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叙利亚仓鼠(金仓鼠)中细小病毒诱导的小脑发育不全的发病机制。荧光抗体、小脑叶片、细胞构筑、高尔基染色及电子显微镜研究。

The pathogenesis of parvovirus-induced cerebellar hypoplasia in the Syrian hamster, Mesocricetus auratus. Fluorescent antibody, foliation, cytoarchitectonic, Golgi and electron microscopic studies.

作者信息

Oster-Granite M L, Herndon R M

出版信息

J Comp Neurol. 1976 Oct 15;169(4):481-521. doi: 10.1002/cne.901690405.

Abstract

Cerebellar histogenesis was studied in hamsters infected at birth with a parvovirus, rat virus strain PRE 308. Cerebellar granule cell precursors in these animals were selectively infected and lysed in the external germinal layer before their migration to form the internal granular layer. The effects of the absence of granule cells on cerebellar development and especially on the development of the Purkinje cells and their dendrites was analyzed using fluorescent antibody. Golgi, conventional paraffin, and electron microscopic methods. This study represents the first Golgi and ultrastructural study of the pathogenesis of rat virus infections in the cerebellum. The destruction of the granule cell precursors resulted in a dysplastic cerebellar hypoplasia with total disruption of normal cerebellar stratification and cytoarchitectonics. The Purkinje cells developed misshapen, progressively disoriented dendritic stems lacking tertiary dendrites and studded with numerous spines, devoid of afferent synaptic contacts (naked spines) and encased by glial processes. These developmental studies, together with the mouse mutant studies, demonstrated that the spines of the Purkinje cells were elaborated in the absence of both tertiary dendrites and afferent parallel fiber contacts. Such data suggested that spine formation, once triggered, was intrinsically programmed rather than being dependent on the development of parallel fiber contacts. Despite the loss of a major interneuronal component and disintegration of normal cytoarchitectonic relationships, synapses in the cerebellar cortex developed normally as long as both the pre- and post-synaptic elements were present. Thus synaptic specificity is maintained in the face of gross disruption of cytoarchitectonic relationships. If either the pre- or post-synaptic portion of a contact was absent, then glial processes isolated the persisting element or aberrant contacts formed. In addition to glial encasement of naked spines, there were dendrodendritic articulations between Purkinje cell dendrites, some of which were joined by septate, plaque-like junctions. Aberrant synaptic contacts between mossy and climbing fiber glomeruli and the smooth surface of the Purkinje cell somata were found rarely. In addition to these contacts which also occur in the hypoplastic cerebella produced by other methods, previously undescribed non-synaptic spine-articulations between Purkinje cell dendrites were seen. The role played by granule cells and their axons in Purkinje cell development appeared to be two-fold. First, the development of the orderly array of parallel fibers in the normal animal played a role in orienting and flattening the dendritic trees of Purkinje cells. Second, the formation of tertiary dendritic branches appeared to depend primarily upon the presence of an external germinal layer throughout this stage of Purkinje cell development. By contrast, dendritic spines developed and persisted in the absence of granule cells.

摘要

对出生时感染细小病毒(大鼠病毒株PRE 308)的仓鼠的小脑组织发生进行了研究。这些动物的小脑颗粒细胞前体在迁移形成内颗粒层之前,在外颗粒层被选择性感染并裂解。使用荧光抗体、高尔基染色法、传统石蜡切片法和电子显微镜方法,分析了颗粒细胞缺失对小脑发育,尤其是对浦肯野细胞及其树突发育的影响。本研究是对大鼠病毒感染小脑发病机制的首次高尔基染色和超微结构研究。颗粒细胞前体的破坏导致发育异常的小脑发育不全,正常小脑分层和细胞构筑完全紊乱。浦肯野细胞发育出畸形、逐渐失去方向的树突干,缺乏三级树突,布满许多棘突,没有传入突触接触(裸棘),并被胶质细胞突起包裹。这些发育研究与小鼠突变体研究一起表明,浦肯野细胞的棘突在没有三级树突和传入平行纤维接触的情况下形成。这些数据表明,棘突形成一旦被触发,就是内在编程的,而不是依赖于平行纤维接触的发育。尽管失去了一个主要的中间神经元成分,正常的细胞构筑关系瓦解,但只要突触前和突触后成分都存在,小脑皮质中的突触就会正常发育。因此,在细胞构筑关系严重破坏的情况下仍能维持突触特异性。如果接触的突触前或突触后部分缺失,那么胶质细胞突起会隔离持续存在的成分或形成异常接触。除了裸棘被胶质细胞包裹外,浦肯野细胞树突之间还存在树突-树突连接,其中一些通过分隔的、斑块状连接相连。很少发现苔藓纤维和攀缘纤维小球与浦肯野细胞胞体光滑表面之间的异常突触接触。除了这些在其他方法产生的发育不全小脑中也会出现的接触外,还观察到了浦肯野细胞树突之间以前未描述的非突触棘突连接。颗粒细胞及其轴突在浦肯野细胞发育中所起的作用似乎有两个方面。首先,正常动物中平行纤维有序排列的发育在使浦肯野细胞的树突树定向和变平方面发挥了作用。其次,三级树突分支的形成似乎主要取决于在浦肯野细胞发育的整个阶段是否存在外颗粒层。相比之下,在没有颗粒细胞的情况下,树突棘仍能发育并持续存在。

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