Lawrence Gary W, Foran Patrick, Oliver Dolly J
Centre for Neurobiochemistry, Department of Biological Sciences, Imperial College of Science, Technology and Medicine, London, UK.
Toxicology. 2002 Dec 27;181-182:249-53. doi: 10.1016/s0300-483x(02)00453-5.
Inhibition of regulated exocytosis by botulinum toxins type A and B was studied in chromaffin cells. Both virtually abolished catecholamine release triggered from intact cells by depolarising stimuli, whereas the blockade by type A, but not B, was only partial after cell permeabilisation and direct stimulation of exocytosis by Ca(2+). Botulinum toxin A did not alter the [Ca(2+)]-dependency of exocytosis in permeabilised cells but, rather, proportionally reduced the amount of release at each concentration tested. Likewise, this toxin decreased the extents of Ca(2+)-induced structural changes in SNAP-25, synaptobrevin and syntaxin (known collectively as SNAREs), whilst leaving their [Ca(2+)]-sensitivity unaltered. Thus, botulinum toxin A does not reduce the Ca(2+)-sensitivity of the exocytosis sensor, but hinders transmission of the signal to the SNAREs which mediate fusion.
在嗜铬细胞中研究了A型和B型肉毒杆菌毒素对调节性胞吐作用的抑制作用。二者实际上都消除了去极化刺激引发的完整细胞中的儿茶酚胺释放,而在细胞透化并用Ca(2+)直接刺激胞吐作用后,A型毒素(而非B型毒素)的阻断作用仅为部分阻断。肉毒杆菌毒素A并未改变透化细胞中胞吐作用对[Ca(2+)]的依赖性,而是按比例降低了每个测试浓度下的释放量。同样,这种毒素减少了Ca(2+)诱导的SNAP-25、突触囊泡蛋白和 syntaxin(统称为SNAREs)结构变化的程度,同时使其对[Ca(2+)]的敏感性保持不变。因此,肉毒杆菌毒素A不会降低胞吐作用传感器对Ca(2+)的敏感性,而是会阻碍信号传递给介导融合的SNAREs。