Reznikov K Y
Central Scientific Research Laboratory, Medical Faculty, Patrice Lumumba Peoples' Friendship University, Moscow, USSR.
Adv Anat Embryol Cell Biol. 1991;122:1-74. doi: 10.1007/978-3-642-76447-9.
In the present work, processes of cell proliferation, cell death, neurogenesis, and gliogenesis in the mouse hippocampus were studied. The mapping of distribution of hippocampal mitoses and counting of their number allowed a more precise definition of the data concerning the disposition and age reduction of proliferative sites in Ammon's horn and the dentate gyrus in the mouse. As a result, the following generalized scheme of development and age reduction of the germinal zones in the mouse hippocampus has been suggested. 1. Ammon's horn a) The ventricular zone, from the beginning of formation of the hippocampus (E11) until E20 b) The suprafimbrial zone, from E16 until P7 2. Dentate gyrus a) The prime germinal zone ("the anlage of the dentate gyrus" of Stanfield and Cowan1979b), from E15 until P3 b) The proliferative zone of the hilus, from P3 until P14 c) The subgranular zone, from P3 until adult age The adduced scheme needs some comments: 1. In the hippocampus (as well as in other formations of the developing brain), primary precursors of all types of cells of neuroectodermal origin are represented by cells of the ventricular zone. They give rise to cells of secondary germinal zones in the dentate gyrus and Ammon's horn and are direct precursors of the majority (if not of all) neuronal cells in Ammon's horn, the earliest originating generations of neurons in the dentate gyrus, hippocampal radial glial cells, and, evidently, of a considerable part of astroblasts and oligodendroblasts in Ammon's horn. 2. In contrast to the subiculum, Ammon's horn in the mouse lacks a subventricular (subependymal) zone. These data differ from the results obtained in the rat, where the subventricular zone is described both in the subiculum and Ammon's horn (Bayer 1980b) and from the study in the monkey, where the subiculum and Ammon's horn lack the subventricular zone (Nowakowski and Rakic 1981). Thus, in the case of the mouse, the subventricular zone can serve as a cytoarchitectural characteristic allowing detection of a border between the developing subiculum and Ammon's horn. (Another developmental feature which also identifies the border between Ammon's horn and the subiculum is a considerable number of dying cells in the region of the joint of these structures on E20-P3). 3. In the developing dentate gyrus and Ammon's horn, several extraventricular (i.e., located at a distance from brain ventricles) secondary germinal zones exist. Thus, during embryonic and early postnatal periods of the mouse development, the prime germinal zone occupies a larger part of the presumptive dentate gyrus.(ABSTRACT TRUNCATED AT 400 WORDS)
在本研究中,对小鼠海马体中的细胞增殖、细胞死亡、神经发生和胶质细胞生成过程进行了研究。海马体有丝分裂分布的图谱绘制及其数量的计数,使得关于小鼠海马角和齿状回中增殖位点的分布和年龄减少的数据定义更加精确。结果,提出了以下小鼠海马体生发区发育和年龄减少的总体方案。1. 海马角 a) 脑室区,从海马体开始形成(胚胎第11天)直到胚胎第20天 b) 伞上区,从胚胎第16天直到出生后第7天 2. 齿状回 a) 原始生发区(Stanfield和Cowan1979b所述的“齿状回原基”),从胚胎第15天直到出生后第3天 b) 门区增殖区,从出生后第3天直到出生后第14天 c) 颗粒下区,从出生后第3天直到成年 所提出的方案需要一些说明:1. 在海马体(以及发育中的大脑的其他结构中),神经外胚层起源的所有类型细胞的主要前体由脑室区的细胞代表。它们产生齿状回和海马角中的次级生发区的细胞,并且是海马角中大多数(如果不是全部)神经元细胞、齿状回中最早起源的神经元世代、海马体放射状胶质细胞的直接前体,显然也是海马角中相当一部分成纤维细胞和少突胶质细胞的直接前体。2. 与下托不同,小鼠的海马角缺乏脑室下(室管膜下)区。这些数据与在大鼠中获得的结果不同,在大鼠中,下托和海马角都描述有脑室下区(Bayer 1980b),也与在猴子中的研究不同,在猴子中,下托和海马角缺乏脑室下区(Nowakowski和Rakic 1981)。因此,就小鼠而言,脑室下区可作为一种细胞结构特征,用于检测发育中的下托和海马角之间的边界。(另一个也可识别海马角和下托之间边界的发育特征是在胚胎第20天至出生后第3天这些结构连接处区域有大量死亡细胞)。3. 在发育中的齿状回和海马角中,存在几个脑室外(即位于距脑室一定距离处)的次级生发区。因此,在小鼠发育的胚胎期和出生后早期,原始生发区占据推定齿状回的较大部分。(摘要截断于400字)