Sørensen J C, Castro A J, Klausen B, Zimmer J
PharmaBiotec, Institute of Neurobiology, University of Aarhus, Denmark.
Exp Brain Res. 1992;92(2):299-309. doi: 10.1007/BF00227972.
Fetal rat neocortex grafted into lesion cavities made in the newborn rat neocortex can exchange multiple axonal connections with the host brain. Most previous studies demonstrating efferent transplant-to-host brain connections have used fluorescent retrograde tracers injected into the host brain (Castro et al. 1985, 1987; Floeter and Jones 1984; O'Leary and Stanfield 1989). Other studies have used anterograde axonal tracing with either tritium-labelled amino acids impregnating the transplant and its efferents (Floeter and Jones 1985) or horseradish peroxidase injected into the transplants (Chang et al. 1984, 1986). In the present study we used the anterograde axonal tracer Phaseolus vulgaris-leucoagglutinin (PHA-L) to examine in detail the course and termination of the efferent neocortical graft fibers. Twenty-six newborn rats had the right frontal cortex forepaw area removed by vacuum aspiration, while anesthetized by hypothermia. A piece of fetal frontal cortex 14-16 embryonic days old (E14-16) was immediately thereafter placed in the lesion, and the recipient rats allowed to survive for 5-7 months. At this time the rats were reoperated under sodium pentobarbital (Nembutal) anesthesia and the transplants iontophoretically injected with PHA-L. Two weeks later the animals were again anesthetized, perfused, and processed for PHA-L immunocytochemistry and routine histology. Analysis of acetylcholinesterase- (AChE) and Nissl-stained sections showed graft survival in 19 of the 26 animals used in this study. When these 19 brains were processed for PHA-L immunocytochemistry, 5 of them were found with certainty to have the PHA-L injection confined to the transplant. Based on these cases PHA-L-reactive fibers arising from labelled transplant neurons were traced into the ipsilateral host neocortex adjacent to the transplant and found to project through the subcortical white matter to the ipsilateral parietal neocortical area 1, and claustrum. Callosal fibers were traced to the contralateral frontal neocortical forelimb and parietal areas. Transplant fibers were also observed to descend through the caudate putamen in the dispersed fiber bundles of the internal capsule to distribute as terminal branches and varicose fibers within the mesencephalic periaqueductal gray, red nucleus, deep mesencephalic nucleus, and intermediate gray of the superior colliculus, as well as in the pontine gray. Similar fibers and terminations were present in the caudate putamen, the reticular, ventrobasal, centrolateral, posterior, and parafascicular thalamic nuclei.(ABSTRACT TRUNCATED AT 400 WORDS)
移植到新生大鼠新皮质所形成的损伤腔内的胎鼠新皮质能够与宿主脑交换多条轴突连接。此前大多数证明移植组织与宿主脑之间存在传出连接的研究,都使用了注入宿主脑内的荧光逆行示踪剂(卡斯特罗等人,1985年、1987年;弗洛特和琼斯,1984年;奥利里和斯坦菲尔德,1989年)。其他研究则使用了顺行轴突追踪法,要么用氚标记的氨基酸浸染移植组织及其传出纤维(弗洛特和琼斯,1985年),要么将辣根过氧化物酶注入移植组织(张等人,1984年、1986年)。在本研究中,我们使用顺行轴突示踪剂菜豆白细胞凝集素(PHA-L)来详细研究传出性新皮质移植纤维的行程和终末。26只新生大鼠在低温麻醉下,通过真空抽吸去除右侧额叶皮质前爪区。此后立即将一块14 - 16胚胎日龄(E14 - 16)的胎鼠额叶皮质置于损伤处,受体大鼠存活5 - 7个月。此时,大鼠在戊巴比妥钠(Nembutal)麻醉下再次手术,通过离子导入法将PHA-L注入移植组织。两周后,再次麻醉动物,进行灌注,并进行PHA-L免疫细胞化学和常规组织学处理。对乙酰胆碱酯酶(AChE)和尼氏染色切片的分析显示,本研究中使用的26只动物中有19只移植组织存活。当对这19个脑进行PHA-L免疫细胞化学处理时,确定其中5个脑的PHA-L注射局限于移植组织。基于这些病例,追踪到来自标记移植神经元的PHA-L反应性纤维进入移植组织同侧相邻的宿主新皮质,并发现其通过皮质下白质投射到同侧顶叶新皮质1区和屏状核。胼胝体纤维追踪到对侧额叶新皮质前肢和顶叶区域。还观察到移植纤维通过内囊的分散纤维束下行穿过尾状壳核,作为终末分支和曲张纤维分布于中脑导水管周围灰质、红核、中脑深核以及上丘中间灰质,以及脑桥灰质中。类似的纤维和终末也存在于尾状壳核、丘脑网状核、腹基底核、中央外侧核、后核和束旁核中。(摘要截断于400字)