Bittner M A, Holz R W
Department of Pharmacology, University of Michigan Medical School, Ann Arbor 48109-0626.
J Neurochem. 1988 Aug;51(2):451-6. doi: 10.1111/j.1471-4159.1988.tb01059.x.
Tetanus exotoxin inhibited Ca2+-dependent catecholamine secretion in a dose-dependent manner in digitonin-permeabilized chromaffin cells. The inhibition was specific for tetanus exotoxin and the B fragment of tetanus toxin; the C fragment had no effect. Inhibition required the introduction of toxin into the cell, and was not seen when intact cells were preincubated with the toxin or toxin fragments. The degree of inhibition was related to the length of preincubation with toxin, as well as the concentration of toxin used. A short preincubation with toxin was sufficient to inhibit secretion, and the continued presence of toxin in the incubation medium was not required during the incubation with Ca2+. The inhibition of secretion by tetanus toxin or the B fragment was not overcome with increasing Ca2+ concentrations. Tetanus toxin also inhibited catecholamine secretion enhanced by phorbol ester-induced activation of protein kinase C. Thus, the toxin or a proteolytic fragment of the toxin can enter digitonin-permeabilized cells to interact with a component of the Ca2+-dependent exocytotic pathway to inhibit secretion.
破伤风外毒素在洋地黄皂苷通透处理的嗜铬细胞中,以剂量依赖的方式抑制钙离子依赖的儿茶酚胺分泌。这种抑制作用对破伤风外毒素和破伤风毒素的B片段具有特异性;C片段没有作用。抑制作用需要将毒素导入细胞内,当完整细胞与毒素或毒素片段预孵育时则未观察到这种抑制现象。抑制程度与毒素预孵育的时间长短以及所用毒素的浓度有关。与毒素进行短时间预孵育就足以抑制分泌,在与钙离子孵育期间并不需要在孵育培养基中持续存在毒素。破伤风毒素或B片段对分泌的抑制作用不会随着钙离子浓度的增加而被克服。破伤风毒素还抑制了佛波酯诱导的蛋白激酶C激活所增强的儿茶酚胺分泌。因此,毒素或其蛋白水解片段能够进入洋地黄皂苷通透处理的细胞,与钙离子依赖的胞吐途径的一个组分相互作用以抑制分泌。