Zagrebelsky M, Strata P, Hawkes R, Rossi F
Department of Neuroscience, University of Turin, Italy.
J Comp Neurol. 1997 Mar 10;379(2):283-99. doi: 10.1002/(sici)1096-9861(19970310)379:2<283::aid-cne9>3.0.co;2-#.
It is unclear whether reparative processes in the injured mammalian brain are able to restore the topographic organisation of neuronal connections. To address this question, we have investigated the plasticity of the olivocerebellar system. This pathway has a precise topographic arrangement, in which subsets of inferior olivary neurons project to parasagittally oriented Purkinje cell compartments. Following unilateral transection of the inferior cerebellar peduncle in newborn rats, axons from the contralateral projection cross the cerebellar midline and reinnervate the deafferented hemicerebellum. By this experimental approach, we first analysed the behaviour of calcitonin gene-related peptide (CGRP)-immunoreactive climbing fibres. This marker is transiently expressed by a subset of developing inferior olivary axons, which terminate in the cerebellar cortex into several parasagittal strips. We show that transcommissural axons reestablish the original pattern of climbing fibre bands within a few days after lesion. Then, in adult animals injured at birth, we assessed whether the newly formed climbing fibre bands align with zebrin II+/- Purkinje cell compartments, as in normal conditions. The newly formed projection is organised in parasagittally oriented strips which mirror the distribution of their counterparts on the intact side and are precisely aligned to the heterogeneous Purkinje cell compartments. In addition, the patchy distribution of olivo-nuclear fibres suggests that specific reinnervation is also achieved in the deep nuclei. Thus, transcommissural olivocerebellar reinnervation is not random, but it is regulated by selective interactions between distinct subsets of olivocerebellar axons and target neurons aimed at reestablishing the correct projection map.
目前尚不清楚受伤的哺乳动物大脑中的修复过程是否能够恢复神经元连接的拓扑组织。为了解决这个问题,我们研究了橄榄小脑系统的可塑性。这条通路具有精确的拓扑排列,其中下橄榄核神经元的子集投射到矢状旁定向的浦肯野细胞区室。在新生大鼠单侧横断小脑下脚后,来自对侧投射的轴突穿过小脑中线并重新支配去传入的半小脑。通过这种实验方法,我们首先分析了降钙素基因相关肽(CGRP)免疫反应性攀缘纤维的行为。该标记物由发育中的下橄榄核轴突的一个子集短暂表达,这些轴突在小脑皮质终止于几个矢状旁条带。我们发现,跨连合轴突在损伤后几天内重新建立了攀缘纤维带的原始模式。然后,在出生时受伤的成年动物中,我们评估了新形成的攀缘纤维带是否像在正常情况下一样与zebrin II+/-浦肯野细胞区室对齐。新形成的投射以矢状旁定向的条带形式组织,反映了其在完整侧对应物的分布,并与异质性浦肯野细胞区室精确对齐。此外,橄榄核纤维的斑片状分布表明,在深部核团中也实现了特异性的重新支配。因此,跨连合橄榄小脑重新支配不是随机的,而是由橄榄小脑轴突和靶神经元的不同子集之间的选择性相互作用调节的,目的是重新建立正确的投射图谱。