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B E Reese

Publications and source records attributed to B E Reese.

At least 55 records · Page 3Linked to original sources
PubMed1988

Segregation of functionally distinct axons in the monkey's optic tract.

The classical neuro-ophthalmologic literature describes the organization of the primate's optic tract as containing a single topographic representation of the complete contralateral visual hemifield. In contrast, cats have separate visual field representations for the optic axons of the functionally distinct retinal ganglion cell classes. As the line of decussation for each ganglion cell class in the cat occupies a different location on the retinal surface, whereas in primates they are all superimposed, such a species difference might be expected. We report that implants of horseradish peroxidase placed in either the deep or superficial extremes of the monkey's optic tract produce retrograde labelling of distinct retinal ganglion cell classes, and produce anterograde labelling confined to distinct laminae of the lateral geniculate nucleus. Hence, the optic tract of the primate cannot contain a single representation of the contralateral visual hemifield; rather, independent visual field representations for the functionally distinct optic axons must exist. Their anatomical segregation may account for the clinical observation of selective impairments of distinct visual abilities following partial interruption of the optic tract in man.

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PubMed1988

Axon diameter distributions across the monkey's optic nerve.

The distribution of axons according to diameter has been examined in the optic nerve of old world monkeys. Axon diameters were measured from electron micrographs, and histograms were constructed at regular intervals across a section through the optic nerve to reveal the local axon diameter distribution. The total axon diameter distribution was also estimated. Fine-calibre optic axons (less than 2.0 micron in diameter) are found at all locations across the optic nerve. They are most frequent centrotemporally, where very few coarse optic axons can be found, but also make up the majority at the optic nerve's periphery. Coarse optic axons (greater than 2.0 microns in diameter) are increasingly common at progressively peripheral positions in the nerve. Around the nerve's circumference, these coarse optic axons are least numerous temporally, and most common dorsonasally. The axon diameter distribution peaks around 1.25 microns at most locations across the optic nerve, but there are more, slightly larger (1.5-2.0 microns), optic axons dorsally than ventrally. The estimated total axon diameter distribution is unimodal, peaking at 1.0-1.25 microns, with an extended tail towards larger diameters. This centroperipheral gradient of increasing axon diameters across the optic nerve is not substantial enough to account for the partial segregation of axons by size in the monkey's optic tract: there, coarse optic axons form a conspicuously greater proportion of the local axon diameter distribution along the tract's superficial (sub-pial) border, and fine optic axons are the only axons present near the tract's deep border. Hence, the fibre distribution in the optic tract cannot be formed by a simple combination of the fibre distributions of the two respective half-nerves, as described in the classic neuro-ophthalmologic literature. Rather, the present results, in conjunction with previous results from the optic tract, demonstrate that there must be a reorganization of axons by size in or near the optic chiasm.

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PubMed1987

Distribution of axons according to diameter in the monkey's optic tract.

The distribution of axonal diameters in the optic tract of Old World monkeys was examined by light and electron microscopy. Axon diameters were measured in samples of 100 axons taken from several locations in a cross section of the tract about 5 mm behind the optic chiasm. Fine-caliber axons (less than 1.75 micron in diameter) were found in all parts of the tract. Dorsally no coarse axons were present. Further ventrally, coarse axons gradually appeared and increased steadily in proportion. The largest optic axons (greater than 2.5 micron) were found in the most ventral parts of the tract, near the pial surface. This pattern of segregation of axons of differing diameters in the optic tract is a rearrangement of the distribution of axon diameters seen in the nerve rather than a continuation of the same pattern. Examination of axon diameters in the optic nerve has shown that there is a preponderance of fine axons centrally, while coarser axons are found in the periphery, near the pial surface; however, histograms from central parts of the nerve contain a greater proportion of coarse axons than the dorsal parts of the optic tract, while histograms from the periphery of the optic nerve contain a conspicuously greater proportion of fine axons than do histograms from the most ventral parts of the tract. This relatively greater segregation of axons according to diameter in the optic tract demonstrates that the distribution of axons in the tract cannot be formed by the simple combination of two hemiretinal maps contained in each optic nerve, as suggested in classic descriptions.(ABSTRACT TRUNCATED AT 250 WORDS)

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PubMed1987

The crossed projection from the temporal retina to the dorsal lateral geniculate nucleus in the rat.

The crossed projection from the temporal crescent in the rat's retina was studied by producing a discrete retinal lesion in one eye and examining the dorsal lateral geniculate nucleus and superior colliculus contralateral to the lesion for anterograde degeneration products. The position of this crossed degeneration was described in relation to the uncrossed retinal termination in the same structures by injecting the opposite eye with [3H]proline and processing the tissue for autoradiography. The location of the retinal lesion in relation to the temporal crescent was identified by injecting the dorsal lateral geniculate nucleus ipsilateral to the lesioned eye with a fluorescent tracer, to retrogradely label the ipsilaterally projecting retinal ganglion cells in the lesioned eye. Retinal lesions that were histologically verified to be restricted to the temporal crescent produced crossed degeneration in the superior colliculus at its rostral border, in accord with this projection's published visual topography. These same lesions consistently yielded a very circumscribed and sparse amount of degeneration in the contralateral dorsal lateral geniculate nucleus at its dorsomedial border, abutting the optic tract dorsally and the lateroposterior nucleus medially. The degeneration bore no consistent relationship to the position of the uncrossed retinal terminal field, which is situated further ventrally in the dorsal lateral geniculate nucleus; rather, this crossed temporal projection terminated in the outer shell of the nucleus along its medial border. This crossed temporal retinogeniculate projection, together with the crossed projection from nasal retina, forms a continuous map of the complete contralateral retina in the outer shell of the dorsal lateral geniculate nucleus, likely to arise from a population of retinal ganglion cells possessing small soma sizes.(ABSTRACT TRUNCATED AT 250 WORDS)

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PubMed1987

The distribution of axons according to diameter in the optic nerve and optic tract of the rat.

The distribution of axons according to diameter was examined in the optic nerve and optic tract of adult hooded rats. Observations were made on semithin sections, and measurements of axonal diameters were made on electron micrographs taken from various locations across thin sections through the optic nerve and tract. The distribution of axons by size differs markedly in the optic nerve and tract. Coarse (greater than 2 microns) and fine (less than or equal to 2 microns) axons are distributed throughout all regions of the optic nerve. In the optic tract, in contrast, coarse axons are especially dense dorsally, at the deep border of the tract, while they are absent ventrally, subjacent to the pial surface. No regions of the optic nerve contain densities of coarse axons as high as the deep nor as low as the superficial extremes of the optic tract. Nevertheless, even at the deep (dorsal) border of the optic tract, the coarse axons make up only a small minority (roughly 15%) of the total number of axons in that region. The axons 2 microns or smaller may be divisible into two overlapping, fine and intermediate, diameter classes, that are partially segregated within the optic tract, but not in the optic nerve: the distributions of axon diameters smaller than 2 microns are skewed to distinctly smaller diameters at the dorsal and ventral extremes of the optic tract, while in between, at mid-positions along the deep-to-superficial axis of the optic tract, the axon size distributions contain many more axons greater than 1 micron in diameter. These different axon diameter groups may arise from the morphologically distinct retinal ganglion cell types, and may underlie the components of the trimodal compound axon potential seen in the rat's primary optic pathway. Their partial segregation within the tract anticipates the partial segregation of their terminal arborizations within the laminae of the dorsal lateral geniculate nucleus. The rearrangement of axons into a partial segregation by size within the optic tract may indicate a chronology of axonal arrival during early development, proximity to the pial surface being an index of recency of arrival. As axonal outgrowth and neurogenesis appear to be directly related within the retinal ganglion cell population in mammals, the relative birthdates of the retinal ganglion cell types giving rise to the axon diameter classes in the rat may be inferred from the present results.

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PubMed1987

The position of the crossed and uncrossed optic axons, and the non-optic axons, in the optic tract of the rat.

The position of the crossed and uncrossed optic axons, and of the non-optic axons, within the optic tract was determined in the adult hooded rat. Horseradish peroxidase histochemistry and lesion-induced degeneration of axonal profiles were independently used to study the position of the three relevant populations of axons within the optic tract. The boundaries of the optic tract are distinct at all but its caudomedial border, where it abuts the supra-optic commissures running parallel to the fibres of the optic tract. Labelling the crossed population of optic axons, or inducing their degeneration, both demonstrate a clear caudomedial border of the optic tract, although a number of optic axons stray out of the optic tract and course within the supra-optic commissures immediately caudomedial to the tract. The uncrossed optic axons are, as a population, positioned relatively deep in the optic tract, towards its dorsal border. A few occur at further ventral positions, but their density is greatly reduced there. There is also a very thin region along the dorsalmost edge of the optic tract free of uncrossed optic axons. The relative position of the uncrossed to the crossed optic axons is discussed in the context of the mammalian optic tract as a chronological map: spatial position in the tract may reflect temporal order of axonal arrival during early development. A large population of non-optic axons belonging to Gudden's commissure courses within the boundaries of the optic tract at a relatively ventral position. They are most frequent caudomedially, and are absent rostrolaterally. Hence, axons of the optic tract and Gudden's commissure are substantially intermingled in the caudomedial half of the optic tract. These non-optic axons greatly outnumber the uncrossed optic axons, and will consequently distort counts of uncrossed optic axons based on intact profiles that remain after removal of the opposite eye. However, they are still a minority in comparison to the crossed optic axons in this region.

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PubMed1986

The topography of expanded uncrossed retinal projections following neonatal enucleation of one eye: differing effects in dorsal lateral geniculate nucleus and superior colliculus.

The topographic organization of the uncrossed retinal projections to the dorsal lateral geniculate nucleus (dLGN) and superior colliculus (SC) was studied in normal adult hooded rats and in rats subjected to unilateral ocular enucleation on the day of birth. Sections were stained for anterograde degeneration products following discrete retinal lesions at various locations. The projection from the temporal crescent to the dLGN in neonatally enucleated rats had an expanded but topographically normal organization, with the nasotemporal and dorsoventral retinal axes displaying polarities identical to those in normal adults. Neonatal enucleation permits the remaining uncrossed retinogeniculate projection to extend primarily along the "lines of projection" into neuropil normally recipient of binocularly conjugate crossed projections. In the SC, the dorsoventral axis of the temporal crescent showed a normal polarity, but the nasotemporal axis failed to display any topographic organization. Retinal loci in the temporal crescent projected throughout the rostrocaudal extent of the ipsilateral SC. Retinal lesions placed outside the temporal crescent failed to produce any substantial degeneration in ipsilateral dLGN or SC. These topographically distinct effects in dLGN and SC following unilateral eye removal on the day of birth are discussed in the context of differing constraints upon axonal ingrowth and connectivity during early development, which may normally bring about the characteristically distinct features of retinogeniculate and retinocollicular organization.

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PubMed1986

Large retinal ganglion cells in the rat: their distribution and laterality of projection.

The distributions of the ipsilaterally and contralaterally projecting large ganglion cells in the retina of the rat were determined, using the retrograde transport of Horseradish peroxidase (HRP) following injections into one optic tract. Labelled large retinal ganglion cells occur throughout the contralateral retina and throughout the temporal crescent of the ipsilateral retina, but there is a noticeable decrease in their density in the contralateral retina's temporal crescent. This retinal region was identified in these same retinae by injecting a retrogradely transported fluorescent tracer into the optic tract opposite that receiving the HRP. The density of large retinal ganglion cells increases in both the contralateral retina and the ipsilateral temporal crescent in the upper temporal periphery such that, together, these two populations of large cells combine to produce a peak density centred on the retinal representation of the visual field's vertical midline. This peak density of large retinal ganglion cells must therefore be further peripheral than the peak density for the total population of retinal ganglion cells, since all evidence indicates that the latter is positioned nasal to the vertical midline's representation. This was verified in one rat, in which the density distribution of the total population of retinal ganglion cells was determined and compared with the distribution of the large cell population. The results suggest that the rat possesses a specialized retinal focus of large ganglion cells for viewing the visual field directly in front of the animal.

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PubMed1985

Rearrangements in the retino-geniculate projections of rats following ablation of the superior colliculus in infancy.

The superior colliculus was bilaterally or unilaterally ablated at different early postnatal ages in rats. When adult, each rat received a unilateral eye injection of Horseradish peroxidase to reveal the crossed and uncrossed retinal terminal fields within the dorsal lateral geniculate nucleus. Collicular ablation in the first seven days after birth, but not thereafter, produced a small hole or vacancy within the contralateral retinal terminal field which was occupied by an aberrant ipsilateral retinal terminal field. These rearrangements in the retino-geniculate projections occurred in the caudal quarter of the nucleus dorso-laterally just beneath the optic tract, solely ipsilateral to the ablated colliculus. Possible causes of the formation of these rearrangements are discussed, and similarities with other aberrant retinal projections following early damage to the visual system are considered.

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PubMed1985

The topography of aberrant ipsilateral retinogeniculate projections following neonatal ablation of the superior colliculus in rats.

The topography of aberrant ipsilateral retinogeniculate projections following ablation of the superior colliculus in infancy has been examined. Rat pups received a unilateral ablation of the superior colliculus in infancy, which is known to produce an aberrant ipsilateral retinogeniculate projection in the caudal quarter of this nucleus, ipsilateral to the ablation. When adult, each rat received a retinal lesion in the eye ipsilateral to the ablation at varying locations along the temporal crescent and the brains were subsequently processed for anterograde degeneration. The topographic relationship between the retina's temporal crescent and the ipsilateral dorsal lateral geniculate nucleus appeared normal in the rostral three quarters of the nucleus, but an aberrant projection from the far temporal retina (the upper temporal crescent) was demonstrated in the caudal quarter of the nucleus, residing dorsolaterally beneath the optic tract. This location within the dorsal lateral geniculate nucleus normally receives its retinal input from the contralateral temporal retina at reduced eccentricity. As these two retinal regions are likely to be binocularly conjugate, it is proposed that these rearrangements in retinal terminal fields following early collicular ablation produce an ocularly aberrant yet visuotopically appropriate retinogeniculate projection.

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PubMed1983

Projection lines and the ipsilateral retino-geniculate pathway in the hooded rat.

The organization of the hooded rat's dorsal lateral geniculate nucleus was studied with anatomical techniques, with particular regard to the representation of temporal retina and the binocular field. The ipsilateral and contralateral retinal terminal fields were examined in three stereotaxic planes following injections of horseradish peroxidase into the eye. Projections arising from the temporal crescent of the retina were studied with silver staining techniques for anterograde degeneration products. Following discrete retinal lesions there was clear evidence that the temporal retina projects in a topographic fashion both ipsilaterally and contralaterally. The orientation of the lines of projection in the dorsal lateral geniculate nucleus was assessed by retrograde labelling of cells after cortical implants of horseradish peroxidase. Although both the lines of projection and the ipsilateral terminal field extend rostro-caudally in the dorsal lateral geniculate nucleus, their paths are oblique rather than parallel. Their intersection appears to correspond to the representation in this nucleus of conjugate retinal points. This was confirmed by administering horseradish peroxidase by iontophoresis in either the binocular or monocular representation of the primary visual cortex, while one eye received an injection of [3H]proline. Only those cortical injections in the binocular region gave rise to labelled projection lines passing through the autoradiographically-labelled ipsilateral terminal field. The rat's dorsal lateral geniculate nucleus displays none of the cytoarchitectural lamination which is so prominent in the primate and cat. Even after labelling the input to the nucleus from one eye, there is still no obvious laminar relationship between the terminal fields from the two eyes. Despite the absence of lamination, the current results suggest that the principle of apposing the representation of conjugate retinal points in the dorsal lateral geniculate nucleus is the same in the rat as in cat and monkey.

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PubMed1983

Crossed and uncrossed visual topography in dorsal lateral geniculate nucleus of the pigmented rat.

1. The representation of the retinocentric visual field within the dorsal lateral geniculate nucleus (dLGN) was assessed electrophysiologically by recording multicellular responses from anesthetized pigmented rats. Separate experiments examined the representation through either the contralateral or ipsilateral eye along the dorsoventral, mediolateral, and rostrocaudal dimensions of the nucleus. 2. The crossed projection displays an orderly representation of the visual field, mapping eccentricities out to 100 degrees from the optic disk. There is, however, a marked absence of eccentricities greater than 60 degrees representing upper nasal visual space. The uncrossed projection also displays an orderly representation of the visual field but is limited in extent to upper nasal visual space at far eccentricities of 50-90 degrees. 3. The ipsilateral projection, which represents far eccentric upper nasal visual space, occupies a region in the contralateral representation corresponding with upper nasal visual space at reduced eccentricity. It is these two regions that are considered binocularly conjugate: the temporal crescent of each eye with another crescent (the conjugate central crescent) lying between the optic disk and the temporal crescent of the opposite eye. It is suggested that the crossed and uncrossed representations are aligned in the dLGN so that projection lines for discrete regions of the binocular visual field course through the nucleus from rostroventral to caudodorsal. Although the dLGN of the rat lacks the cytoarchitecturally distinct laminae associated with the regions of afferent input from each eye, as is seen in the primate and cat dLGN, the organizing principle of apposing the representation of the visual field through each eye is similar.

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PubMed1982

Restricting eye movements in the anesthetized rat: a comparison of four techniques.

Four techniques for the immobilization of rodent eyes were compared. Eye movements were plotted over a three hour period by reflecting a laser beam off a small mirror affixed to the cornea. Surgical techniques for producing local paralysis of the extra-ocular eye muscles were inconsistently successful. Physical stabilization techniques reliably reduced eye movements to an extent compatible with certain neurophysiological tests. None of the techniques was as efficacious as the use of neuromuscular blocking agents combined with physical restraint.

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PubMedDate not supplied

'Hidden lamination' in the dorsal lateral geniculate nucleus: the functional organization of this thalamic region in the rat.

The cyto-and myeloarchitecture of the rat's dorsal lateral geniculate nucleus (dLGN) display none of the laminar features characteristic of this thalamic region in carnivores and primates. Despite this, the rodent's nucleus contains a segregation of functionally and ocularly distinct afferents--organizational properties manifested in the prominent lamination of these other mammalian forms. The rat's dLGN can be divided into two main regions: an inner core and an outer shell. The inner core contains two ocular laminae receiving direct retinotopic projections from the contralateral nasal and ipsilateral temporal retinae, mapping the contralateral visual hemifield. The outer shell receives a retinotopic projection from the complete contralateral retina only, the representation of the ipsilateral hemifield being extremely compressed at the medial edge of this lamina. The retinotopic maps in these three ocular laminae (contra, ipsi, contra) are in conjugate register, so that lines of projection course rostro-ventro-medially from the optic tract at the thalamic surface through these laminae. Three morphologically distinct retinal ganglion cell types project to the dLGN, and the axons of these ganglion cells are partially segregated within the optic tract in anticipation of their segregation within the nucleus, where they terminate at distinct locations along the lines of projection. Type I and III cells terminate in the inner core of the nucleus, while type II and III cells terminate in the outer shell. The outer shell also receives a direct projection from the superior colliculus. These characteristics of the afferent termination within the rat's dLGN support the view of a general mammalian plan for the organization of this thalamic region, and provide a basis for further experimentation to test speculations about potentially homologous subdivisions of this nucleus. Conclusions regarding functionally analogous pathways are proposed with less confidence, due to the paucity of definitive evidence for physiologically distinct cell classes. The type I cells in the rat's retina are the likely homologues of the cat's alpha-cell. Geniculocortical relay cells driven by them have properties similar to the cat's Y-cell. The inner core of the nucleus then may transmit information of a Y-like nature onto striate cortex. The outer shell of the rat's nucleus, a portion of which receives collicular as well as retinal innervation, may convey W-like information onto striate cortex. The rat's retinogeniculate projection appears to be lacking a beta-cell-like pathway that may subserve X-cell function altogether.

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PubMedDate not supplied

Does early enucleation affect the decussation pattern of alpha cells in the ferret?

Naturally occurring cell death has been hypothesized to sculpt various features of the organization of the mature visual pathways, including the recent proposal that the selective elimination of ganglion cells in the temporal retina shapes the formation of decussation patterns. Through a class-specific interocular competition, ganglion cells in the two temporal hemiretinae are selectively lost to produce the decussation patterns characteristic of each individual cell class (Leventhal et al., 1988). The present study has tested this hypothesis by asking whether the removal of one retina in newborn ferrets, which should disrupt binocular interactions at the level of the terminals, alters the decussation pattern of the alpha cells, a cell class that is entirely decussating in the normal adult ferret. Enucleation on the day of birth was found to increase the uncrossed projection by approximately 50%, but not a single uncrossed alpha cell was found in the temporal retina. Either alpha cells never project ipsilaterally during development, or if they do, they cannot be rescued by early enucleation. While naturally occurring cell death plays many roles during development, creating the decussation pattern of the ferret's alpha cell class via a binocular competition at the level of the targets is unlikely to be one of them.

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PubMedDate not supplied

The re-establishment of the representation of the dorso-ventral retinal axis in the chiasmatic region of the ferret.

This study has examined the representation of the dorso-ventral retinal axis in the optic nerve and tract of the ferret, as well as the associated fiber transformations which take place within the chiasmatic region. In one series of experiments, dorsal or ventral retinal lesions were made to induce fiber degeneration along the pathway, from which semi-thin sections were then stained for degenerating myelin. In a second series, implants of the carbocyanine dye, DiI, were made into the caudo-medial or rostro-lateral optic tract in order to label retrogradely the axons as they course through the chiasmatic region. Additional observations were made from the optic pathways of ferrets that had been similarly lesioned or implanted, but employing either a reduced-silver technique to reveal the degenerating axons or horseradish peroxidase as the retrograde label. The axons arising from the dorsal and ventral retina course in the dorsal and ventral parts of the optic nerve posterior to the eye, but as they continue along the nerve they disperse producing a highly impoverished retinotopy in the prechiasmatic portion of the nerve. As they course through the chiasmatic region, however, they become segregated again: dorsal fibers cross the midline relatively caudally while ventral fibers cross further rostrally, although there is overlap between them. Nearer the threshold of the optic tract, the fibers from dorsal and ventral retina undergo a further and more striking segregation, placing the dorsal fibers caudo-medially and the ventral fibers rostro-laterally within the tract. This re-emergence of retinotopic order implicates a fiber-substrate interaction as being responsible for the axonal reordering, and suggests that fiber pre-ordering in the tract contributes to the formation of the orderly projection of the dorso-ventral retinal axis upon central visual targets.

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PubMedDate not supplied

Organization of retinal ganglion cell axons in the optic fiber layer and nerve of fetal ferrets.

Previous authors have hypothesized that retinotopic projections may be influenced by 'preordering' of the axons as they grow towards their targets. In some nonmammalian species, axons are reorganized at or near the optic nerve head to establish a retinotopic order. Data are ambiguous concerning the retinotopy of the mammalian retinal nerve fiber layer and whether fibers become reorganized at the optic nerve head. We have examined this question in fetal and newborn ferrets (Mustela putorius furo) by comparing the arrangement of axons in the retinal nerve fiber layer with that in the optic nerve. Dil or DiA crystals were implanted into fixed tissue in the innermost layers of the retinal periphery, or at a location midway between the periphery and the optic nerve head. Fluorescence labelling was examined in 100-200 microns Vibratome sections, or the eyecup and nerve were photooxidized and 1-2 microns longitudinal or transverse sections were examined. Regardless of fetal age, eccentricity or quadrant of the implant site, a segregation of labelled peripheral axons from unlabelled central ones was not detected within the nerve fiber layer. Axons coursed into the nerve head along the margin of their retinal quadrant of origin, often entering the optic nerve as a radial wedge, thus preserving a rough map of retinal circumference. However, peripheral axons were in no way restricted to the peripheral (nor central) portions of the nerve head or nerve, indicating that the optic axons do not establish a map of retinal eccentricity. Our results demonstrate that (1) the nerve fiber layer is retinotopic only with respect to circumferential position and (2) optic axons are not actively reorganized to establish a retinotopic ordering at the nerve head. The present results suggest that any degree of order present within the optic nerve is a passive consequence of combining the fascicles of the retinal nerve fiber layer; optic axons are not instructed to establish, nor constrained to maintain, a retinotopic order within the optic nerve.

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