Prenatal gliogenesis in the neopallium of the rat
著者
書誌事項
Prenatal gliogenesis in the neopallium of the rat
（Advances in anatomy, embryology and cell biology, 93）
Springer-Verlag, c1985
- : gw
- : us
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注記
Bibliography: p. 94-102
Includes index
内容説明・目次
内容説明
At the end of the nineteenth century, controversy arose as to precisely when the first glial cells originate during development of the central nervous system, and to date, the issue has not been satisfactorily resolved. His (1889, 1890) noted that, even in the earliest developmental stages of the germinallayer, there appeared to be two distinct cell types. The cells which he called Spongioblasten were thought to be glial precursors from which all mature glial cells derive; Keimzellen, in contrast, were regarded as forming 1 neurons. His was working on the assumption that the very first preneurons migrate into a preexisting framework of glial eelIs. In contrast to this view, Schaper (1897) regarded both Keimzellen and Spongioblasten as belonging to a common population of proliferating and pluripotent stem cells which begin differentiation into glial and neuronal cells at late developmental stages. It is this latter view which is the basis of the most recent studies on the subject (e. g. , Caley and Maxwell1968a, 1968b; DeVitry et al. 1980).
The concept of one common stem cell seemed to be supported both by experiments using 3H-thymidine autoradiography (Fujita 1963, 1965b, 1966; Sauer and Walker 1959; Sidman et al. 1959) and by ultrastructural studies (Fu- jita 1966; Hinds and Ruffet 1971; Wechseler and Meller 1967) indicating that structural differences, which His presumably used to define his two cell types, could be related to different stages of the mitotic cycle.
目次
1 Introduction.- 1.1 Identification of Glial Cells.- 1.2 Histogenesis of the Neocortex.- 2 Material and Methods.- 2.1 Animals.- 2.2 Fixation.- 2.3 Standard Preparation of Tissues.- 2.4 Selection of Cortical Region for Analysis.- 2.5 3H-Thymidine Autoradiography.- 2.6 3H-GABA Autoradiography.- 2.7 Golgi Impregnation.- 2.8 Three-Dimensional Reconstructions of Electron Micrographs.- 2.9 Immunocytochemistry.- 2.10 Structural Criteria for Glial and Neuronal Cells.- 2.11 Text Structure and Terminology.- 3 Results.- 3.1 Histological Differentiation of the Neocortex.- 3.1.1 Early Marginal Zone (E13-E14).- 3.1.2 Late Marginal Zone (E15-E16).- 3.1.3 Subcortical Zone.- 3.1.4 Cortical Plate.- 3.1.5 Lamina I.- 3.1.6 Mesenchymal Structures.- 3.2 First Cells of the Marginal Zone.- 3.2.1 Shape of Cells at E14.- 3.2.2 Marginal Contact Cells.- 3.2.2.1 Pial End-feet.- 3.2.2.2 Perikaryon and Small Processes.- 3.2.3 Intercellular Contacts.- 3.3 Cells of Lamina I.- 3.3.1 Quiescent Presumptive Astrocytes (E 17-E 19).- 3.3.1.1 Perikaryon.- 3.3.1.2 Pial Process.- 3.3.2 Other Nonneuronal Cells (E17-E19).- 3.3.2.1 Dense Nucleus Cells.- 3.3.2.2 Intermediate Cells.- 3.3.3 Cells Containing GFAP and C1-Antigen (E18-E19).- 3.3.4 Distinction between Neuronal and Nonneuronal Cells.- 3.3.5 GABA-Accumulating Cells.- 3.3.6 Nonneuronal Cells at E 20 and E 21.- 3.4 Cells of the Deep Layers.- 3.4.1 Deep Marginal Zone (E15-E16).- 3.4.1.1 Polymorphic Cells and Mitotic Cells.- 3.4.1.2 Horizontal Neuron-like Cells.- 3.4.1.3 Cellular Processes.- 3.4.1.4 Intercellular Relations.- 3.4.2 Subcortical Zone (E 17-E 22).- 3.4.2.1 Dense Polymorphic Cells.- 3.4.2.2 Large Glial Precursors.- 3.4.2.3 Light Horizontal Cells.- 3.4.2.4 Phagocytes.- 3.4.2.5 Cell Proliferation.- 3.4.2.6 GABA Accumulation.- 3.4.2.7 Demonstration of GFAP and C1-Antigen (E 18, E 22).- 3.4.2.8 Golgi Impregnation.- 3.5 Nonneuronal Cells of the Cortical Plate.- 4 Discussion.- 4.1 Anlage of the Palliai Zones.- 4.2 Early Glial Cells with Pial Contact.- 4.3 Early Separation of Glial and Neuronal Cell Lines.- 4.4 Subcortical Cell Proliferation.- 4.5 Intercellular Contacts.- 4.6 Maturation of Glial Cells.- 4.7 Summary of Glial Criteria.- 5 Summary.- 6 References.- 7 Subject Index.
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