Wiener H, Turnheim K
Department of Pharmacology, University of Vienna.
Wien Klin Wochenschr. 1990 Oct 26;102(20):622-8.
Using differential sedimentation, isopycnic and Ficoll-400 barrier centrifugation, basolateral membrane vesicles of surface and crypt cells of the rabbit distal colon were enriched 34- and 9-fold, respectively. 86Rb(+)-uptake into these vesicles, driven by an electrical potential difference, was stimulated by submicromolar Ca2+ activities and inhibited by Ba2+. These findings indicate the presence of Ca2(+)-activated K+ channels. The K+ channels in surface and crypt cell membranes differed with respect to inhibition by the bee venom apamin, the scorpion venom charybdotoxin and tetraethylammonium and exhibited a different pH dependence. Fusion of basolateral membrane vesicles with planar phospholipid bilayers revealed the presence of high-conductance Ba2(+)-sensitive K+ channels which were activated by micromolar Ca2+ and inhibited by crude scorpion venom and trifluoperazine. These K+ channels may be involved in the coupling of apical and basolateral membrane conductances during Na+ absorption and Cl- secretion, but they may also play a role in cell volume regulation.
利用差速沉降、等密度离心和Ficoll - 400梯度离心法,兔远端结肠表面细胞和隐窝细胞的基底外侧膜囊泡分别富集了34倍和9倍。由电位差驱动的86Rb(+)摄取进入这些囊泡,受到亚微摩尔浓度Ca2+活性的刺激,并被Ba2+抑制。这些发现表明存在Ca2(+)激活的K+通道。表面细胞膜和隐窝细胞膜中的K+通道在被蜂毒蜂毒明肽、蝎毒查卡毒素和四乙铵抑制方面存在差异,并且表现出不同的pH依赖性。基底外侧膜囊泡与平面磷脂双层的融合显示存在高电导的Ba2(+)敏感K+通道,这些通道被微摩尔浓度的Ca2+激活,并被粗制蝎毒和三氟拉嗪抑制。这些K+通道可能参与Na+吸收和Cl-分泌过程中顶端膜和基底外侧膜电导的偶联,但它们也可能在细胞体积调节中发挥作用。