Laterality of spinocerebellar neurons in the chicken spinal cord.

The aim in this study is to elucidate the laterality of chicken spinocerebellar (SC) neurons that originate from the caudal cervical to caudal lumbosacral spinal cord. SC neurons in the spinal segment (SS) 17-20 consisted of a mixture of crossed and uncrossed axons. SC neurons in the more cranial and caudal SS than SS 17-20 (transitional zone) were generally uncrossed and crossed, respectively. In the transitional zone, SC neurons in spinal border cells and ventral border cells of the ventral horn changed dramatically from an uncrossed to a crossed type between SS 17 and SS 18. Chicken SC neurons are markedly different in laterality from mammalian SC neurons.

Trajectories in the spinal cord and the mediolateral spread in the cerebellar cortex of spinocerebellar fibers from the unilateral lumbosacral enlargement in the chicken.

Spinocerebellar (SC) neurons in the lumbosacral enlargement (LSE) give rise mainly to crossed fibers and generally terminate in parasagittal bands in the granular layer of the chicken cerebellar cortex. However, parasagittal bands for mossy fiber terminals have not always been clear in some cerebellar folia. The present study aimed at (1) observing the course in the spinal cord of the spinocerebellar tracts (SCTs), (2) confirming whether SC fibers originating from the unilateral LSE terminate in parasagittal bands, and (3) elucidating the relationship between the ventral and lateral funicular parts of the SCTs in the cervical enlargement (CE) using anterograde and retrograde labeling methods. The SCTs were located in the medial part of the ventral funiculi in spinal segment (SS) 27, the full width of the ventral funiculi in SS 22, the lateral and ventral funiculi in SS 14 and in the lateral funiculi from SS 10 rostralward. Projection areas in the cerebellar cortex of SC fibers were studied following unilateral injections of WGA-HRP into the LSE. As a result, SC fibers from the LSE terminated bilaterally in parasagittal bands of folia II-VI and IXc. Labeled terminals in the injected side were similar in number to those in the other side in folia II-IV and IXc and more than those in the other side in folia V and VI. Following ablation of the left (contralateral) lateral funiculus of the CE, the same tracer was injected into the right (ipsilateral) LSE or into the anterior or posterior cerebellar lobe. As a result, anterogradely labeled SC fibers passing through the ventral funiculus in the CE mainly terminated in the contralateral cerebellar cortex in folia II, III and IV, and in the ipsilateral cerebellar cortex in folia V, VI and IX. Following ablation of the unilateral lateral funiculus, retrogradely labeled neurons in the contralateral LSE were found in all SC neuron groups showing marked reduction in number. Thus, the ventral and lateral funicular parts of the SCTs in the CE were not pathways for specific SC neuron groups but different in projection areas.

Constitution of the ependyma in the chicken telencephalon.

The constitution of ependyma derived from the ventricular zone is different from that derived from other regions of the central nervous system. In the mammalian cerebrum, the ependyma is varied by the regions to cortex or basal ganglia (BG). In the avian telencephalon (Tc), previous studies about the constitution of the ependyma have not revealed clear findings. In the present study, we performed immunostaining of ependymal cells in the chicken Tc to confirm differences in the ependyma of various regions. As a result, 4 patterns of ependyma were defined in the outer side of the lateral ventricle. In the base of the lamina pallio-subpallialis (LPS), ependyma consisted of vimentin/glial fibrillary acidic protein (GFAP) double-positive cells, whereas in the base of the lamina frontalis superior, it consisted primarily of vimentin-positive cells and a small number of vimentin/GFAP double-positive cells. With the exception of the above, the pallial ependyma was a single layer containing vimentin single-positive cells. Lastly, the ependyma of the BG was rich in vimentin single-positive cells. The constitutional differences of the ependyma of the pallium and BG concerned differences in ependymal morphology and cell characteristics. These finding suggest that the bounder between pallium and BG is LPS at the point of ependyma.

Spinocerebellar projections from the cervical and lumbosacral enlargements in the chicken spinal cord.

In birds, spinocerebellar (SC) projections to the cerebellar cortex have not been understood well. We examined SC fiber terminal fields originating from the cervical and lumbosacral enlargements (CE and LSE, respectively) in the chicken. SC fiber terminals show parasagittal bands in the granular layer. Labeled terminals from the CE were distributed primarily in folia II-V and IX. Parasagittal bands of labeled terminals from the CE were not clearly separated in folia II and III but were clearly separated in folia IV and V. In folium IX, labeled terminals were diffusely distributed in all subfolia with no evidence of banding. The numbers of bands were 5 in folium II, 12 in folium III and 7 in folia IV and V at maximum. Labeled terminals from the LSE were distributed primarily in folia II-VI and IX. Labeled terminals from the LSE were arranged in 4 bands in folium II and in 8 bands in folium III at maximum. Parasagittal bands from the LSE in folia IV and V were not clearly separated. In folium VI, the numbers of parasagittal bands was 6 at maximum. In folium IX, labeled terminals were mainly found in subfolium IXc forming 6-8 parasagittal bands. There were more parasagittal bands of labeled terminals from the CE than from the LSE. The topography of SC fiber terminals from the CE was different from that of SC fiber terminals from the LSE.

Distribution of astroglial lineage cells in developing chicken telencephalon from embryo to young chick.

The largest area of the avian telencephalon (Tc) is the subpallium [basal ganglia (BG)], and the pallium (cortex) is a narrow area located at the surface of the Tc. However, recent studies have proposed that most of the area of the avian Tc is the pallium, which corresponds to the cerebral cortex of mammals. This theory is based on neuronal elements with little regard to glial cells, which play important roles in neurogenesis. In the present study, we observed the distribution of glial cells using immunohistochemistry during maturation and discuss the division of the Tc by glial elements. In the early stage, the distribution and morphology of vimentin-positive radial glial cells were different between dorsal and ventral areas when they began to spread their processes toward the pia matter. During the development stage, vimentin-positive long processes divide the pallium and BG by the lamina pallio-subpallialis. Moreover, the pallium was divided into four regions by vimentin and glial fibrillary acidic protein-positive elements in the later stage.