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德雷尔突变小鼠海马结构和小脑的细胞构筑异常

Cytoarchitectonic abnormalities in hippocampal formation and cerebellum of dreher mutant mouse.

作者信息

Sekiguchi M, Shimai K, Guo H, Nowakowski R S

机构信息

Department of Anatomy, Tokai University School of Medicine, Kanagawa, Japan.

出版信息

Brain Res Dev Brain Res. 1992 May 22;67(1):105-12. doi: 10.1016/0165-3806(92)90030-z.

DOI:10.1016/0165-3806(92)90030-z
PMID:1638738
Abstract

The laminated structures in the hippocampal formation and cerebellum of homozygous dreher mice were compared to their littermates and to C57BL/6J mice in Nissl- and myelin-stained preparations. In the dreher dentate gyrus, ectopic granule cells were situated in the molecular layer, and frequently there was either partial or complete absence of the infrapyramidal limb of the granule cell layer. In the dreher hippocampus, the cells of the pyramidal cell layer in area CA3 formed widely dispersed arrangements, and there were ectopically situated pyramidal cells in the stratum radiatum and stratum oriens. In the dreher cerebellum, 3 abnormal patterns were observed: (1) disruptions of foliation with normal cytoarchitectonic structure, (2) foliation with a mixture of normal laminated structure and abnormal laminated structure, and (3) almost complete absence of the cerebellum. In abnormal folia exhibiting the second or third pattern, islands consisting of agglomerations of both granule cells and Purkinje cells or just granule cells were observed. The neuronal heterotopias and cytoarchitectonic disorganization observed in the present study are apparently secondary to disruption of cell proliferation and neuronal migration produced directly or indirectly by the dreher mutation. In addition, the fact that the phenotypic abnormalities in homozygous dreher mice produces different abnormal morphologies in different specimens may be useful for analyzing the development of the hippocampal formation and cerebellum.

摘要

在尼氏染色和髓鞘染色的标本中,将纯合子德雷尔小鼠海马结构和小脑的分层结构与其同窝小鼠以及C57BL/6J小鼠进行比较。在德雷尔小鼠的齿状回中,异位颗粒细胞位于分子层,并且颗粒细胞层的锥体下臂常常部分或完全缺失。在德雷尔小鼠的海马中,CA3区锥体细胞层的细胞形成广泛分散的排列,并且在辐射层和原层中有异位的锥体细胞。在德雷尔小鼠的小脑中,观察到3种异常模式:(1)具有正常细胞构筑结构的叶状结构破坏,(2)具有正常分层结构和异常分层结构混合的叶状结构,以及(3)小脑几乎完全缺失。在表现出第二种或第三种模式的异常小叶中,观察到由颗粒细胞和浦肯野细胞或仅颗粒细胞聚集组成的岛。本研究中观察到的神经元异位和细胞构筑紊乱显然继发于德雷尔突变直接或间接导致的细胞增殖和神经元迁移破坏。此外,纯合子德雷尔小鼠的表型异常在不同标本中产生不同异常形态这一事实可能有助于分析海马结构和小脑的发育。

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