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4 - Cell birth and cell death in the central nervous system
- from PART I - INTRODUCTION AND GENERAL PRINCIPLES
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- By Samuel J. Pleasure, Department of Neurology University of California, San Francisco, David E. Pleasure, Departments of Neurology and Pediatrics Children's Hospital of Philadelphia
- Edited by Arthur K. Asbury, University of Pennsylvania School of Medicine, Guy M. McKhann, The Johns Hopkins University School of Medicine, W. Ian McDonald, University College London, Peter J. Goadsby, University College London, Justin C. McArthur, The Johns Hopkins University School of Medicine
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- Book:
- Diseases of the Nervous System
- Published online:
- 05 August 2016
- Print publication:
- 11 November 2002, pp 55-61
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- Chapter
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Summary
Formation of the neural tube and control of cell fate by dorsal–ventral signalling centres
One of the most remarkable features of mammalian neural development is the production of the complicated end product, the brain, spinal cord and peripheral nervous system, from a simple one-cell layer thick sheet of neuro-epithelial cells. The first step in this process is the formation and patterning of the neural tube through a process termed neural induction (Kandel et al., 2000). This involves the formation of a specialized region of columnar epithelium, called the neural plate, from the embryonic dorsal ectoderm. Soon after its formation the neural plate folds and becomes a tube (Fig. 4.1). In this process the most medial regions of the neural plate form the ventral neural tube and the more lateral regions of the neural plate form the dorsal neural tube. At the neural plate stage, signals from the mesoderm underlying it pattern the neural plate so that there are molecular differences between the rostral and caudal regions of the neural plate. Therefore, these early patterning events are fundamental to the later production of specialized regions and cells of the nervous system from the neural tube.
Neural induction is not completely understood at the molecular level but significant recent progress has been made (Harland, 2000). Current thinking is that the ectoderm at this stage of embryogenesis has a default neural fate except that the action of bone morphogenetic proteins (BMPs) and Wnts (a family of secreted glycoproteins similar to the wingless gene in Drosophila) expressed widely in the embryo suppress the acquisition of neural fate. Neural induction then occurs in the neural plate because of the release of soluble BMP and Wnt inhibitors from the underlying mesoderm. The inhibition of BMP and Wnt effects allows the default neural fate pathway to operate and the neural plate forms. The rostral–caudal patterning of the neural plate is further affected by the actions of molecules such as retinoic acid (which induces a caudal neural pattern).
After the neural tube forms, the rostral–caudal subdivisions (that will become the telencephalon, diencephalon, mesencephalon, metencephalon and spinal cord) become visible anatomically.
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