Kawedia Jitesh D, Jiang Mengmeng, Kulkarni Amit, Waechter Holly E, Matlin Karl S, Pauletti Giovanni M, Menon Anil G
Department of Molecular Genetics, Biochemistry and Microbiology, University of Cincinnati College of Medicine, 231 Albert Sabin Way, Cincinnati, OH 45267-0524, USA.
J Pharmacol Exp Ther. 2008 Sep;326(3):829-37. doi: 10.1124/jpet.107.135798. Epub 2008 Jun 12.
Hg(2+) is commonly used as an inhibitor of many aquaporins during measurements of transcellular water transport. To investigate whether it could also act on the paracellular water transport pathway, we asked whether addition of Hg(2+) affected transport of radiolabeled probes through tight junctions of a salivary epithelial cell monolayer. Inclusion of 1 mM Hg(2+) decreased transepithelial electrical resistance by 8-fold and augmented mannitol and raffinose flux by 13-fold, which translated into an estimated 44% increase in pore radius at the tight junction. These Hg(2+)-induced effects could be partially blocked by the protein kinase A (PKA) inhibitor N-[2-((p-bromocinnamyl) amino) ethyl]-5-isoquinolinesulfonamide, 2HCl (H89), suggesting that both-PKA dependent and PKA-independent mechanisms contribute to tight junction regulation. Western blot analyses showed a 2-fold decrease in tight junction-associated occludin after Hg(2+) treatment and the presence of a novel hyperphosphorylated form of occludin in the cytoplasmic fraction. These findings were corroborated by confocal imaging. The results from this study reveal a novel contribution of the PKA pathway in Hg(2+)-induced regulation of tight junction permeability in the salivary epithelial barrier. Therapeutically, this could be explored for pharmacological intervention in the treatment of dry mouth, Sjögren's syndrome, and possibly other disorders of fluid transport.
在测量跨细胞水转运过程中,Hg(2+) 通常用作许多水通道蛋白的抑制剂。为了研究它是否也作用于细胞旁水转运途径,我们探究了添加 Hg(2+) 是否会影响放射性标记探针通过唾液上皮细胞单层紧密连接的转运。加入 1 mM Hg(2+) 使跨上皮电阻降低了 8 倍,并使甘露醇和棉子糖通量增加了 13 倍,这意味着紧密连接处的孔半径估计增加了 44%。这些 Hg(2+) 诱导的效应可被蛋白激酶 A(PKA)抑制剂 N-[2-((对溴肉桂基)氨基)乙基]-5-异喹啉磺酰胺二盐酸盐(H89)部分阻断,表明 PKA 依赖性和 PKA 非依赖性机制均参与紧密连接的调节。蛋白质印迹分析显示,Hg(2+) 处理后紧密连接相关的闭合蛋白减少了 2 倍,并且在细胞质部分存在一种新的超磷酸化形式的闭合蛋白。共聚焦成像证实了这些发现。本研究结果揭示了 PKA 途径在 Hg(2+) 诱导的唾液上皮屏障紧密连接通透性调节中的新作用。在治疗方面,这可为口干、干燥综合征以及可能的其他液体转运障碍的药物干预提供探索方向。