Pothoulakis C, Sullivan R, Melnick D A, Triadafilopoulos G, Gadenne A S, Meshulam T, LaMont J T
Section of Gastroenterology, Evans Memorial Department of Clinical Research, University Hospital, Boston, Massachusetts 02118.
J Clin Invest. 1988 Jun;81(6):1741-5. doi: 10.1172/JCI113514.
Clostridium difficile, a common enteric pathogen, mediates tissue damage and intestinal fluid secretion by release of two protein exotoxins: toxin A, an enterotoxin, and toxin B, a cytotoxin. Because toxin A elicits an intense inflammatory reaction in vivo, we studied the effects of highly purified C. difficile toxins on activation of human granulocytes. Toxin A at concentrations of 10(-7) to 10(-6) M, but not toxin B, elicited a significant chemotactic and chemokinetic response by granulocytes that was comparable with that induced by the chemotactic factor N-FMLP (10(-7) M). Neither toxin stimulated release of superoxide anion from granulocytes. Toxin A produced a rapid, transient rise in cytosolic [Ca2+]i, as measured by quin 2 fluorescence. Pertussis toxin and depletion of intra- and extracellular calcium blocked the toxin A effect on cytosolic [Ca2+]i. These findings suggest that the inflammatory effects of C. difficile toxin A in the intestine may be related to its ability to mobilize intracellular Ca2+ and elicit a chemotactic response by granulocytes.
艰难梭菌是一种常见的肠道病原体,通过释放两种蛋白质外毒素介导组织损伤和肠液分泌:毒素A,一种肠毒素;毒素B,一种细胞毒素。由于毒素A在体内引发强烈的炎症反应,我们研究了高度纯化的艰难梭菌毒素对人粒细胞激活的影响。浓度为10^(-7)至10^(-6) M的毒素A,而非毒素B,引发了粒细胞显著的趋化和化学动力学反应,该反应与趋化因子N - FMLP(10^(-7) M)诱导的反应相当。两种毒素均未刺激粒细胞释放超氧阴离子。通过喹啉2荧光测量,毒素A使胞质[Ca2+]i迅速短暂升高。百日咳毒素以及细胞内和细胞外钙的耗竭阻断了毒素A对胞质[Ca2+]i的影响。这些发现表明,艰难梭菌毒素A在肠道中的炎症作用可能与其动员细胞内Ca2+并引发粒细胞趋化反应的能力有关。