Dreyfus L A, Harville B, Howard D E, Shaban R, Beatty D M, Morris S J
Division of Cell Biology, University of Missouri, Kansas City 64110-2499.
Proc Natl Acad Sci U S A. 1993 Apr 15;90(8):3202-6. doi: 10.1073/pnas.90.8.3202.
The heat-stable enterotoxin B (STB) of Escherichia coli is a 48-amino acid extracellular peptide that induces rapid fluid accumulation in animal intestinal models. Unlike other E. coli enterotoxins that elicit cAMP or cGMP responses in the gut [heat-labile toxin (LT) and heat-stable toxin A (STA), respectively], STB induces fluid loss by an undefined mechanism that is independent of cyclic nucleotide elevation. Here we studied the effects of STB on intracellular calcium concentration ([Ca2+]i), another known mediator of intestinal ion and fluid movement. Ca2+ and pH measurements were performed on different cell types including Madin-Darby canine kidney (MDCK), HT-29/C1 intestinal epithelial cells, and primary rat pituitary cells. Ca2+ and pH determinations were performed by simultaneous real-time fluorescence imaging at four emission wavelengths. This allowed dual imaging of the Ca(2+)- and pH-specific ratio dyes (indo-1 and SNARF-1, respectively). STB treatment induced a dose-dependent increase in [Ca2+]i with virtually no effect on internal pH in all of the cell types tested. STB-mediated [Ca2+]i elevation was not inhibited by drugs that block voltage-gated Ca2+ channels including nitrendipine, verapamil (L-type), omega-conotoxin (N-type), and Ni2+ (T-type). The increase in [Ca2+]i was dependent on a source of extracellular Ca2+ and was not affected by prior treatment of MDCK cells with thapsigargin or cyclopiazonic acid, agents that deplete and block internal Ca2+ stores. In contrast to these results, somatostatin and pertussis toxin pretreatment of MDCK cells completely blocked the STB-induced increase in [Ca2+]i. Taken together, these data suggest that STB opens a GTP-binding regulatory protein-linked receptor-operated Ca2+ channel in the plasma membrane. The nature of the STB-sensitive Ca2+ channel is presently under investigation.
大肠杆菌的热稳定肠毒素B(STB)是一种由48个氨基酸组成的细胞外肽,可在动物肠道模型中诱导快速的液体蓄积。与其他在肠道中引发cAMP或cGMP反应的大肠杆菌肠毒素不同[分别为热不稳定毒素(LT)和热稳定毒素A(STA)],STB通过一种不明确的机制诱导液体流失,该机制独立于环核苷酸升高。在此,我们研究了STB对细胞内钙浓度([Ca2+]i)的影响,钙是另一种已知的肠道离子和液体运动介质。对包括Madin-Darby犬肾(MDCK)细胞、HT-29/C1肠上皮细胞和原代大鼠垂体细胞在内的不同细胞类型进行了Ca2+和pH测量。通过在四个发射波长下同时进行实时荧光成像来测定Ca2+和pH。这允许对Ca2+和pH特异性比率染料(分别为indo-1和SNARF-1)进行双重成像。在所有测试的细胞类型中,STB处理均诱导[Ca2+]i呈剂量依赖性增加,而对细胞内pH几乎没有影响。STB介导的[Ca2+]i升高不受阻断电压门控Ca2+通道的药物抑制,这些药物包括尼群地平、维拉帕米(L型)、ω-芋螺毒素(N型)和Ni2+(T型)。[Ca2+]i的增加依赖于细胞外Ca2+的来源,并且不受用毒胡萝卜素或环匹阿尼酸预处理MDCK细胞的影响,这两种药物可耗尽并阻断细胞内Ca2+储存。与这些结果相反,对MDCK细胞进行生长抑素和百日咳毒素预处理可完全阻断STB诱导的[Ca2+]i增加。综上所述,这些数据表明STB在质膜上打开了一个与GTP结合调节蛋白相关的受体操纵性Ca2+通道。目前正在研究STB敏感的Ca2+通道的性质。