Vetter A E, Deachapunya C, O'Grady S M
Department of Veterinary PathoBiology, 295 Animal Science/Veterinary Medicine Building, University of Minnesota, St. Paul, Minnesota 55108, USA.
J Membr Biol. 1997 Nov 15;160(2):119-26. doi: 10.1007/s002329900301.
Previous studies in our laboratory have shown that Na absorption across the porcine endometrium is stimulated by PGF2alpha and cAMP-dependent activation of a barium-sensitive K channel located in the basolateral membrane of surface epithelial cells. In this study, we identify and characterize this basolateral, barium-sensitive K conductance. Porcine uterine tissues were mounted in Ussing chambers and bathed with KMeSO4 Ringer solution. Amphotericin B (70 microM) was added to the luminal solution to permeabilize the apical membrane and determine the current-voltage relationship of the basolateral K conductance after activation by 100 microM CPT-cAMP. An inwardly rectifying current was identified which possessed a reversal potential of -53 mV when standard Ringer solution was used to bathe the serosal surface. The K:Na selectivity ratio was calculated to be 12:1. Administration of 5 mM barium to the serosal solution completely inhibited the current activated by cAMP under these conditions. In addition to these experiments, amphotericin-perforated whole cell patch clamp recordings were obtained from primary cultures of porcine surface endometrial cells. The isolated cells displayed an inwardly rectifying current under basal conditions. This current was significantly stimulated by CPT-cAMP and blocked by barium. These results together with our previous studies demonstrate that cAMP increases Na absorption in porcine endometrial epithelial cells by activating an inwardly rectifying K channel present in the basolateral membrane. Similar patch clamp experiments were conducted using cells from a human endometrial epithelial cell line, RL95-2. An inwardly rectifying current was also identified in these cells which possessed a reversal potential of -56 mV when the cells were bathed in standard Ringer solution. This current was blocked by barium as well as cesium. However, the current from the human cells did not appear to be activated by cAMP, indicating that distinct subtypes of inwardly rectifying K channels are present in endometrial epithelial cells from different species.
我们实验室之前的研究表明,前列腺素F2α(PGF2α)和位于表面上皮细胞基底外侧膜的钡敏感钾通道的环磷酸腺苷(cAMP)依赖性激活可刺激猪子宫内膜对钠的吸收。在本研究中,我们鉴定并表征了这种基底外侧的、钡敏感的钾电导。将猪子宫组织安装在尤斯灌流小室中,并用硫酸钾林格溶液(KMeSO4 Ringer solution)进行灌流。向管腔溶液中加入两性霉素B(70微摩尔),使顶端膜通透,并在100微摩尔环磷腺苷-cAMP(CPT-cAMP)激活后测定基底外侧钾电导的电流-电压关系。鉴定出一种内向整流电流,当使用标准林格溶液灌流浆膜表面时,其反转电位为-53毫伏。计算得出钾与钠的选择性比率为12:1。在这些条件下,向浆膜溶液中加入5毫摩尔钡可完全抑制由cAMP激活的电流。除了这些实验外,还从猪表面子宫内膜细胞的原代培养物中获得了两性霉素穿孔全细胞膜片钳记录。分离的细胞在基础条件下显示出内向整流电流。该电流受到CPT-cAMP的显著刺激,并被钡阻断。这些结果与我们之前的研究共同表明,cAMP通过激活存在于基底外侧膜的内向整流钾通道来增加猪子宫内膜上皮细胞对钠的吸收。使用来自人子宫内膜上皮细胞系RL95-2的细胞进行了类似的膜片钳实验。在这些细胞中也鉴定出一种内向整流电流,当细胞在标准林格溶液中灌流时其反转电位为-56毫伏。该电流被钡以及铯阻断。然而,来自人细胞的电流似乎未被cAMP激活,表示不同物种的子宫内膜上皮细胞中存在内向整流钾通道的不同亚型。