Heckers S, Ohtake T, Wiley R G, Lappi D A, Geula C, Mesulam M M
Bullard Laboratory, Department of Neurology, Beth Israel Hospital, Boston, Massachusetts 02215.
J Neurosci. 1994 Mar;14(3 Pt 1):1271-89. doi: 10.1523/JNEUROSCI.14-03-01271.1994.
The immunotoxin 192 IgG-saporin, produced by coupling the ribosome-inactivating protein saporin to the monoclonal 192 IgG antibody against the low-affinity p75 NGF receptor (NGFr), was injected into the cerebral ventricle, septal area, and substantia innominata of adult rats. Injections into the cerebral ventricle induced a complete loss of NGFr-positive basal forebrain neurons and their axons. Extensive loss of cholinergic neurons was found in the septum, diagonal band, and magnocellular preoptic nucleus but not in the nucleus basalis-substantia innominata complex, where many cholinergic, presumably NGFr-negative, neurons remained intact. Cholinergic fibers were completely lost in the neocortex and hippocampus, showed some preservation in allocortical areas, and showed only minor loss in the amygdala. The NGFr-positive cholinergic basal forebrain neurons progressively degenerated during the first 5 d and did not recover after 180 d. The effect of intraventricular 192 IgG-saporin injections on NGFr-positive basal forebrain neurons could be blocked by simultaneous intraventricular injection of colchicine. Intraparenchymal injections into the septal area or substantia innominata damaged cholinergic neurons mainly around the injection sites and reduced their respective cortical and hippocampal projections. Noncholinergic septal neurons containing parvalbumin and noncholinergic neurons containing calbindin-D28k or NADPHd, which were adjacent to cholinergic nucleus basalis-substantia innominata neurons, were not affected by 192 IgG-saporin. The ChAT immunoreactivity in cortical interneurons, habenula, and brainstem was unchanged. Dopaminergic and noradrenergic cortical afferents remained intact. 192 IgG-saporin damaged two neuronal groups outside the basal forebrain that express the p75 NGF receptor: NGFr-positive cerebellar Purkinje cells after intraventricular injection and cholinergic striatal interneurons after injections into the substantia innominata. These results indicate that the immunotoxin 192 IgG-saporin induces a complete and selective lesion of NGFr-positive cholinergic basal forebrain neurons projecting to hippocampus and neocortex.
将核糖体失活蛋白皂草素与抗低亲和力p75神经营养因子受体(NGFr)的单克隆192 IgG抗体偶联产生的免疫毒素192 IgG-皂草素,被注射到成年大鼠的脑室、隔区和无名质中。向脑室注射导致NGFr阳性基底前脑神经元及其轴突完全丧失。在隔区、斜角带和视前大细胞核中发现胆碱能神经元大量丧失,但在基底核-无名质复合体中未发现,该复合体中有许多胆碱能神经元(推测为NGFr阴性)保持完整。胆碱能纤维在新皮层和海马中完全丧失,在旧皮层区域有一些保留,在杏仁核中仅轻微丧失。NGFr阳性胆碱能基底前脑神经元在最初5天内逐渐退化,180天后未恢复。脑室注射秋水仙碱可阻断脑室注射192 IgG-皂草素对NGFr阳性基底前脑神经元的影响。向隔区或无名质进行脑实质内注射主要损伤注射部位周围的胆碱能神经元,并减少它们各自向皮层和海马的投射。与胆碱能基底核-无名质神经元相邻的含有小白蛋白的非胆碱能隔区神经元以及含有钙结合蛋白-D28k或NADPHd的非胆碱能神经元,不受192 IgG-皂草素影响。皮层中间神经元、缰核和脑干中的ChAT免疫反应性未改变。多巴胺能和去甲肾上腺素能皮层传入纤维保持完整。192 IgG-皂草素损伤了基底前脑外两个表达p75 NGF受体的神经元群:脑室注射后NGFr阳性的小脑浦肯野细胞和注入无名质后胆碱能纹状体中间神经元。这些结果表明,免疫毒素192 IgG-皂草素可诱导投射至海马和新皮层的NGFr阳性胆碱能基底前脑神经元发生完全且选择性的损伤。