ca2+ did not prevent the stimulation of Cl- conductance by forskolin. This indicates that [Ca2+]i does not have even a permissive role in the cyclic adenosine monophosphate-(cAMP)-mediated stimulation process, as would have been expected if exocytosis was involved. Further evidence against the involvement of exocytosis in the stimulation process came from the observation that the stimulation was not associated with an increase in apical membrane capacitance and was not suppressed by disruption of the cytoskeleton by preincubation of the tissue with cytochalasin D. The data indicate that Necturus gallbladder epithelium contains homologues of the CFTR Cl- channel which reside permanently in the apical cell membrane and which can be stimulated by a cAMP-dependent phosphorylation process without involvement of cell Ca2+ or exocytosis.
研究了无蹼螈胆囊上皮细胞顶端膜中福斯高林刺激的氯离子电导的通透性特性,以及细胞内钙离子在其刺激过程中可能的参与情况。通过双离子电位测量得出的阴离子选择性序列(SCN⁻>I⁻≈NO₃⁻>Br⁻>Cl⁻>>ISE⁻)与通过顶端膜电阻测量得出的序列(NO₃⁻≈Br⁻≈Cl⁻>SCN⁻>I⁻≈ISE⁻)不同。因此,SCN⁻和I⁻抑制了电导,从电位测量来看,它们似乎比Cl⁻更具通透性。这一发现与最近报道的囊性纤维化跨膜电导调节因子(CFTR)氯离子通道的观察结果一致。然而,常用的氯离子通道阻滞剂,如5-硝基-2-(3-苯丙基氨基)苯甲酸(NPPB)、4,4'-二异硫氰酸根合芪-2,2'-二磺酸(DIDS)、蒽-9-羧酸(9-AC)和格列本脲,均未降低无蹼螈胆囊的这种电导。与大多数其他上皮细胞的情况不同,离子霉素使细胞内钙离子浓度([Ca²⁺]i)升高,仅刺激了顶端细胞膜中的钾离子电导,而未刺激氯离子电导。细胞内钙离子的螯合并未阻止福斯高林对氯离子电导的刺激。这表明[Ca²⁺]i在环磷酸腺苷(cAMP)介导的刺激过程中甚至没有许可作用,而如果涉及胞吐作用,情况本应如此。反对胞吐作用参与刺激过程的进一步证据来自以下观察结果:刺激与顶端膜电容的增加无关,并且在组织用细胞松弛素D预孵育破坏细胞骨架后也未受到抑制。数据表明,无蹼螈胆囊上皮细胞含有CFTR氯离子通道的同源物,这些同源物永久存在于顶端细胞膜中,并且可以通过cAMP依赖的磷酸化过程被刺激,而不涉及细胞钙离子或胞吐作用。