NEURAL LESIONING WITH RIBOSOME-INACTIVATING PROTEINS - SUICIDE TRANSPORT AND IMMUNOLESIONING

被引:166
作者
WILEY, RG
机构
[1] VET AFFAIRS MED CTR,NASHVILLE,TN 37212
[2] VANDERBILT UNIV,DEPT PHARMACOL,NASHVILLE,TN 37240
关键词
D O I
10.1016/0166-2236(92)90078-M
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Toxic lectins, plant proteins that inactivate ribosomes, irreversibly inhibit protein synthesis with high efficiency. After intraneural (subepineurial) microinjection, these agents are taken up by axons and are retrogradely transported to the perikarya, where they result in cell death. These 'suicide transport' toxins can produce pathway-specific lesions that are useful In several types of experiment, including cellular localization of neurotransmitter receptors. The toxins can be coupled to monoclonal antibodies to produce immunotoxin: reagents that can make highly selective lesions of specific types of neurons. Central or peripheral neurons that express the low-affinity NGF receptor are selectively destroyed by the immunotoxin 192 IgG-saporin. Development of other anti-neuronal immunotoxins should provide a variety of powerful selective lesioning tools.
引用
收藏
页码:285 / 290
页数:6
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