Forte L R, Eber S L, Turner J T, Freeman R H, Fok K F, Currie M G
Department of Pharmacology, Missouri University, Columbia 65212.
J Clin Invest. 1993 Jun;91(6):2423-8. doi: 10.1172/JCI116476.
Intestinal salt and fluid secretion is stimulated by Escherichia coli heat-stable enterotoxins (ST) through activation of a membrane guanylate cyclase found in the intestine. Guanylin is an endogenous intestinal peptide that has structural similarity to the bacterial peptides. Synthetic preparations of guanylin or E. coli ST 5-17 stimulated Cl- secretion in T84 cells cultured on semipermeable membranes as measured by increases in short circuit current (Isc). The guanylin/ST receptors appeared to be on the apical surface of T84 cells, since addition of guanylin to the apical, but not basolateral, reservoir stimulated Isc. Bumetanide added to the basolateral side effectively inhibited the Isc responses of T84 cells to either guanylin or ST 5-17. Guanylin appeared to be about one-tenth as potent as ST in stimulating transepithelial Cl- secretion. Guanylin and E. coli ST 5-17 both caused massive (> 1,000-fold) increases in cGMP levels in T84 cells, but guanylin was less potent than ST. Both peptides fully inhibited the binding of 125I-ST to receptor sites on intact T84 cells. The radioligand binding data obtained with guanylin or ST 5-17 best fit a model predicting two receptors with different affinity for these ligands. The Ki values for guanylin were 19 +/- 5 nM and 1.3 +/- 0.5 microM, whereas the Ki values for ST 5-17 were 78 +/- 38 pM and 4.9 +/- 1.4 nM. We conclude that guanylin stimulated Cl- secretion via the second messenger, cGMP, in T84 human colon cells. At least two guanylin receptors with different affinities for these ligands may exist in the cultured T84 cells. It may be postulated that guanylin is an endogenous hormone that controls intestinal Cl- secretion by a paracrine mechanism via cGMP and that E. coli ST stimulates Cl- secretion by virtue of an opportunistic mechanism through activation of guanylin receptors.
大肠杆菌热稳定肠毒素(ST)通过激活肠道中发现的一种膜鸟苷酸环化酶来刺激肠道盐分和液体分泌。鸟苷蛋白是一种内源性肠道肽,与细菌肽在结构上相似。如通过短路电流(Isc)增加所测量的,鸟苷蛋白或大肠杆菌ST 5 - 17的合成制剂刺激了在半透膜上培养的T84细胞中的氯离子分泌。鸟苷蛋白/ ST受体似乎位于T84细胞的顶端表面,因为将鸟苷蛋白添加到顶端储液器而非基底外侧储液器中会刺激Isc。添加到基底外侧的布美他尼有效地抑制了T84细胞对鸟苷蛋白或ST 5 - 17的Isc反应。在刺激跨上皮氯离子分泌方面,鸟苷蛋白的效力似乎约为ST的十分之一。鸟苷蛋白和大肠杆菌ST 5 - 17均导致T84细胞中cGMP水平大幅升高(> 1000倍),但鸟苷蛋白的效力低于ST。两种肽都完全抑制了125I - ST与完整T84细胞上受体位点的结合。用鸟苷蛋白或ST 5 - 17获得的放射性配体结合数据最符合预测对这些配体具有不同亲和力的两种受体的模型。鸟苷蛋白的Ki值为19±5 nM和1.3±0.5 μM,而ST 5 - 17的Ki值为78±38 pM和4.9±1.4 nM。我们得出结论,鸟苷蛋白在T84人结肠细胞中通过第二信使cGMP刺激氯离子分泌。在培养的T84细胞中可能存在至少两种对这些配体具有不同亲和力的鸟苷蛋白受体。可以推测,鸟苷蛋白是一种内源性激素,通过旁分泌机制经由cGMP控制肠道氯离子分泌,而大肠杆菌ST通过激活鸟苷蛋白受体凭借机会主义机制刺激氯离子分泌。