Somasekharan Suma, Brandt Robert, Iwamoto Takeo, Tomich John M, Schultz Bruce D
Yale School of Medicine Cellular and Molecular Physiology, New Haven, CT, USA.
J Membr Biol. 2008 Mar;222(1):17-30. doi: 10.1007/s00232-008-9099-3.
NC-1059 is a synthetic channel-forming peptide that provides for ion transport across, and transiently reduces the barrier integrity of, cultured epithelial monolayers derived from canine kidney (MDCK cells). Experiments were conducted to determine whether epithelial cells derived from other sources were similarly affected. Epithelial cells derived from human intestine (T-84), airway (Calu-3), porcine intestine (IPEC-J2) and reproductive duct (PVD9902) were grown on permeable supports. Basal short circuit current (Isc) was <3 microA cm(-2) for T-84, IPEC-J2 and PVD9902 cell monolayers and <8 microA cm(-2) for Calu-3 cells. Apical NC-1059 exposure caused, in all cell types, an increase in Isc to >15 microA cm(-2), indicative of net anion secretion or cation absorption, which was followed by an increase in transepithelial conductance (in mS cm(-2): T-84, 1.6 to 62; PVD9902, 0.2 to 51; IPEC-J2, 0.3 to 26; Calu-3, 2.3 to 13). These results are consistent with the peptide affecting transcellular ion movement, with a likely effect also on the paracellular route. NC-1059 exposure increased dextran permeation when compared to basal permeation, which documents an effect on the paracellular pathway. In order to evaluate membrane ion channels, experiments were conducted to study the dose dependence and stability of the NC-1059-induced membrane conductance in Xenopus laevis oocytes. NC-1059 induced a dose-dependent increase in oocyte membrane conductance that remained stable for greater than 2 h. The results demonstrate that NC-1059 increases transcellular conductance and paracellular permeation in a wide range of epithelia. These effects might be exploited to promote drug delivery across barrier epithelia.
NC - 1059是一种合成的通道形成肽,可促进离子穿过源自犬肾的培养上皮单层(MDCK细胞),并短暂降低其屏障完整性。进行实验以确定源自其他来源的上皮细胞是否受到类似影响。源自人肠道(T - 84)、气道(Calu - 3)、猪肠道(IPEC - J2)和生殖管道(PVD9902)的上皮细胞在可渗透支持物上生长。T - 84、IPEC - J2和PVD9902细胞单层的基础短路电流(Isc)<3微安/平方厘米,Calu - 3细胞的基础短路电流<8微安/平方厘米。顶端暴露于NC - 1059后,所有细胞类型的Isc均增加至>15微安/平方厘米,表明存在净阴离子分泌或阳离子吸收,随后跨上皮电导增加(以毫西门子/平方厘米计:T - 84,从1.6增至62;PVD9902,从0.2增至51;IPEC - J2,从0.3增至26;Calu - 3,从2.3增至13)。这些结果与该肽影响跨细胞离子运动一致,可能对细胞旁途径也有影响。与基础渗透相比,NC - 1059暴露增加了葡聚糖渗透,这证明了其对细胞旁途径的影响。为了评估膜离子通道,进行实验研究了NC - 1059诱导的非洲爪蟾卵母细胞膜电导的剂量依赖性和稳定性。NC - 1059诱导卵母细胞膜电导呈剂量依赖性增加,且在超过2小时内保持稳定。结果表明,NC - 1059可增加多种上皮细胞的跨细胞电导和细胞旁渗透。这些作用可用于促进药物跨屏障上皮的递送。