Guarino A, Cohen M, Thompson M, Dharmsathaphorn K, Giannella R
Department of Internal Medicine, Veterans Administration Hospital, Cincinnati 45220.
Am J Physiol. 1987 Dec;253(6 Pt 1):G775-80. doi: 10.1152/ajpgi.1987.253.6.G775.
Escherichia coli heat-stable enterotoxin (STa) induces intestinal secretion by binding to enterocyte receptors and activating the guanylate cyclase-guanosine 3',5'-cyclic monophosphate (cGMP) system. The intermediate steps between binding of STa and secretion are poorly understood, due in part to the lack of a convenient system to study the effects of STa at the cellular level. To establish such a model, we investigated the binding of 125I-STa, STa activation of guanylate cyclase, and STa-induced increase in cGMP production in a well-characterized human colonic cell line, T84. Binding was specific, linear with cell number, and time, temperature and pH dependent, and reversible. ST may also be internalized by these cells. Addition of unlabeled STa competitively inhibited binding of 125I-STa. These parameters closely resemble those described in intact rat enterocytes and cell-free membrane preparations. STa stimulated guanylate cyclase and cGMP production in a dose-related manner. The similar dose-response relationships for binding, guanylate cyclase stimulation by STa, and cGMP production suggest that the guanylate cyclase-cGMP system is coupled to ST occupancy of specific receptors. These data, together with the fact that STa induces chloride secretion from T84 cells suggest that T84 cells are a suitable and convenient system to study the cellular mechanism of action of STa.
大肠杆菌热稳定肠毒素(STa)通过与肠上皮细胞受体结合并激活鸟苷酸环化酶 - 鸟苷3',5'-环磷酸(cGMP)系统来诱导肠道分泌。由于缺乏一个方便的系统来在细胞水平研究STa的作用,STa结合与分泌之间的中间步骤目前了解甚少。为了建立这样一个模型,我们研究了125I-STa在一个特征明确的人结肠细胞系T84中的结合、STa对鸟苷酸环化酶的激活以及STa诱导的cGMP产生增加情况。结合具有特异性,与细胞数量呈线性关系,并且依赖时间、温度和pH值,且是可逆的。ST也可能被这些细胞内化。加入未标记的STa可竞争性抑制125I-STa的结合。这些参数与完整大鼠肠上皮细胞和无细胞细胞膜制剂中描述的参数非常相似。STa以剂量相关的方式刺激鸟苷酸环化酶和cGMP产生。结合、STa对鸟苷酸环化酶的刺激以及cGMP产生的相似剂量反应关系表明鸟苷酸环化酶 - cGMP系统与ST对特定受体的占据相关联。这些数据,连同STa诱导T84细胞氯离子分泌这一事实,表明T84细胞是研究STa细胞作用机制的一个合适且方便的系统。