Early ganglion cell differentiation in the mouse retina: An electron microscopic analysis utilizing serial sections

The retina of a mouse embryo on day 13 of gestation, the first day when ganglion cells with axons are detectable, has been studied both qualitatively and quantitatively by reconstructing a large number of cells (more than 100) from an electron microscopic serial section series. Direct evidence has b...

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Veröffentlicht in:Developmental biology 1974-04, Vol.37 (2), p.381-416
Hauptverfasser: Hinds, James W., Hinds, Patricia L.
Format: Artikel
Sprache:eng
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Zusammenfassung:The retina of a mouse embryo on day 13 of gestation, the first day when ganglion cells with axons are detectable, has been studied both qualitatively and quantitatively by reconstructing a large number of cells (more than 100) from an electron microscopic serial section series. Direct evidence has been obtained for migration of prophase nuclei of ventricular cells to the ventricle within an intact process which spans the thickness of the retinal wall. At metaphase most of the vitreal process appears to be pinched off, and the cell completely rounds up. After cytokinesis, cells take one two courses: (1) regrowth of their vitreal process to the vitreal surface while keeping their ventricular process attached at the ventricular surface by a junctional complex; these cells will undergo another round of DNA synthesis and division; (2) regrowth of their vitreal process only so far as the marginal layer with detachment of their ventricular process from the junctional complex and beginning migration of their centrioles and cilium away from the ventricle. These changes represent the earliest detectable quantitative or qualitative changes undergone by cells that will subsequently differentiate into ganglion cells. The sequence of events for the formation of unipolar ganglion cells from these early bipolar cells involves transformation of the simple vitreal process ending in the marginal layer into an axonal growth cone insinuating itself between the tangential axons of the marginal layer and growing toward the optic stalk; at the same time the Golgi complex and centrioles migrate to the perikaryon, and the ventricular process completely withdraws. Usually, but not always, both daughter cells of a mitotic division appear to have the same fate, either both remain ventricular cells or both become ganglion cells. This result is used to construct a simple hypothesis explaining some of the apparently contradictory results of neuronal development, both in the retina and in the rest of the central nervous system.
ISSN:0012-1606
1095-564X
DOI:10.1016/0012-1606(74)90156-0