Abstract

The central nervous system areas displaying the highest structural and functional complexity correspond to the so called cortices, i.e., concentric alternating neuronal and fibrous layers. Corticogenesis, i.e., the development of the cortical organization, depends on the temporal-spatial organization of several developmental events: (a) the duration of the proliferative phase of the neuroepithelium, (b) the relative duration of symmetric (expansive) versus asymmetric (neuronogenic) sub phases, (c) the spatial organization of each kind of cell division, (e) the time of determination and cell cycle exit and (f) the time of onset of the post-mitotic neuronal migration and (g) the time of onset of the neuronal structural and functional differentiation. The first five events depend on molecular mechanisms that perform a fine tuning of the proliferative activity. Changes in any of them significantly influence the cortical size or volume (tangential expansion and radial thickness), morphology, architecture and also impact on neuritogenesis and synaptogenesis affecting the cortical wiring. This paper integrates information, obtained in several species, on the developmental roles of cell proliferation in the development of the optic tectum (OT) cortex, a multilayered associative area of the dorsal (alar) midbrain. The present review (1) compiles relevant information on the temporal and spatial organization of cell proliferation in different species (fish, amphibians, birds, and mammals), (2) revises the main molecular events involved in the isthmic organizer (IsO) determination and localization, (3) describes how the patterning installed by IsO is translated into spatially organized neural stem cell proliferation (i.e., by means of growth factors, receptors, transcription factors, signaling pathways, etc.) and (4) describes the morpho- and histogenetic effect of a spatially organized cell proliferation in the above mentioned species. A brief section on the OT evolution is also included. This section considers how the differential operation of cell proliferation could explain differences among species.

Highlights

  • The central nervous system areas displaying the highest structural and functional complexity correspond to the so called cortices, i.e., concentric alternating neuronal and fibrous layers

  • The present review (1) compiles relevant information on the temporal and spatial organization of cell proliferation in different species, (2) revises the main molecular events involved in the isthmic organizer (IsO) determination and localization, (3) describes how the patterning installed by IsO is translated into spatially organized neural stem cell proliferation and (4) describes the morpho- and histogenetic effect of a spatially organized cell proliferation in the above mentioned species

  • It is commonly considered that the simpler the central nervous system (CNS) organization the clearer is the relationship between the spatiotemporal organization of cell proliferation and morpho-histogenesis (Northcutt, 1983; Vanegas and Ito, 1983)

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Summary

BASIC ORGANIZATION OF THE DEVELOPING CENTRAL NERVOUS SYSTEM

The developing vertebrate central nervous system (CNS) is composed of distinct regions aligned along the cephaliccaudal (Cph-Cd) axis: Forebrain, Midbrain, Hindbrain, and Spinal Cord. Each prospective region is composed of two main populations of neural stem cells (NScs) characteristically located along the dorsal-ventral (Dor-Ven) axis: the alar (dorsal) and the basal (ventral) plates that originate associative and efferent neuronal populations, respectively. Cortices exhibit the highest structural and functional organization of the CNS. They receive afferent information from multiple origins, process and integrate the afferent information and elaborate complex responses

STRUCTURE AND FUNCTION OF THE MIDBRAIN TECTUM
Teleosts Fishes
Principal events
Most caudally
Temporal Regulation and Spatial Organization of Neural Stem Cell Proliferation
Maintaining the proliferative status Repression of neuronal differentiation
HYPOTHESIS ABOUT THE OPTIC TECTUM EVOLUTION
Findings
CONCLUDING REMARKS

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