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Journal ArticleDOI

Electron microscopic identification of three classes of oligodendrocytes and a preliminary study of their proliferative activity in the corpus callosum of young rats.

S. Mori, +1 more
- 01 May 1970 - 
- Vol. 139, Iss: 1, pp 1-29
TLDR
In recent electron microscope studies of the corpus callosum in male rats, some of the cells were identified as microglia by staining with the weak silver carbonate method of del Rio‐Hortega, and others as astrocytes by stains with the gold chloride sublimate method of Ramón y Cajal.
Abstract
In recent electron microscope studies of the corpus callosum in 60–80 gm male rats, some of the cells were identified as microglia by staining with the weak silver carbonate method of del Rio-Hortega, and others as astrocytes by staining with the gold chloride sublimate method of Ramon y Cajal. In the present work, the cells which did not belong in one of these two groups were examined in the light microscope using semithin sections stained with toluidine blue and in the electron microscope using thin sections stained with uranyl-lead. These cells make up a large, somewhat heterogeneous group, but they have a few common features: regular nucleus, cytoplasm rich in ribosomes and microtubules, and a variable number of narrow, non-branching fine processes of uniform diameter. Because of these features, the cells are all taken to be oligodendrocytes. Three classes may be described within this group of cells: (a) light oligodendrocytes, which are large cells with pale nucleus, a large nucleolus, a cytoplasm containing rather small organelles as well as many free ribosomes, and giving off numerous fine processes; they make up about 6% of the glial cells in the corpus callosum; and they undergo mitosis at a rapid rate; (b) medium-shade oligodendrocytes, which are somewhat smaller cells with moderately dense nucleus and cytoplasm, containing well developed organelles, and giving off a fair number of fine processes; they make up about a quarter of the glial cells; and they undergo mitosis at a moderate rate; (c) dark oligodendrocytes, which are even smaller cells with very dense nucleus and cytoplasm, containing a prominent Golgi and structures referred to as lamellar bodies, and giving off very few fine processes; these cells make up about 40% of the glial cells; they do not undergo mitosis and probably arise from divisions of medium oligodendrocytes.

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Citations
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Journal ArticleDOI

Biology of Oligodendrocyte and Myelin in the Mammalian Central Nervous System

TL;DR: This review deals with the recent progress related to the origin and differentiation of the oligodendrocytes, their relationships to other neural cells, and functional neuroglial interactions under physiological conditions and in demyelinating diseases.
Journal ArticleDOI

Cell death and control of cell survival in the oligodendrocyte lineage

TL;DR: It is shown that about 50% of oligodendrocytes normally die in the developing rat optic nerve, apparently as a result of a competition for limiting amounts of survival signals and that a requirement for survival signals is more general than previously thought.
Journal ArticleDOI

NG2-expressing glial progenitor cells: an abundant and widespread population of cycling cells in the adult rat CNS.

TL;DR: Using antibodies against NG2 it is shown that NG2 is expressed by a distinct cell population in the mature CNS with the homogeneous antigenic phenotype of oligodendrocyte progenitors, and it is suggested that the size of the oligodendedrocytes population may actually increase during adult life.
Journal ArticleDOI

Co-localization of NG2 proteoglycan and PDGF alpha-receptor on O2A progenitor cells in the developing rat brain.

TL;DR: Mapping experiments indicate that NG2‐positive, PDGF α‐receptor positive O2A cells are abundant throughout the developing central nervous system in both white and gray matter.
Journal ArticleDOI

Immunohistochemical localization of Ih channel subunits, HCN1-4, in the rat brain.

TL;DR: The results indicate that HCNs are localized not only in somato‐dendritic compartments but also in axonal compartments of neurons and further suggest unexpected roles of Ih channels in the brain.
References
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Journal ArticleDOI

Glial cells and the central myelin sheath.

R P Bunge
Journal ArticleDOI

Fixation of neural tissues for electron microscopy by perfusion with solutions of osmium tetroxide.

TL;DR: A method for obtaining nearly uniform fixation of the nervous system by vascular perfusion with solutions of osmium tetroxide is described and analysis of the structural relations between cells at the electron microscopic level to an extent that has not been possible heretofore.
Journal ArticleDOI

Identification of microglia in light and electron microscopy

TL;DR: The corpus callosum of male rats was processed by the weak silver carbonate method of del Rio‐Hortega for the detection of microglia and they were found to be a small nucleus in which dark chromatin contrasts with light nucleoplasm, and a cytoplasm containing dense bodies and poor in endoplasmic reticulum.
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