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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 145 (1973), S. 389-416 
    ISSN: 1432-0878
    Keywords: Adrenal chromaffin cells ; Ganglion cells ; Avian adrenal gland ; Light- and electron microscopy ; Histochemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The fine structure of the adrenal gland of 15 bird species was investigated by light-, fluorescence-, and electron microscopy as well as by histochemical methods. 1. Adrenal Chromaffin Cells. Cells producing adrenaline (A) and noradrenaline (NA) may be distinguished from each other with the electron microscope by the different structure of their granules. In all species investigated A-cells prevailed. Granules in A-cells of Corvidae, partly those of the other passeriform birds as well, resemble granules from the pituitary pars intermedia because of their incomplete membrane and the low electron density of their contents. A-cells of some passeriform birds have mitochondria with specifically arranged cristae. Large cytosomes and inclusions of lipofuscin pigment are to be found in the gulls Larus ridibundus and Larus argentatus. The House Sparrow (Passer domesticus) and the Chaffinch (Fringilla coelebs) show vacuoles filled with a colloid-like substance, which are surrounded by adrenal chromaffin cells. 2. Ganglion Cells. The adrenal gland of birds is rich in ganglion cells. Two types can be distinguished. “Large” ganglion cells resemble completely sympathetic nerve cells as described in many vertebrates. “Small” ganglion cells have a low nucleus-cytoplasm-ratio. Some of them include granules of various structure and quantity. Whether they represent transitional stages to adrenal cells, interneurons, P-neurons or a heterogeneous population remains to be clarified.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 146 (1973), S. 385-402 
    ISSN: 1432-0878
    Keywords: Interrenal cells ; Avian adrenal gland ; Lipid exocytosis ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Cords of interrenal-cells of birds resemble “tubes without lumina”, which are lined by columnar cells arranged in double rows. A subcapsular and an inner zone of the interrenal gland may be distinguished according to the structure of their mitochondria, the existence of smooth and rough surfaced endoplasmic reticulum, and the lipid contents. The cells of the inner zone are clearly polarized. The extrusion of lipid by exocytosis is discussed. It is often difficult to decide, whether ultrastructural details are species - specific or indicate a certain state of function.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 145 (1973), S. 557-575 
    ISSN: 1432-0878
    Keywords: Avian adrenal gland ; Adrenergic nerve fibers ; p-Type nerve fibers ; 6-Hydroxydopamine ; Fluorescence microscopy ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Apart from cholinergic nerve fibers, which make up the main part of efferent fibers to the avian adrenal gland (Unsicker, 1973b), adrenergic, purinergic and afferent nerve fibers occur. Adrenergic nerve fibers are much more rare than cholinergic fibers. With the Falck-Hillarp fluorescence method they can be demonstrated in the capsule of the gland, in the pericapsular tissue and near blood vessels. By their green fluorescent varicosities they may be distinguished characteristically from undulating yellow fluorescent ramifications of small nerve cells which are found in the ganglia of the adrenal gland and below the capsule. The varicosities of adrenergic axons exhibit small (450 to 700 Å in diameter) and large (900 to 1300 Å in diameter) granular vesicles with a dense core which is usually situated excentrically. After the application of 6-hydroxydopamine degenerative changes appear in the varicosities. Adrenergic axons are not confined to blood vessels but can be found as well in close proximity of chromaffin cells. Probably adrenergic fibers are the axons of large ganglion cells which are situated mainly within the ganglia of the adrenal gland and in the periphery of the organ and whose dendritic endings show small granular vesicles after treatment with 6-OHDA. A third type of nerve fiber is characterized by varicosities containing dense-cored vesicles with a thin light halo, the mean diameter (1250 Å) of which exceeds that of the morphologically similar granular vesicles in cholinergic synapses. Those fibers resemble neurosecretory and purinergic axons and are therefore called p-type fibers. They cannot be stained with chromalum-hematoxyline-phloxine. Axon dilations showing aggregates of mitochondria, myelin bodies and dense-cored vesicles of different shape and diameter are considered to be afferent nerve endings. Blood vessels in the capsule of the gland are innervated by both cholinergic and adrenergic fibers.
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  • 4
    ISSN: 1432-0878
    Keywords: Thymus ; Myosin ; Actin ; Immunofluorescence microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary A sensitive immunofluorescence microscopical technique employing specific antibodies against highly purified actin and (smooth muscle type) myosin from chicken gizzard and myosin from human striated muscle was used to localize these contractile proteins in the thymus of rat, guinea-pig, cat and chicken. Myoid cells were seen to react with antibodies to striated, but not to smooth muscle type myosin, whereas reticular epithelial cells contained smooth, but not striated type myosin. Actin immunoreactivity was found in both myoid and reticular epithelial cells.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 188 (1978), S. 341-344 
    ISSN: 1432-0878
    Keywords: Peripheral nerves ; Myosin ; Immunofluorescence microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary An indirect immunofluorescence microscopic technique using antibodies from rabbits against highly purified myosin from chicken gizzard was applied to various peripheral nerves (cranial nerves V, VII, X). Myosinspecific immunoreactivity was found in the axoplasm, in Schwann cells, in the perineural sheath and in vascular walls.
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  • 6
    ISSN: 1432-0878
    Keywords: Glial cells ; Myosin ; GFA protein ; Central nervous tissue (rat, human) ; Immunofluorescence microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The glial fibrillary acidic (GFA) protein and myosin were localized in rat spinal cord and human frontal cortex using specific antibodies against GFA protein from human spinal cord and highly purified smooth myosin from chicken gizzard by means of an indirect immunofluorescence microscopical approach. A strong GFA protein and myosin immunoreactivity was found in astrocytes of the white and grey matter and in the external glial limitans membrane. The very fine branches of astrocytic processes stained with antiGFA protein, but not with anti-myosin. Similar results were obtained with the human frontal cortex, where myosin antibodies failed to reveal the very fine branches of protoplasmic astrocytes. As a whole, staining with the GFA protein antiserum was more crisp than with the myosin antibody.
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  • 7
    ISSN: 1432-0878
    Keywords: Actin ; Myosin ; Astrocytes ; Ependymal cells ; Rat diencephalon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Actin and myosin were located in astrocytes, marginal glial and ependymal cells in rat diencephalon by using antibodies against highly purified chicken gizzard actin and myosin. On the basis of these findings it is suggested that glial cell motility in vivo and in vitro is due to the presence of an intracellular actin/myosin system.
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  • 8
    ISSN: 1432-0878
    Keywords: Myosin ; Actin ; Pancreas ; Salivary glands ; Myoepithelial cells ; Immunofluorescence microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Actin and myosin were localized in various salivary glands (parotid, submandibular, sublingual, lingual and Harderian gland) and the exocrine pancreas of rats by indirect immunofluorescence microscopy using specific rabbit antibodies against chicken gizzard myosin and actin. A bright immunofluorescent staining with both antibodies was observed at three main sites: (1) In myoepithelial cells of all salivary glands, (2) in secretory gland cells underneath the cell membrane bordering the acinar lumen (except Harderian and mucous lingual gland), and (3) in epithelial cells of the various secretory ducts (of all glands) in similar distribution as in acinar cells. The present immunohistochemical findings in acinar cells could lend further support to a concept suggesting that myosin and actin are involved in the process of transport and exocytosis of secretory granules.
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