Logonder U, Jenko-Praznikar Z, Scott-Davey T, Pungercar J, Krizaj I, Harris J B
Department of Molecular and Biomedical Sciences, Jozef Stefan Institute, Ljubljana, Slovenia.
Exp Neurol. 2009 Oct;219(2):591-4. doi: 10.1016/j.expneurol.2009.07.017. Epub 2009 Jul 23.
A mutant form of ammodytoxin A, a neurotoxic phospholipase A(2) from the venom of the long nosed viper Vipera ammodytes ammodytes, was prepared by site-directed mutagenesis, conjugated to a nanogold particle and inoculated into the antero-lateral aspect of one hind limb of female mice. Eight hours later the mice were killed, the soleus muscles of both ipsi- and contra-lateral hind limbs were removed, exposed to a silver enhancing medium and then prepared for transmission electron microscopy. Silver-enhanced particles were subsequently found concentrated in the peri-synaptic area, particularly within the synaptic gutter and the deep synaptic folds, and in many cases had been taken up into the cytoplasm of the terminal boutons of the motor axon. The results suggest that the presynaptic neurotoxicity of snake venom phospholipases A(2) involves several components of the neuromuscular apparatus, including intracellular organelles of the motor nerve terminal.
通过定点诱变制备了长吻蝰蛇(Vipera ammodytes ammodytes)毒液中的神经毒性磷脂酶A₂——沙海蝰毒素A的一种突变形式,将其与纳米金颗粒偶联,并接种到雌性小鼠一侧后肢的前外侧。8小时后处死小鼠,切除同侧和对侧后肢的比目鱼肌,置于银增强介质中,然后制备用于透射电子显微镜观察的样本。随后发现银增强颗粒集中在突触周围区域,特别是在突触沟和深部突触褶皱内,并且在许多情况下已被摄取到运动轴突终末小体的细胞质中。结果表明,蛇毒磷脂酶A₂的突触前神经毒性涉及神经肌肉装置的几个组成部分,包括运动神经末梢的细胞内细胞器。