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首页> 外文期刊>Journal of chemical neuroanatomy >Development of the cerebellum in turbot ( Psetta maxima ): Analysis of cell proliferation and distribution of calcium binding proteins
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Development of the cerebellum in turbot ( Psetta maxima ): Analysis of cell proliferation and distribution of calcium binding proteins

机译:大菱岩中的小脑(Psetta Maxima)的发展:细胞增殖分析和钙结合蛋白的分布

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摘要

Highlights ? Metamorphosis is a critical period for differentiation of the turbot mature cerebellum. ? Ontogeny of neurons and cerebellar connectivity is evidenced by expression of CaBPs. ? Cytoarchitecture of proliferative zones may reflect inner migratory pathways in the cerebellum. Abstract The morphogenesis, cell proliferation and neuronal differentiation of the turbot ( Psetta maxima ) cerebellum has been studied using conventional histological techniques and immunohistochemical methods for proliferating cell nuclear antigen and calcium binding proteins. As in other vertebrates, the cerebellar anlage emerges as proliferative plates of neural tissue during the embryonic period. The anlage of the cerebellum persists without morphological changes until the end of the larval life when the mantle zone is differentiated. The major ontogenetic changesthat drive the formation of the cerebellar subdivisions begin in late premetamorphic larvae when cerebellar plates growth and merge medially. This transformation is accomplished by the reorganization of proliferative zones as well as by the onset of cell differentiation. The cerebellum becomes fully differentiated during metamorphosis when parvalbumin and calretinin were detected in Purkinje and eurydendroid cells. Sustained proliferation is maintained in all subdivisions of the cerebellum and this support the robust growth of this part of the brain that takes place during the metamorphic and juvenile periods.The location and histological organization of the proliferative activity in the turbot mature cerebellum are described and their functional significance was analyzed in light of the information available for other teleosts.
机译:强调 ?变态是轰鸣率成熟小脑分化的关键时期。还通过表达表达,神经元和小脑连接的组织发生和大脑连接。还增殖区的细胞建筑可以反映小脑中的内迁移途径。摘要使用常规的组织学技术和免疫组化方法研究了涡轮发动机(PSETTA Maxima)细胞的形态发生,细胞增殖和神经元分化,用于增殖细胞核抗原和钙结合蛋白。与其他脊椎动物一样,在胚胎周期期间,小脑窦形出现为神经组织的增殖板。小脑细胞的肾脏持续存在而不会发生形态变化,直到幼虫区分化时幼虫寿命结束。主要的OntogenceCency Mengesthat驱动器在晚期前一常晶的幼虫中开始形成小脑细胞的形成,当时小脑平板生长并在内侧合并。该转化是通过再组织增殖区以及细胞分化的开始来实现的。当在Purkinje和Eurydendroid细胞中检测到Parvalbumin和Calretinin时,细胞在变态期间变得完全分化。在小脑的所有细分中保持持续的增殖,这支持在变质和少年时期发生的大脑的这一部分的稳健生长。描述了涡蓝型成熟小脑中增殖活性的位置和组织学组织的位置和组织学组织根据可用的信息,分析了功能性意义。

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