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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 68 (1985), S. 169-172 
    ISSN: 1432-0533
    Keywords: Astroglia ; Oligodendroglia ; Gliogenesis ; Developing spinal cord ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The identity of mitotic cells in the ventral half of the irradiated spinal cord in 13-day-old rats was studied by light and electron microscopy. At this post-irradiation interval, astrocytes as well as oligodendrocytes are markedly reduced in both gray and white matter, and few myelin sheaths are present. Earlier studies showed incorporation of3H-thymidine into cells identified light-microscopically as neuroglia. In the present study, a number of mitotic cells were identified in thick plastic sections. When adjacent thin sections were examined by electron microscopy, these mitotic cells were identified ultrastructurally as astroglia on the basis of the bundles of filaments in their cytoplasm and the irregular outline of the cell body and its processes. It is apparent from this study that astroglia proliferate prior to the delayed myelination that occurs later in the glial cell deprived ventral irradiated cord.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 76 (1988), S. 624-627 
    ISSN: 1432-0533
    Keywords: X-Irradiation ; Intraspinal Schwann cell ; Myelin ; Autoradiography ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A stable population of intraspinal Schwann cells, which developed follwing early postnatal irradiation of the spinal cord, was challenged by the addition of tellurium (Te) to the diet beginning at 30 days of age. Schwann cells incorporating [3H]thymidine were identified by 1 μm autoradiographs and by conventional electron microscopy of adjacent thin sections. Autoradiographs of areas with Schwann cell myclination showed extensive labelling of cells in the Te-fed animals. In contrast, control animals which were not fed Te showed little evidence of labelled Schwann cells. These data indicate that Schwann cells in the intraspinal environment show a proliferative response to the presence of Te in the rat's diet, as do Schwann cells in their normal extraspinal milieu.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 99 (1994), S. 25-33 
    ISSN: 1432-1106
    Keywords: Regeneration ; Schwann cells Glial environment ; X-Irradiation ; Astrocytes ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Exposure of the lumbar spinal cord of rats to X-rays 3 days after birth results in changes in the composition of central glia. Shortly after irradiation, there is both retardation of central myelin formation and a loss of integrity of the astrocyte-derived glia limitans on the dorsal surface of the cord. Subsequently, Schwann cells invade, undergo division and myelinate axons in the dorsal funiculi in the irradiated region of the cord, creating there an environment similar to that of peripheral nerve. The present study was undertaken to compare the ability of lesioned dorsal root axons to grow back into the altered glial environments that exist within the spinal cord after irradiation. This regrowth was assessed by injecting Fluoro-Gold into the spinal cord and subsequently examining neurons in the dorsal root ganglia (DRG) for the presence of this label. Numbers of retrogradely labeled neurons were counted in the DRG in both injured and contralateral non-injured sides. Non-irradiated control rats had almost no labeled DRG neurons on the injured side, whereas Fluoro-Gold labeled neurons were observed in substantial numbers in the DRG on the injured side of irradiated rats. There was a definite trend in the data, indicating that the longer the interval between irradiation and root injury, the greater the number of labeled neurons. Since the Fluoro-Gold labeling technique does not allow for visualization of the labeled axons within the spinal cord, a few animals were used to assess anterograde labeling with wheat germ agglutinin-conjugated horseradish peroxidase (WGA-HRP/HRP) from the dorsal root into the spinal cord. HRP-filled regenerating axons were visualized in dorsal white and gray matter of the irradiated spinal cord. Such axons were not present in the non-irradiated spinal cords. Radiation-induced changes in glial populations are discussed, particularly with regard to the temporal sequence of these changes and their possible relationship to the conversion of a normally non-permissive environment into one conducive to axonal regrowth.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 75 (1989), S. 513-522 
    ISSN: 1432-1106
    Keywords: Spinal cord ; Myelin ; Oligodendrocyte ; Schwann cells ; Tropic signals
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Irradiation of the rat spinal cord during the first postnatal week results in a profound reduction of oligodendrocyte myelin formation in the dorsal funiculi (DF). Despite this absence of myelin, however, axons in the irradiated region in the DF increase in diameter and approximate the size distribution seen in the control spinal cord. By 25 days of age Schwann cells are present in the irradiated DF where they undergo cell division and myelinate the axons. During the early stages of this myelin formation, these intraspinal Schwann cells exhibit a relationship to axons that is somewhat different from that seen in the normal developing peripheral nervous system (PNS). For example, within a given region, intraspinal Schwann cells myelinate axons of large diameter prior to ensheathing bundles of small diameter axons. Additionally, during myelination a Schwann cell will surround a single axon with multiple processes which appear to compete for contact with the axolemma. On axons of larger diameter, the elaboration of these processes is so excessive that it is often difficult to trace them back to the parent Schwann cell. Later, when a single process establishes several spirals about an axon, additional processes are no longer elaborated, and the “extra” processes disappear as myelin formation advances to the stage of compact lamellae. Thereafter, the myelin sheath continues to form in a normal manner. Excess processes have been observed during myelinogenesis in the normal developing PNS, but their frequency in that environment is much less than in the irradiated cord. These observations support the hypothesis that the signal(s) to initiate myelin formation are expressed on the axolemmal surface and are controlled by the neuron. In addition, these observations suggest that the delay in myelination results in an affinity or tropism between axons and Schwann cells which exceeds the level existing at the normal time of myelin formation.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 186 (1976), S. 437-449 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The appearance and development of the primary and secondary sympathetic trunks in staged chick embryos was studied using the Falck-Owman histochemical method for the demonstration of primary monoamines. The earliest appearance of catecholamine (stage 20) was in individual fluorescent cells located in the region of the dorsal root ganglia about two stages prior to the formation of primary trunk aggregates. These cells are believed to be sympathetic precursor cells and correspond to formaldehyde-induced fluorescent cells observed in recent explantation experiments. Aggregates of fluorescent cells had formed bilaterally dorsolateral to the aorta at stage 22. These aggregates became continuous to form primary trunks by stage 24. The secondary sympathetic trunks were first seen in stage 25 and appeared to form at least partially by dorsal migration of cells from the primary trunks. Fluorescent cell processes were first observed at this stage. Secondary trunk formation was essentially complete by stage 28, and the primary trunks had become small and discontinuous. Definite rami communicantes could be observed by the early part of stage 28 in silver preparations. The significance of the development of two successive trunks in avians is discussed.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 161 (1981), S. 311-321 
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The entopeduncular nucleus (EN) in the cat, the homologue of the primate internal globus pallidus and main output of the basal ganglia, is known to project to the mesencephalic tegmentum. We have been able to elicit antidromic responses in single EN neurons from a site in the posterior mesencephalon, then transect the brainstem (precollicular-postmamillary) and elicit locomotion and rhythmic movements of the limbs by stimulation of the same site in the same animal. These studies demostrate the existence of a direct projection from the EN to the mesencephalic locomotor region (MLR). However, this is not a particularly large pathway since fewer than 5% of the EN cells appear to project to the MLR.In a parallel series of anatomical experiments, injections of fluorescent dyes into the area of the MLR induced retrograde labeling of cell bodies in the EN and motor cortex. Injections of tritiated amino acids into the motor cortex resulted in labeling in the area anterior to the MLR. We assume that these connections may be involved, in part, in the sequencing and ordering of series of voluntary movements in which locomotion is involved.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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