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[错位神经元与神经网络:reeler突变小鼠运动皮层的神经束路研究]

[Dislocated neurons and neural network: hodological study of the motor cortex of the reeler mutant mouse].

作者信息

Terashima T, Inoue K, Inoue Y

机构信息

Department of Anatomy, Hokkaido University School of Medicine, Sapporo, Japan.

出版信息

Hokkaido Igaku Zasshi. 1991 May;66(3):268-85.

PMID:1909294
Abstract

Reeler, an autosomal recessive mutation in mice, causes cytoarchitectonic abnormalities of cerebral cortex, which are characterized by malposition of neurons. We examined hodological systems of the reeler motor cortex. The results are described as follows. (1) In normal controls, corticospinal tract neurons retrogradely labeled after the injection of HRP ioto the lumbar cord were situated only in layer V (layer of large pyramids: LP). In the reeler, by contrast, the labeled corticospinal tract neurons were scattered diffusely throughout all levels of the corresponding area. (2) In the normal controls, callosal commissural neurons retrogradely labeled after the HRP injection into the motor cortex were distributed in a bilaminar pattern such that the largest number of cells were located in the supragranular layers II (layer of small pyramids; SP) and III (layer of medium pyramids; MP), and in the infragranular layer V (LP). In the reeler mutant mice, callosal commissural neurons were found in all cortical layers, but two-thirds were situated in the lower half of the cortex. (3) In the normal controls, most of the thalamocortical neurons labeled after HRP injection into the motor cortex were located in the ventrolateral nucleus, the lateral division of the ventrobasal nucleus, the central lateral, paracentral and central intralaminar nuclei, and the medial division of the posterior complex. In the reeler mutant mice, retrogradely labeled neurons were again found in the nuclei referred to above, and the distribution pattern and morphology of HRP-filled neurons were also similar to those of normal controls. In the reeler, thalamocortical fibers took an abnormal course within the motor cortex: they ascended obliquely from the white matter to the pial surface and then descended obliquely to the deeper layers. These results strongly suggest that dislocated neurons project correctly to normally-situated and/or abnormally situated target(s).

摘要

Reeler是小鼠中的一种常染色体隐性突变,会导致大脑皮质细胞结构异常,其特征为神经元位置错乱。我们研究了Reeler小鼠运动皮质的传导系统。结果如下:(1)在正常对照组中,将HRP注入腰髓后逆行标记的皮质脊髓束神经元仅位于第V层(大锥体层:LP)。相比之下,在Reeler小鼠中,标记的皮质脊髓束神经元分散分布在相应区域的所有层面。(2)在正常对照组中,将HRP注入运动皮质后逆行标记的胼胝体连合神经元呈双分层分布,即大多数细胞位于颗粒上层II(小锥体层;SP)和III(中锥体层;MP)以及颗粒下层V(LP)。在Reeler突变小鼠中,胼胝体连合神经元见于所有皮质层,但三分之二位于皮质下半部。(3)在正常对照组中,将HRP注入运动皮质后标记的大多数丘脑皮质神经元位于腹外侧核、腹基底核外侧部、中央外侧核、中央旁核和中央板内核以及后复合体内侧部。在Reeler突变小鼠中,再次在上述核团中发现逆行标记的神经元,且HRP填充神经元的分布模式和形态也与正常对照组相似。在Reeler小鼠中,丘脑皮质纤维在运动皮质内走行异常:它们从白质斜向上至软膜表面,然后斜向下至更深层。这些结果有力地表明,位置错乱的神经元能正确投射至正常位置和/或异常位置的靶标。

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