Prenatal development of fibrous (white matter), protoplasmic (gray matter), and layer I astrocytes in the human cerebral cortex: A Golgi study
- 10 July 1995
- journal article
- research article
- Published by Wiley in Journal of Comparative Neurology
- Vol. 357 (4), 554-572
- https://doi.org/10.1002/cne.903570407
Abstract
The prenatal developmental histories of layer I, fibrous (white matter), and protoplasmic (gray matter) astrocytes have been studied in the human neocortex by the rapid Golgi method. The developmental route followed by each of these astrocytes is a distinct process which evolves from a specific precursor, occurs at a different time, and is linked to a specific event. The differentiation of layer I astrocytes is linked to the neocortex external glial limiting membrane (EGLM), that of fibrous astrocytes to the early white matter vascularization and maturation, and that of protoplasmic astrocytes to the late gray matter ascending vascularization and maturation. At the start of development, three glial precursors are established in the neocortex: 1) original radial neuroectodermal cells with nuclei above the primordial plexiform layer (PPL) by losing their ependymal and retaining their pial attachments become early astrocytes of layer I and EGLM components; 2) neuroectodermal cells with nuclei below the PPL that retain their pial and ependymal attachments become type I radial glial cells which are committed to the guidance of neurons and the early EGLM maintenance; and, 3) neuroectodermal cells that lose their pial but retain their ependymal attachment are transformed into type II radial glial precursors. By progressively losing their ependymal attachment, type II radial glia precursors become freely migrating cells, establish vascular contacts, and differentiate into fibrous astrocytes (and into oligodendrocytes?) throughout the subplate, developing white matter, and paraventricular regions. After the formation of the gray matter, additional layer I astrocytes are needed for the EGLM late prenatal and postnatal maintenance because type I radial glia cells start to regress and to reabsorb their EGLM endfeet. A late ependyma‐to‐pia migration of glial precursors progressively repopulates layer I with additional astrocytes and establishes the ephemeral subpial granular layer (SGL) of Ranke. From the 15th week of gestation to the time of birth, late astrocytes of layer I lose their EGLM attachments, migrate freely into the maturing gray matter, establish vascular contacts, and differentiate into protoplasmic astrocytes. The protoplasmic astrocytes of the gray matter evolve from transformation of layer I astrocytes rather than from radial glia cells as is generally believed.Keywords
This publication has 34 references indexed in Scilit:
- Organization of the embryonic and early postnatal murine hippocampus. I. Immunocytochemical characterization of neuronal populations in the subplate and marginal zoneJournal of Comparative Neurology, 1994
- Diverse Migratory Pathways tn the Developing Cerebral CortexScience, 1992
- The human transient subpial granular layer: An optical, immunohistochemical, and ultrastructural analysisJournal of Comparative Neurology, 1992
- The Germinative Zone Produces the Most Cortical Astrocytes after Neuronal Migration in the Developing Mammalian BrainNeonatology, 1992
- Three-dimensional structural organization of layer I of the human cerebral cortex: A golgi studyJournal of Comparative Neurology, 1990
- Neuron migration within the radial glial fiber system of the developing murine cerebrum: an electron microscopic autoradiographic analysisDevelopmental Brain Research, 1990
- Development of glial cells in the cerebral wall of ferrets: Direct tracing of their transformation from radial glia into astrocytesJournal of Comparative Neurology, 1989
- Early neurogenesis of the mouse olfactory nerve: Golgi and electron microscopic studiesJournal of Comparative Neurology, 1989
- Studies on the vasculogenesis in rat cerebral cortexThe Anatomical Record, 1989
- Transition between immature radial glia and mature astrocytes studied with a monoclonal antibody to vimentinDevelopmental Brain Research, 1984