Grunnet M, Knaus H G, Solander C, Klaerke D A
Department of Medical Physiology, The Panum Institute, University of Copenhagen, DK-2200 Copenhagen N, Denmark.
Am J Physiol. 1999 Jul;277(1):G22-30. doi: 10.1152/ajpgi.1999.277.1.G22.
The Ca(2+)-activated maxi K(+) channel is an abundant channel type in the distal colon epithelium, but nothing is known regarding the actual number and precise localization of these channels. The aim of this study has therefore been to quantify the maxi K(+) channels in colon epithelium by binding of iberiotoxin (IbTX), a selective peptidyl ligand for maxi K(+) channels. In isotope flux measurements 75% of the total K(+) channel activity in plasma membranes from distal colon epithelium is inhibited by IbTX (K(0.5) = 4.5 pM), indicating that the maxi K(+) channel is the predominant channel type in this epithelium. Consistent with the functional studies, the radiolabeled double mutant (125)I-IbTX-D19Y/Y36F binds to the colon epithelium membranes with an equilibrium dissociation constant of approximately 10 pM. The maximum receptor concentration values (in fmol/mg protein) for (125)I-IbTX-D19Y/Y36F binding to colon epithelium are 78 for surface membranes and 8 for crypt membranes, suggesting that the maxi K(+) channels are predominantly expressed in the Na(+)-absorbing surface cells, as compared with the Cl(-)-secreting crypt cells. However, aldosterone stimulation of this tissue induced by a low-Na(+) diet does not change the total number of maxi K(+) channels.
钙离子激活的大电导钾通道是远端结肠上皮中一种丰富的通道类型,但关于这些通道的实际数量和精确位置却一无所知。因此,本研究的目的是通过使用iberiotoxin(IbTX),一种大电导钾通道的选择性肽类配体,来定量结肠上皮中的大电导钾通道。在同位素通量测量中,IbTX(K(0.5)=4.5 pM)抑制了远端结肠上皮细胞膜中75%的总钾通道活性,这表明大电导钾通道是该上皮中的主要通道类型。与功能研究一致,放射性标记的双突变体(125)I-IbTX-D19Y/Y36F以约10 pM的平衡解离常数与结肠上皮细胞膜结合。(125)I-IbTX-D19Y/Y36F与结肠上皮结合的最大受体浓度值(以fmol/mg蛋白质计),表面膜为78,隐窝膜为8,这表明与分泌氯离子的隐窝细胞相比,大电导钾通道主要在吸收钠离子的表面细胞中表达。然而,低钠饮食诱导的醛固酮对该组织的刺激并没有改变大电导钾通道的总数。