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磷脂酶Cβ4的表达揭示了小脑拓扑结构在发育过程中的连续性。

Phospholipase Cbeta4 expression reveals the continuity of cerebellar topography through development.

作者信息

Marzban Hassan, Chung Seunghyuk, Watanabe Masahiko, Hawkes Richard

机构信息

Department of Cell Biology and Anatomy, Genes and Development Research Group, The University of Calgary, Calgary, Alberta T2N 4N1, Canada.

出版信息

J Comp Neurol. 2007 Jun 10;502(5):857-71. doi: 10.1002/cne.21352.

Abstract

Mediolateral boundaries divide the mouse cerebellar cortex into four transverse zones, and within each zone the cortex is further subdivided into a symmetrical array of parasagittal stripes. Various expression markers reveal this complexity, and detailed maps have been constructed based on the differential expression of zebrin II/aldolase C in a Purkinje cell subset. Recently, phospholipase (PL) Cbeta4 expression in adult mice was shown to be restricted to, and coextensive with, the zebrin II-immunonegative Purkinje cell subset. The Purkinje cell expression of PLCbeta4 during embryogenesis and postnatal development begins just before birth in a subset of Purkinje cells that are clustered to form a reproducible array of parasagittal stripes. Double label and serial section immunocytochemistry revealed that the early PLCbeta4-immunoreactive clusters in the neonate are complementary to those previously identified by neurogranin expression. The PLCbeta4 expression pattern can be traced continuously from embryo to adult, revealing the continuity of the topographical map from perinatal to adult cerebella. The only exception, as has been seen for other antigenic markers, is that transient PLCbeta4 expression (which subsequently disappears) is seen in some Purkinje cell stripes during the second postnatal week. Furthermore, the data confirm that some adult Purkinje cell stripes are composite in origin, being derived from two or more distinct embryonic clusters. Thus, the zone and stripe topography of the cerebellum is conserved from embryo to adult, confirming that the early- and late-antigenic markers share a common cerebellar topography.

摘要

中外侧边界将小鼠小脑皮质划分为四个横向区域,在每个区域内,皮质进一步细分为对称排列的矢状旁条纹。各种表达标记揭示了这种复杂性,并且已经基于zebrin II/醛缩酶C在浦肯野细胞亚群中的差异表达构建了详细的图谱。最近发现,成年小鼠中磷脂酶(PL)Cβ4的表达仅限于zebrin II免疫阴性的浦肯野细胞亚群,且与之共分布。胚胎期和出生后发育过程中浦肯野细胞中PLCβ4的表达在出生前就在一部分聚集形成可重复的矢状旁条纹阵列的浦肯野细胞中开始。双重标记和连续切片免疫细胞化学显示,新生儿中早期PLCβ4免疫反应性簇与先前通过神经颗粒素表达鉴定的簇互补。PLCβ4的表达模式可以从胚胎期一直追踪到成年期,揭示了从围产期到成年期小脑地形图的连续性。与其他抗原标记一样,唯一的例外是在出生后第二周,在一些浦肯野细胞条纹中可见短暂的PLCβ4表达(随后消失)。此外,数据证实一些成年浦肯野细胞条纹在起源上是复合的,源自两个或更多不同的胚胎簇。因此,小脑的区域和条纹地形从胚胎期到成年期都是保守的,这证实了早期和晚期抗原标记共享一个共同的小脑地形图。

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