Wictorin K, Isacson O, Fischer W, Nothias F, Peschanski M, Björklund A
Department of Medical Cell Research, University of Lund, Sweden.
Neuroscience. 1988 Nov;27(2):547-62. doi: 10.1016/0306-4522(88)90288-6.
Subcortical afferents to transplants of fetal striatal tissue, implanted into the excitotoxically lesioned striatum of adult recipient rats, were studied with retrograde and anterograde axonal tracers and immunohistochemistry. One week after a striatal ibotenic acid lesion, involving most of the head of the caudate-putamen, a suspension of fetal striatal tissue (embryonic day 14-15) was injected into the lesioned area. In one group of rats, the ibotenic acid lesion was preceded (10 days) by large intrastriatal injections of True Blue, with injection sites matching the area to be lesioned. This was done to retrogradely pre-label the host brain afferents to the area of the striatum later to be lesioned and grafted. At 3 or 6 months post-transplantation, small injections (50 nl) of rhodamine-labelled latex beads were made into the striatal grafts. In animals where the injections were confined to the graft, retrogradely labelled host brain neurons were found in the thalamus, the substantia nigra, amygdala and dorsal raphe nucleus. Double-labelling analysis revealed that the vast majority of the rhodamine bead-labelled neurons also contained True Blue, which indicates that the host afferents to the graft, to a large extent, were derived from the neurons which normally project to the area of the caudate-putamen which was lesioned by the ibotenic acid injection. To further substantiate these observations a second group of lesioned and grafted animals received unilateral wheatgerm agglutinin-horseradish peroxidase injections into the ipsilateral host thalamus at 4 months post-transplantation in order to anterogradely label the host thalamostriatal axons. In a third group of animals serotonin immunocytochemistry was performed in order to detect possible afferents from the raphe nuclei. In contrast to the serotonin-containing fibers, which were fairly evenly distributed throughout the graft tissue, the peroxidase-labelled thalamic afferents were most prominent in the peripheral zones of the grafts and they were densely aggregated at the graft-host interface. The combined results provide evidence that the intrastriatal grafts receive afferents from the host substantia nigra, thalamus, amygdala and dorsal raphe nucleus, but with different distributions. The afferents from the substantia nigra, amygdala and raphe nuclei seem to distribute throughout the grafted tissue, although they are most dense in the peripheral parts, whereas the thalamic afferents are largely confined to the peripheral areas of the transplants and to the graft-host interface.
将胎鼠纹状体组织移植到成年受体大鼠经兴奋性毒素损伤的纹状体中,运用逆行和顺行轴突示踪剂以及免疫组织化学方法,对其皮质下传入神经进行了研究。在用鹅膏蕈氨酸造成纹状体损伤(损伤累及尾壳核头部的大部分区域)一周后,将胎鼠纹状体组织悬液(胚胎第14 - 15天)注入损伤区域。在一组大鼠中,在注射鹅膏蕈氨酸造成损伤前10天,在纹状体内大量注射真蓝,注射部位与之后要损伤并移植的区域相对应。这样做是为了逆行预标记宿主脑内投射至之后将被损伤并移植的纹状体区域的传入神经。在移植后3或6个月,向纹状体移植物中微量注射(50纳升)罗丹明标记的乳胶微球。在注射局限于移植物的动物中,在丘脑、黑质、杏仁核和中缝背核中发现了逆行标记的宿主脑神经元。双重标记分析显示,绝大多数罗丹明微球标记的神经元也含有真蓝,这表明宿主至移植物的传入神经在很大程度上源自那些正常投射至因注射鹅膏蕈氨酸而损伤的尾壳核区域的神经元。为进一步证实这些观察结果,另一组损伤并移植的动物在移植后4个月接受了向同侧宿主丘脑单侧注射小麦胚凝集素 - 辣根过氧化物酶,以便顺行标记宿主丘脑纹状体轴突。在第三组动物中进行了5-羟色胺免疫细胞化学检测,以检测可能来自中缝核的传入神经。与在整个移植物组织中分布较为均匀的含5-羟色胺纤维不同,过氧化物酶标记的丘脑传入神经在移植物的周边区域最为明显,并且它们密集地聚集在移植物与宿主的界面处。综合结果表明,纹状体内移植物接受来自宿主黑质、丘脑、杏仁核和中缝背核的传入神经,但分布不同。来自黑质、杏仁核和中缝核的传入神经似乎分布于整个移植组织,尽管在周边部分最为密集,而丘脑传入神经主要局限于移植物的周边区域以及移植物与宿主的界面处。