Cell death in the developing chick optic tectum

The degeneration and death of early developing neuroblasts in the optic tectum of chick embryo during normal development have been investigated by electron microscopy.     

Involvement of the optic tectum and mesencephalic reticular formation in the generation of saccadic eye movements in goldfish

The circuitry and physiological properties underlying saccadic eye movement generation have been studied mainly in monkeys and cats. By contrast, current knowledge in nonmammalian species is rather scarce. We review here some of our recent findings about the involvement of the optic tectum and mesencephalic reticular formation in the generation of saccades in goldfish. Electrical microstimulation of the optic tectum evokes contraversive saccadic eye movements. In goldfish, as in mammals, the amplitude and direction of saccades are encoded in a spatial topographical map. In addition, there are some areas that have evolved, such as the extreme anteromedial tectal zone, whose activation yields eye convergence. Injections of the bidirectional tracer biotin dextran amine within functionally identified sites of the tectum provide reciprocal, site-dependent connectivity with different downstream structures. Of these structures, the major tectofugal target is the mesencephalic reticular formation. In goldfish, as in mammals, the mesencephalic reticular formation and optic tectum establish reciprocal connections at regional and neuronal levels which support the presence of feedback circuits. Electrical microstimulation demonstrates that the mesencephalic reticular formation can be functionally parceled—the rostral part is linked to vertical saccades, while the caudal part is related with horizontal ones. Finally, these zones are also differently connected to the optic tectum. From these data, we conclude that the involvement of the optic tectum and mesencephalic reticular formation in eye movement generation in goldfish is similar to that reported in cats and monkeys.     

Late developmental expression of DARPP-32 in the chick optic tectum

Immunohistochemical techniques reveal that the dopamine- and cAMP-regulated phosphoprotein DARPP-32 is detectable in neurons of the chick optic tectum starting on embryonic day 13. The expression levels then increase steadily from embryonic day 15 through the first posthatching day. After 15 days posthatching, expression of DARPP-32 reaches the adult pattern, with many labeled cells in tectal layers 11 and 12. These cells exhibit a bipolar shape, with long processes directed both to the deep and superficial layers. These results suggest that DARPP-32 is present in specific neuronal populations of the chick tectum and that this protein may not have a function in early ontogenetic processes.     

Arrested development of myelin in chick optic tectum following deaferrentation

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The levels of both an enzyme associated with myelin (2′,3′-cyclic nucleotide 3′-phosphohydrolase) and of a lipid constituent of myelin (galactocerebrosides) rise markedly in the chick optic lobe during the maturation of the newly hatched bird.     

Laminar redistribution of a glial subtype in the chick optic tectum.

Lamination is a central feature of structural organization and segregation within the central nervous system. Afferent fibers typically restrict their synapses to only one or a few specific laminae in the target region. Astroglial cells act as boundary markers for functional segregation of inputs in somatosensory cortex and the olfactory bulb and might also help to segregate particular connections in the neostriatum. This work presents evidence that a subset of astroglial cells expressing the carbohydrate recognized by tomato lectin are enriched in retino-non-recipient laminae of the chick optic tectum. This segregation is dependent upon retinal innervation; enucleated chick tecta contain cells that bind tomato lectin but do not segregate into their normal laminae. These results suggest that tomato lectin positive astrocytes of the superficial chick tectum play a role in defining or restricting lamina specific connections of retinal axons.     

Selective cultivation of N-cadherin expressing cells from the optic tectum of the chick

Dissociated primary cell cultures of the nervous system are usually composed of many different cell types, which makes it difficult to investigate a specific cell type and to describe its development in vitro without direct or indirect influence of other cell types. Although various methods have been published to specifically separate either neurons or glial cells, there is still a need for simple protocols to isolate distinct neuronal subpopulations. Here we describe a method to purify specific neuronal subtypes from the chick embryonic midbrain. Embryonic (E10) optic tecta were dissociated and a cell suspension was produced. Cells were separated by magnetic cell sorting (MACS) based on their specific expression of somatic N-cadherin. After cultivation on poly-D-lysine coated dishes in serum-free culture medium supplemented with B27, cells were fixed and analyzed with immuncytochemistry. Enriched primary cultures contained about 70% of N-cadherin positive cells compared to 46% before sorting. 7 days after cultivation, N-cadherin expression and its co-localization with synapses was demonstrated.     

Blood vessel ultrastructure in the chick optic tectum developing under chronic hypoxia conditions

Summary The maturation process of blood vessels has been ultrastructurally investigated in the optic tectum of chick embryos kept in a condition of aerogenic hypoxia and of chickens born from fertilized eggs incubated under hypoxia but kept in the open air after hatching. By comparing the fine structure of the intratectal vessels of chick embryos exposed to hypoxia to that of embryos developed under normal conditions, the conclusion has been drawn that O₂ deprivation does not prevent the temporal sequence of appearance and/or differentiation of the various vascular wall components (endothelium, endothelial basement lamina, pericytes, perivascular glia), but it produces, at least in a part of the latter, modifications, the type and degree of which apparently depend upon hypoxia duration.     

Outgrowth and directional specificity of fibers from embryonic retinal transplants in the chick optic tectum

Retinal pieces taken from known positions of 6-day chick embryos were vitally labeled with the fluorescent dye Rhodamine-B-isothiocyanate (RITC). They were then transferred onto the surfaces of optic tecta following early bilateral removal of the embryo's optic vesicles. One to 5 days after transplantation the tecta were fixed and transplants that issued fibers were examined on tectal whole-mounts or were sectioned and viewed with a fluorescence microscope. Retinal fibers growing out from transplants on day E6 tecta showed a capacity for changing their initial outgrowth directions and for reorienting themselves towards their specific retinotopic projection area. Frequently, changes in growth direction appeared in a right-angled pattern. The capacity for turning was strongest for fibers of nasal retinal origin, less strong for fibers of temporal origin, and occurred rarely but unquantifiably in the case of fibers of ventral retinal origin. Fibers of all investigated retinal quadrants were found to reach their corresponding projection areas and to arborize there, that is, fibers of nasal retinal transplants in the posterior tectum, of temporal transplants in the anterior tectum, and of ventral transplants in the dorsal tectum. Furthermore, once in their target region, the fibers left the outer layer of the tectum and turned, again in right angles, to invade deeper layers. Capacity of fibers to turn towards their projection area was not observed for fibers issued from transplants placed on the tectum later than day E8. We suggest that there is a specific guidance of retinal axons on the tectum.     

Retinal removal up-regulates cannabinoid CB(1) receptors in the chick optic tectum

The endocannabinoid system has been implicated in several neurobiological processes, including neurodegeneration and neuroprotection. The aim of this study was to evaluate the effects of unilateral retinal ablation on the expression of the cannabinoid receptor subtype 1 (CB(1)) at both protein and mRNA levels in the optic tectum of the adult chick brain. After different survival times postlesion (2-30 days), the chick brains were subjected to immunohistochemical, immunoblotting, and real-time PCR procedures to evaluate CB(1) expression. TUNEL and Fluoro-Jade B were used to verify the possible occurrence of cell death, and immunostaining for the microtubule-associated protein MAP-2 was performed to verify possible dendritic remodeling after lesions. No cell death could be observed in the deafferented tectum, at least up to 30 days postlesion, although Fluoro-Jade B could reveal degenerating axons and terminals. Retinal ablation seems to generate an increase of CB(1) protein in the optic tectum and other retinorecipient visual areas, which paralleled an increase in MAP-2 staining. On the other hand, CB(1) mRNA levels were not changed after retinal ablation. Our results reveal that CB(1) expression in visual structures of the adult chick brain may be negatively regulated by the retinal innervation. The increase of CB(1) receptor expression observed after retinal removal indicates that these receptors are not presynaptic in retinal axons projecting to the tectum and suggests a role of the cannabinoid system in plasticity processes ensuing after lesions.     

Microscopical and ultrastructural investigations on the development of the blood-brain barrier in the chick embryo optic tectum

Summary The formation of a blood-brain barrier to horseradish peroxidase was microscopically and ultrastructurally investigated in the tectum opticum of the chick during development of the intraneural blood vessel network from the 6th incubation day to hatching, and in adult specimens.Extravasation of the circulating marker, apparently unimpeded during early stages of vasculogenesis, starts to diminish from the 14th incubation day (i.d.) and is prevented after the 18th i.d. The tracer seems to get out of the vessel lumina through the sites of reciprocal contact between adjacent endothelial cells, and the differentiation of tight junctions there hinders the passage of peroxidase particles. The formation of numerous endothelial vacuoles during early vasculogenesis and the setting of the blood-brain barrier are discussed in connection with the mechanisms of transendothelial transport, and respectively, the processes of moulding of the growing endothelia.     

Topographic projections of the retina and optic tectum upon the ventral lateral geniculate nucleus in the chick

The topographic projections of the retina upon the optic tectum and ventral lateral geniculate nucleus (GLv) of the chick were investigated by making small intraretinal injections of ³H-proline. The retinotectal projection pattern was similar to that described for the pigeon. The retinal projection to the GLv was also topographic and was restricted to the outermost lamina of the nucleus. The anteroposterior retinal axis was reversed in the GLv relative to its orientation in the tectum but the superoinferior axis was oriented identically in both. Furthermore, the posterior retina had an enlarged area of projection in the GLv similar to the enlarged area of retinotectal projection for the “red field” found in pigeons. The tectogeniculate projection was topographic and was confined to the outermost geniculate lamina. The secondorder retionotopic map made by the tectogeniculate projections was in register with the retinogeniculate projection. Although the retinal and tectal projection areas were coextensive in the outermost geniculate lamina, the grain density distributions peaked at different points along a radial path through the geniculate laminae. Injections of HRP into the optic tectum led to very light retrograde labeling of a small population of GLv cells topographically corresponding to the tectogeniculate projection zone of the injection site. The data suggest that the chick GLv is comparable to the GLv of other non-primate mammals.     

Spatial arrangement of radial glia and ingrowing retinal axons in the chick optic tectum during development

Neuroanatomical tracing of retinal axons and axonal terminals with the fluorescent dye, DiI, was combined with immunohistochemical characterization of radial glial cells in the developing chick retinotectal system. Emphasis was placed on the mode of the tectal innervation by individual retinal axons and on the distribution and fate of the tectal radial glial cells and their spatial relation to retinal axons. It was obvious from fluorescent images obtained from anterogradely filled axons that these axons deserted the superficial stratum opticum (SO) to penetrate the stratum griseum et fibrosum superficiale (SGFS) by making right-angled turns within the SO. Frequently, axons which had invaded the SGFS were bifurcated and had a superficial branch which remained within the SO. Terminal axonal arborization occurred at various depths within the SGFS. Characterization of the tectal glial cells and their radial fibers by means of the anti-filament antibody, R5, and post-mortem staining with the fluorescent dye, DiI, revealed the following. (a) At least from day E8 to P1, tectal glial fibers traversed all tectal layers from the periventricular location of their somata to the superficial interface between SO and pia mater. In this interface they enlarged and formed characteristic endfeet. (b) Glial endfeet covered the whole tectal surface. They showed at early ages anterior-posterior differences having a higher density in the posterior tectum. These differences disappeared at embryonic day E13. (c) After innervation, glial endfeet of the anterior tectal third were arranged in rows parallel to the retinal fibers within the SO. This arrangement was not observed in eyeless embryos. (d) Radial glial fibers could be stained with R5 from day E8 to late embryonic stages throughout their entire length. (e) At the first posthatching days, only the segments of the radial glial fibers restricted to the thickness of the SO were R5-positive, although the fibers still traversed throughout the depth of the tectum. The results are discussed in context to the genesis of the retinotectal projection.     

Spatiotemporal gradient of oligodendrocyte differentiation in chick optic tectum requires brain integrity and cell-cell interactions

The development of oligodendrocytes in the chicken optic tectum (OT) was studied in vivo and in vitro by analyzing expression of myelin-associated glycoprotein (MAG) with a monoclonal antibody. MAG(+) cells first appeared in the anterior OT on embryonic day (E) 12, were present throughout the anterior half on E15, and eventually filled the tectum on E17. This spatiotemporal appearance of MAG(+) oligodendrocytes resembled two streams of cells entering the OT along the afferent and efferent axonal layers. However, experiments determined that this appearance of MAG immunoreactivity was the result of a gradient of oligodendrocyte differentiation and was not cell migration. First, retroviral vector labeling of OT progenitors in vivo on E3 resulted in labeled oligodendrocytes in late embryos. In addition, pieces of OT from as early as E3 kept in culture for a week developed numerous MAG(+) oligodendrocytes. Pieces of both anterior and posterior E7 OT developed MAG(+) oligodendrocytes after 3 days in culture, well ahead of their normal schedule in vivo. BrdU incorporation studies revealed that these cells were not born in culture, but merely differentiated. Monolayer cultures made from dissociated E10 or later OT cells developed MAG(+) oligodendrocytes, but monolayers made from E7 OT cells did not. These experiments demonstrate that oligodendrocyte progenitors were present in the OT as early as E3, that they could differentiate precociously, and that their normal progressive differentiation in situ must be due to removal of inhibitory constraints rather than the onset of inductive factors. Also, certain cell-cell interactions occur between E7 and E10, which cannot be disrupted if oligodendrocyte differentiation is to occur.     

Compartmentalization of anterogradely and retrogradely transported organelles in axons and growth cones from chick optic tectum

Previous work suggests that organelles contacting microtubules in axons are in fast transport. Here, we examine the distribution of organelles contacting microtubules in growing axons and growth cones from chick optic tectum. Five axon segments, each 10 microns long, and 4 entire growth cones were reconstructed from serial electron micrographs of quick-frozen, freeze-substituted chick optic tectum. Organelles contacting microtubules in axons are evenly distributed along all microtubules. Smaller organelles, presumably in anterograde transport, are enclosed in fascicles of microtubules, while larger organelles in retrograde transport lie outside the fascicles. In contrast, organelles contacting microtubules are prevalent only in the most proximal parts of the growth cone, before the microtubule fascicles splay out more distally. The distance between noncontacting organelles and microtubules also becomes progressively greater, reaching a maximum in the mid- and more distal region of the growth cone. Contacts with microtubules of both the smaller, presumably anterogradely transported organelles, as well as the larger, presumably retrogradely transported organelles, abruptly become less frequent in the proximal midregion of the growth cone. It is therefore of possible significance in stopping and starting microtubule-based organelle transport that microtubules change from a straight to an undulating configuration in the midregion of the growth cone. The decrease in organelle binding to microtubules at the demarcations between the straight and undulating microtubule segments may depend on proteins or other local factors as well as the splaying out of the microtubule bundles.     

Expression of the AMPA-type glutamate receptor subunits in the chick optic tectum changes biphasically after retinal deafferentation

Effects of retinal lesions on the expression of AMPA-type glutamate receptor (GluR) subunits in the chick optic tectum were evaluated with immunohistochemistry and immunoblotting. Expression of GluR1 and GluR2/3 subunits decreased in the deafferented tectum after 2 days and increased after 7 days postlesion. These results suggest biphasic effects of retinal lesions upon the expression of GluR subunits, possibly due to removal of the glutamatergic input from the retina.