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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 229 (1983), S. 299-308 
    ISSN: 1432-0878
    Keywords: Adrenal chromaffin cells ; Plasticity ; Transplants ; Kidney capsule ; Ultrastructure ; Catecholamine biochemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Histochemical, ultrastructural and biochemical studies (quantitative determinations of catecholamines (CA) and phenylethanolamine N-methyltransferase (PNMT) activity) were carried out on autologous transplants of adult guinea-pig adrenal medulla under the kidney capsule, in order to investigate the specific influences of a virtually nerve-free environment in comparison to those mediated by a densely innervated one such as in the iris (cf. Unsicker et al. 1981). Three weeks after transplantation chromaffin cells survived well, most cells maintaining their morphological identity in terms of adrenaline (A) storage, although biochemically measured A and PNMT had dramatically decreased. Chromaffin cells in transplants extended neurite-like processes in an identical fashion as seen in transplants to the anterior chamber of the eye and in culture. Chromaffin cells were frequently connected by synaptoid contacts, but did not receive cholinergic synapses as observed in transplants to the iris. It may be concluded that the growth factor(s) eliciting neurite outgrowth from transplanted chromaffin cells are rather ubiquitously present, independent of whether the transplantation site is sparsely or richly innervated.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 215 (1981), S. 341-367 
    ISSN: 1432-0878
    Keywords: Adrenal chromaffin cells ; Plasticity ; Eye chamber transplants ; Ultrastructure ; Catecholamine biochemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Autografts of adrenal chromaffin cells from adult guinea pigs to the anterior chamber of the eye were studied electron microscopically and both histo-and biochemically 4, 8 and 12 weeks after transplantation. Transplanted chromaffin cells resembled in many respects their in-situcounterparts: they stored varying amounts of granular vesicles, which were reduced in diameter, but displayed mostly cores of low or medium electron densities suggesting predominant storage of a secondary amine. Concomitant biochemical determinations of catecholamines (CA) and phenylethanolamine N-methyltransferase (PNMT) activity revealed a distinct reduction of total CA and PNMT activity, but no change in the proportion of adrenaline (A) to noradrenaline (NA) after 4 weeks. However, an increase of NA and almost equal amounts of A and NA were found after 8 weeks. CA-histofluorescence and electron microscopy revealed that axon-like processes with varicosities extend from chromaffin cells and contain the large “chromaffin” vesicles (100–200 nm in diameter) in addition to small clear and dense-cored vesicles (40–80 nm in diameter). Processes of chromaffin cells grew in all directions over the host iris and were also found in close proximity to smooth muscle cells the sympathetic nerve supply of which had been cut by removing the superior cervical ganglion. Administration of 5-and 6-hydroxydopamine (OHDA) resulted in characteristic labeling and ultramorphological changes in axons, but caused alterations in chromaffin cell bodies only 8 weeks after transplantation. Transplanted chromaffin cells became reinnervated by nerve fibres that are considered to be cholinergic fibres derived from the ciliary ganglion. Transplanted chromaffin cells also exhibited synapse-like contacts with each other. The present study shows that chromaffin cells from adult guinea pigs transplanted to the anterior chamber of the eye retain a large number of differentiated properties. Formation of axon-like processes by these cells indicates that the anterior chamber of the eye favours transdifferentiation, as does tissue culture (Unsicker et al. 1978a), eliciting a cell type that displays features of both a sympathetic neurone and a SIF-cell.
    Type of Medium: Electronic Resource
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