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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 261 (1990), S. 539-547 
    ISSN: 1432-0878
    Keywords: Nerve growth factor ; Organ culture ; Seminiferous tubules ; Germ cell degeneration ; Lamina-propria cells ; Sertoli cells ; Human
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Seminiferous tubules from human testes were mechanically isolated, the cut edges were sealed, and the tubules were cultured in medium free of fetal calf serum (FCS). Degeneration of germ cells occurred during the culture period and was paralleled by a disruption of the seminiferous epithelium, a disturbance in morphology and function of Sertoli cells, and a thickening of the lamina propria. However, when tubules were cultured for 5 days in the presence of FCS, degeneration of the spermatogenic tissue was reduced. FCS increased the mitotic activity of germ cells, but did not maintain normal morphology and function of Sertoli cells and cellular elements of the lamina propria. The thickening of the tubular wall concurred with a change in phenotype of lamina-propria cells from myoid to fibroblastic. Addition of nerve growth factor (NGF) to the culture medium (i) maintained the myoid phenotype of lamina-propria cells, (ii) prevented thickening of the tubular wall, and (iii) stabilized Sertoli cell morphology and function. The effects of NGF appeared to depend on the trophic effects of FCS, since NGF alone had no influence on the maintenance of a regular morphology of the spermatogenic epithelium. The present results indicate a decisive role for NGF in stabilizing specific functions of seminiferous tubules.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 261 (1990), S. 549-554 
    ISSN: 1432-0878
    Keywords: Nerve growth factor receptor ; Testis ; Cell culture ; Cell plasticity ; Lamina-propria cells ; Human
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Nerve growth factor (NGF) affects morphology and function of isolated and cultured seminiferous tubules from human testis. Quanitative determination of this neurotrophic protein revealed an amount of 5.4 ng per g human testis, suggesting a crucial function of NGF in spermatogenic tissue. With the use of immunohistochemical methods target cells for NGF were identified within the lamina propria. NGF receptors were also visualized on sympathetic nerve fibers crossing the interstitial compartment among adjacent tubules and spatially correlated blood vessels. NGF receptors could be demonstrated on isolated lamina-propria cells even after 2 weeks of culture. Most of the NGF receptor-bearing cells differed from myoid cells of the lamina propria expressing desmin, a marker for smooth muscle. However, some NGF receptor-expressing cells were found sharing morphological and structural similarities with myoid cells. The present data indicate the existence of a NGF-responsive lamina-propria cell that influences the tubular wall and also the seminiferous epithelium.
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  • 3
    ISSN: 1432-0878
    Keywords: Key words: Urothelium ; Tartrate-resistant acid phosphatase ; Nitric oxide synthase I ; Superoxide dismutase ; Immunocytochemistry ; Free radicals ; Human
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. Three enzymes, viz., tartrate-resistant acid phosphatase (TRAP), nitric oxide synthase I (NOS-I), and superoxide dismutase (SOD), involved in the production and metabolism of free radicals or radical equivalents, were demonstrated by immunocytochemistry in the urothelium of the ureters of six patients of various ages. Two of these enzymes (TRAP and NOS-I) were colocalized in the most apical and lateral border of the superficial cells of the urothelium. In contrast, SOD showed a patchy or granular distribution within the supranuclear region of these cells. Intra- and subepithelial macrophages exhibited a weak TRAP, but no NOS-I or SOD, immune reaction. On the basis of the immunocytochemical findings, arguments in favor of a cytotoxic function of the superficial cells of the human urothelium are presented.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 286 (1996), S. 93-102 
    ISSN: 1432-0878
    Keywords: Key words: Microvasculature ; Fenestrated capillaries ; Lamina propria ; Testis ; Human
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. The three capillary parts of the microvasculature of the human testis, namely the arterial side inter-Leydig cell capillaries, the intramural capillaries, and the venous side inter-Leydig cell capillaries, were studied in detail by dual detection of alkaline phosphatase enzyme activity and endothelial marker immunoreactivity, and by means of light- and transmission-electron microscopy. Alkaline phosphatase enzyme activity was seen in intertubular arterioles, capillaries, and venules, and in intramural capillaries of the human testis, whereas the lamina propria of human seminiferous tubules showed no staining. Alkaline phosphatase enzyme activity and the endothelial marker detected by the Qbend 30 antibody co-existed within the endothelial cells of the microvasculature. Electron-microscopically, the endothelial cells of the arterial and venous side inter-Leydig cell capillaries, and of the intertubular capillaries free of Leydig cells were of the continuous type without fenestrations (A-1-α type). The intramural capillaries consisted of non-fenestrated (A-1-α type) and fenestrated sections (A-2-α type). The fenestrations faced the germinal epithelium. Capillaries with a continuous non-fenestrated endothelium contained a large number of transcytotic vesicles and channels. These were numerous in the endothelial cells of the inter-Leydig cell capillaries and the non-fenestrated part of the intramural capillaries. Capillaries partly ran in between the layers of the lamina propria and therefore represented the capillarization of the seminiferous tubules. Thus the multilayered lamina propria probably requires its own capillary supply to allow rapid exchange between the microvasculature and the epithelium of the human seminiferous tubules.
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  • 5
    ISSN: 1432-0878
    Keywords: Key words: NO/cGMP pathway ; Testis ; Leydig cells ; Immunocytochemistry ; RIA ; Cell culture ; Human
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. In this study we sought to determine whether the main components of the nitric oxide (NO) pathway are localized within the Leydig cells of the human testis and whether the soluble guanylyl cyclase (sGC), the enzyme that accounts for NO effects, is functionally active in these cells. Using an amplified immunocytochemical technique, immunoreactivity for nitric oxide synthase (NOS-I), sGC and cyclic guanosine monophosphate (cGMP) was detected within the cytoplasm of human Leydig cells. Distinct differences in staining intensity were found between individual Leydig cells, between cell groups and between Leydig cells of different patients. By means of a specific cGMP-RIA, a concentration-dependent increase in the quantity of cGMP was measured in primary cultures of human Leydig cells following exposure to the NO donor sodium nitroprusside. In addition, NOS-I immunoreactivity was seen in Sertoli cells, whereas cGMP and sGC immunoreactivity was found in Sertoli cells, some apically situated spermatids and residual bodies of seminiferous tubules. Dual-labelling studies and the staining of consecutive sections showed that there are several populations of Leydig cells in the human testis. Most cells were immunoreactive for NOS-I, sGC and cGMP, but smaller numbers of cells were unlabelled by any of the antibodies used, or labelled for NOS-I or cGMP alone, for sGC and cGMP, or for NOS-I and sGC. These results show that the Leydig cells possess both the enzyme by which NO is produced and the active enzyme which mediates the NO effects. There are different Leydig cell populations that probably reflect variations in their functional (steroidogenic) activity.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 175 (1976), S. 1-15 
    ISSN: 1432-0878
    Keywords: Rete testis ; Human ; Epithelial cell types ; Smooth muscle cells ; Histophysiology ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The ultrastructure of the normal human rete testis was analyzed. The rete testis cavities are irregularly shaped and contain virtually no spermatozoa. Smooth muscle cells often surround the cavities. In the epithelial lining, two cell types are distinguishable. Flat, dark cells exhibit numerous slender microvilli, and numerous apical and basal microvesicles. Prismatic, lighter cells have more cell organelles, mostly polarized towards a supranuclear position. Both cell types contain variable amounts of glycogen and fat, and an occasional cilium. All cells display intricate lateral cell surfaces that possess different cell-to-cell attachment devices. Intermediate cell types are frequently found. On a morphological basis, the epithelial cells seem to be involved in the release of substances into the lumen and probably also in transport towards the base. Connective tissue elements are found subjacent to the epithelium. Scattered among the fibrocytes are typical smooth muscle cells. Expansions of some smooth muscle cells are connected to the epithelial basement membrane by a network of microfibrillar material. The smooth muscle cells may be involved in changing the shape of the rete testis channels, thus promoting the flux of the rete testis fluid. Different types of nerve fibre bundles are distinguished in the connective tissue of the rete testis which may correspond to autonomic and sensory nerves or sensory receptors.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 189 (1978), S. 409-433 
    ISSN: 1432-0878
    Keywords: Rete testis ; Human ; Histophysiology ; Chordae retis ; Scanning electron microscopy ; Transmission electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The human rete testis was examined with regard to 1) the number and distribution of entrances of seminiferous tubules, 2) the light microscopic topography and 3) details of the passages as revealed by scanning and transmission electron microscopy. In a newborn 1474 entrances were counted, approximately 50 % entering from the right and 50 % from the left of the central long axis. Three major subdivisions of the rete were distinguished and described: a septal (or interlobular) part represented by tubuli recti, a tunical (or mediastinal) part which is a true network of channels, and an extratesticular part characterized by dilatations (up to 3 mm wide) which we have called bullae retis. In SEM, cylindrical strands running from wall to wall in the tunical and extratesticular rete spaces are a prominent feature. We have called these chordae retis. They are covered by epithelium and are 5–40 μm wide and 15 to more than 100 μm long. They contain a peculiar tissue consisting of central myoid cells in a fibroelastic matrix. The smaller chordae are avascular. In the light of these findings the rete is interpreted as a highly complex myoelastic sponge. Its function is discussed.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 192 (1978), S. 359-361 
    ISSN: 1432-0878
    Keywords: Spermatids ; Human ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Osmiophilic granules with surrounding vesicles resembling flower-like structures occur transiently during the differentiation of human spermatids. These organelles are incorporated into the residual bodies when mature spermatids are released from the germinal epithelium.
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