Guo Y, Martinez-Williams C, Gilbert K A, Rannels D E
Department of Cellular and Molecular Physiology, The Pennsylvania State University College of Medicine, Hershey, Pennsylvania 17033, USA.
Am J Physiol. 1999 Jun;276(6):L1018-26. doi: 10.1152/ajplung.1999.276.6.L1018.
Cultured alveolar epithelial cells exhibit gap junction intercellular communication (GJIC) and express regulated levels of connexin (Cx) 43 mRNA and protein. Newly synthesized radiolabeled Cx43 protein equilibrates with phosphorylated Cx43 isoforms; these species assemble to form both connexons and functional gap junction plaques. The saponin 18alpha-glycyrrhetinic acid (GA) rapidly and reversibly blocks GJIC at low concentrations (5 microM). Extended exposure to 18alpha-GA at higher concentrations causes inhibition of GJIC and time- and dose-dependent reductions in both Cx43 protein and mRNA expression. The latter toxic effects are paralleled by disassembly of gap junction plaques and are reversed less readily than acute effects on GJIC. These observations demonstrate 18alpha-GA-sensitive regulation of intercellular communication in epithelial cells from the mammalian lung and suggest a role for Cx43 expression and phosphorylation in acute and chronic regulation of GJIC between alveolar epithelial cells.
培养的肺泡上皮细胞表现出间隙连接细胞间通讯(GJIC),并表达调节水平的连接蛋白(Cx)43 mRNA和蛋白。新合成的放射性标记的Cx43蛋白与磷酸化的Cx43亚型达到平衡;这些分子组装形成连接子和功能性间隙连接斑块。皂苷18α-甘草次酸(GA)在低浓度(5 microM)时能快速且可逆地阻断GJIC。在较高浓度下长时间暴露于18α-GA会导致GJIC受到抑制,并且Cx43蛋白和mRNA表达出现时间和剂量依赖性降低。后一种毒性作用伴随着间隙连接斑块的解体,并且比GJIC的急性作用更难逆转。这些观察结果证明了18α-GA对哺乳动物肺上皮细胞间通讯的敏感性调节,并表明Cx43表达和磷酸化在肺泡上皮细胞间GJIC的急性和慢性调节中发挥作用。