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成年小脑轴突再生中的内在特性和环境因素。

Intrinsic properties and environmental factors in the regeneration of adult cerebellar axons.

作者信息

Rossi F, Bravin M, Buffo A, Fronte M, Savio T, Strata P

机构信息

Department of Neuroscience, University of Turin, Italy.

出版信息

Prog Brain Res. 1997;114:283-96. doi: 10.1016/s0079-6123(08)63370-1.

Abstract

The success of axon regeneration in the adult mammalian brain depends on the presence of growth-permissive environmental conditions as well as on specific properties of the affected neurons. To investigate the relative contribution of extrinsic cues and intrinsic determinants to reparative processes we have investigated the regenerative properties of olivocerebellar and Purkinje cell axons. When these axon populations are severed in the cerebellar white matter and confronted with embryonic neural grafts of cerebellar or extracerebellar origin, the former vigorously regenerate into the transplant, whereas the latter invariably fail to do so (Rossi et al., 1995). The same response occurs when dissociated Schwann cells are implanted in the lesion site: Purkinje cell axons fail to regrow, whereas olivocerebellar fibres regenerate for considerable distances. Within the graft, regenerating fibres follow tortuous courses along Schwann cell bundles and sometimes end with poorly developed terminal plexuses. Some of them, however, succeed in crossing the graft and grow further into the host cortex, where they break into fine terminal branches confined to the granular layer. The remarkable regenerative response of olivocerebellar axons revealed by these experiments might be an intrinsic reaction of the affected neurons to axon injury or it might be elicited by growth promoting cues derived from the grafts. To elucidate this point we have undertaken the investigation of cellular changes occurring in adult inferior olivary neurons following the transection of the inferior cerebellar peduncle. Our results show that axotomy induces a series of cellular changes, or reparative and regressive character, which ultimately lead to cell death. Interestingly, however, these modifications are not uniformly distributed throughout the whole inferior olive. (i) Neuronal atrophy and degeneration progress more rapidly in the PO and DAO than in the MAO. (ii) A subpopulation of inferior olivary neurons become reactive for NADPH-diaphorase histochemistry, and their preferential localisation in the MAO suggests that this modification is related to the longer survival of these cells after axotomy. (iii) The developmentally regulated calcitonin gene-related peptide (CGRP) is reexpressed by a subset of neurons in the caudal nuclear compartments. These results further emphasise the conclusion that the dissimilar regenerative response of Purkinje cell and olivocerebellar axons confronted with permissive environmental conditions is due to different intrinsic properties of these neuronal populations. The reexpression of developmentally regulated substances by axotomised inferior olivary neurons suggests that their reparative reaction is triggered by axon injury. However, the pattern of growth of regenerating olivocerebellar axons is strongly conditioned by environmental constraints, which, in the present experimental conditions, do not allow them to reattain denervated Purkinje cells.

摘要

成年哺乳动物大脑中轴突再生的成功取决于生长允许性环境条件的存在以及受影响神经元的特定特性。为了研究外在线索和内在决定因素对修复过程的相对贡献,我们研究了橄榄小脑和浦肯野细胞轴突的再生特性。当这些轴突群体在小脑白质中被切断并与小脑或小脑外起源的胚胎神经移植物接触时,前者会有力地向移植物中再生,而后者则总是无法再生(Rossi等人,1995年)。当将解离的雪旺细胞植入损伤部位时,也会出现同样的反应:浦肯野细胞轴突无法再生,而橄榄小脑纤维则能再生相当长的距离。在移植物内,再生纤维沿着雪旺细胞束走曲折的路线,有时以发育不良的终末丛结束。然而,其中一些纤维成功穿过移植物并进一步向宿主皮质生长,在那里它们分成局限于颗粒层的细终末分支。这些实验揭示的橄榄小脑轴突显著的再生反应可能是受影响神经元对轴突损伤的内在反应,也可能是由移植物衍生的生长促进线索引发的。为了阐明这一点,我们对成年下橄榄核神经元在小脑下脚横断后发生的细胞变化进行了研究。我们的结果表明,轴突切断诱导了一系列具有修复和退行性特征的细胞变化,最终导致细胞死亡。然而,有趣的是,这些变化在整个下橄榄核中并非均匀分布。(i)PO和DAO中的神经元萎缩和退化比MAO中进展得更快。(ii)下橄榄核神经元的一个亚群对NADPH - 黄递酶组织化学呈反应性,它们在MAO中的优先定位表明这种变化与轴突切断后这些细胞的较长存活有关。(iii)发育调控的降钙素基因相关肽(CGRP)在尾侧核区的一部分神经元中重新表达。这些结果进一步强调了这样的结论,即面对允许性环境条件时,浦肯野细胞和橄榄小脑轴突不同的再生反应是由于这些神经元群体不同的内在特性。轴突切断的下橄榄核神经元中发育调控物质的重新表达表明它们的修复反应是由轴突损伤触发的。然而,再生的橄榄小脑轴突的生长模式受到环境限制的强烈制约,在目前的实验条件下,这些限制不允许它们重新连接到失神经支配的浦肯野细胞。

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