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  • 1
    ISSN: 1439-0973
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Untersuchungen zur Wechselwirkung zwischenNeisseria gonorrhoeae und menschlicher Tubenschleimhaut in Organkultur lassen annehmen, daß das Anheften der Gonokokken den Erreger im Wirtsorganismus schützt und außerdem den Krankheitsprozeß in Gang setzt. In Organkulturen von Tubengewebe lassen sich folgende Schritte der Gonokokkeninfektion beobachten: 1) Die Gonokokken lagern sich an die Microvilli zilienfreier Zellen an; 2) Gonokokken setzen Lipopolysaccharide und möglicherweise auch andere toxische Verbindungen frei, die die Schleimhaut schädigen; 3) zilienfreie Zellen verschlingen oder phagozytieren Gonokokken; 4) phagozytäre Vakuolen mit Gonokokken werden an die Basis der zilienfreien Zellen transportiert; 5) Gonokokken in den phagozytären Vakuolen treten in das subepitheliale Gewebe aus.In vivo könnten diese Vorgänge zu einem ausgedehnten, lokalisierten Krankheitsprozeß (beispielsweise einer Salpingitis) führen oder zur Invasion in Blutgefäße mit disseminierter Erkrankung. Frühere Untersuchungen anN. meningitidis-infiziertem menschlichen Nasopharyngealgewebe zeigen, daß Meningokokken sich an Microvilli nichtzilientragender Zellen anheften und von diesen Zellen phagozytiert werden. Anschließend erscheinen Meningokokken im subepithelialen Gewebe; der Weg der Ausbreitung ist allerdings noch ungewiß. Aus diesen Beobachtungen lassen sich zumindest einige der Vorgänge ableiten, über die Adhäsion in der Pathogenese von Gonokokken- und Meningokokkenerkrankungen eine Rolle spielt. Mechanismen, die das Anheften der Bakterien verhindern, bieten möglicherweise neue Ansätze für die Prävention von Erkrankungen, die durch pathogene Neisserien verursacht werden.
    Notes: Summary Studies of the interaction betweenNeisseria gonorrhoeae and human fallopian tube mucosa in organ culture suggest that attachment of gonococci is important, not only to secure the organism in the host, but also to initiate the disease process. The steps observed in gonococcal infection of fallopian tube organ cultures are: 1) attachment of gonococci to microvilli of nonciliated cells; 2) release from gonococci of lipopolysaccharide and possibly other toxic moities to cause mucosa damage; 3) engulfment or phagocytosis of gonococci by nonciliated cells; 4) transport of phagocytic vacuoles containing gonococci to the base of the nonciliated cells; and 5) exocytosis of gonococci within phagocytic vacuoles into the subepithelial tissues.In vivo, these steps might result in extensive local disease (e. g. salpingitis) or in the invasion of blood vessels to cause disseminated disease. Preliminary studies of human nasopharyngeal tissue in organ culture infected withNeisseria meningitidis indicate that meningococci attach to microvilli of nonciliated cells and are phagocytized by these cells. Meningococci subsequently appear in subepithelial tissues, though the route they take is not yet certain. These observations suggest at least some of the ways in which attachment may play a role in disease caused byN. gonorrhoeae andN. meningitidis. Mechanisms to block this attachment may provide new approaches to the prevention of infections caused by the pathogenicNeisseria.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: A study of the progestational evolution of the endometrium of the rabbit in pseudopregnancy suggests a division into the following phases: (1) priming phase (0-24 hours), in which no significant changes were observed except for leucocytic invasion of the epithelium, (2) proliferative phase (1-4 days), in which mitosis is active and the epithelium becomes pseudostratified and the glands proliferate, (3) phase of epithelial relayering and folding (4-6 days), in which the epithelium is single-layered and there is evidence of secretory activity, (4) phase of cell fusion (6-8 days), in which the columnar cells fuse into multinucleated masses, and (5) maximally progestational phase (8-13 days), in which almost all the epithelial cells are multinucleated except for occasional ciliated cells, and, in some animals with evidence of the effects of high systemic levels of estrogen, extensive ciliation, especially antimesometrially. A final phase (6), not studied in detail, is a declining phase marked by degeneration and sloughing of the multinucleated epithelium and replacement with predominantly ciliated cells. Reconstruction of the minor mucosal folds, as distinct from the six or so major folds present in the non-pregnant animal, shows that these are true elevations of the mucosa above the level of the mouths of the glands. The current concept of progestational changes in the endometrium of the rabbit as predominantly due to glandular proliferation is incorrect; this has important implications for analysis of the implantation process.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The fine structure of the endometrial epithelium of the pseudopregnant rabbit from the day of induced ovulation (day 0) to the 13th day is here correlated with previously defined light microscopic phases. In Phase 1 (0-1 day), in which there is a presumed “priming” of the endometrium by ovarian steroidal hormones, no changes were observed. In Phase 2 (1-3 days), in addition to mitotic activity, the epithelium showed a disappearance of the mucification and lymphocytic migration typical of Phase 1 and also of the nonpregnant or “estrous” phase, and showed other nuclear and cytoplasmic changes which probably reflect endogenous growth and protein synthesis. In Phase 3 (4-6 days), two distinct populations of reacting cells were present: (1) surface and cryptal cells investing the now folded mucosal surface, and (2) glandular cells. The first group showed characteristic dome-like protrusions of the cytoplasm into the lumen, and also showed distinct cytoplasmic and nuclear changes which appear to be a prelude to the succeeding phase of fusion but are not necessarily secretory in type. The glandular cells, in contrast, showed cytoplasmic changes which appear to reflect active secretory activity (hypertrophy of the Golgi area, cytoplasmic vacuoles containing electron-opaque material, etc.). This phase coincides with the maximal secretion of uterine-specific proteins, and electron-opaque material is abundant within the endometrial lumen. In Phase 4 (6-8 days), the surface and cryptal epithelium undergoes a transformation into multinucleated cells, the result of a process of lysis of intervening plasma membranes, the precise mechanism of which (i.e., with or without initial membrane fusion) was not determined. Cell fusion proceeded earlier and more actively mesometrially than antimesometrially. The glandular cells showed evidence of reduced secretory activity, but did not at any stage undergo multinucleate-cell transformation. In Phase 5 (8-13 days) there was progressive fusion, and the number of nuclei per cytoplasmic sac appeared increased, presumably due to the continued action of progesterone which is maximal during this phase. Glandular cells showed further reduced secretory activity but remained columnar. Ciliation of the epithelium was sporadic in the pre-secretory phases and rare or absent in the secretory and fusion phases; it became widespread during the phase of decline after day 14, a period which will not be included in this study. The fine structure of the ciliated cells was the same at all stages; there was no evidence for their origin from a reserve population; it is possible that they arise by modification of the multinucleated cells. Cytoplasmic crystals and intramitochondrial densities or lamellae were observed during the secretory and fusion stages, the former only in the glands, the latter in the surface and cryptal epithelium. They appear to be associated with rising or maximal progesterone secretion.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 178 (1987), S. 326-334 
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Plasma membrane structure of bat spermatozoa was examined utilizing electron microscopy of thin sections and freeze-fracture replicas. Notable membrane features observed in replicas from cauda epididymal spermatozoa included specialized particle aggregates at the junction between the acrosomal and postacrosomal region of the head (a membrane structure not previously described in mammalian spermatozoa) and another row of rod-like particles just anterior to the posterior ring. Both of these specializations in fractured plasma membranes correspond with regions where the membrane is closely apposed to underlying structures when viewed in thin sections. The postacrosomal sheath appears to be composed of an array of longitudinally oriented filamentous components. Characteristic ordering of intramembranous particles was also noted in replicas from the midpiece region and the annulus. Major changes in plasma membrane structure were not seen in spermatozoa stored in the female reproductive tract; however, the appearance of linear particle aggregations in the principal piece membrane was noted. No evidence was obtained to suggest that an acrosome reaction had occurred in spermatozoa stored in females.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-0878
    Keywords: Key words Endometrium ; Blastocyst ; Implantation ; E-cadherin ; Cell fusion ; ADAM family ; Uterus ; Rabbit
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract  Blastocyst attachment to mammalian uteri at implantation involves the adhesion of the trophoblast to the uterine epithelial surface. In the rabbit, fusion between adjacent epithelial cells precedes the initial attachment phase and is followed by fusion between the trophoblast and the epithelium. The reverse transcription/polymerase chain reaction method has been used to prepare a partial cDNA (rbMDC9) from periimplantation-stage endometrium; this represents the rabbit ortholog of MDC9, a member of the cellular metalloproteinase/disintegrin (ADAM) gene family. We demonstrate here the reproductive stage-specific expression of rbMDC9 mRNA in uterine epithelium during the periimplantation period. Furthermore, this expression is upregulated at implantation sites, and in situ hybridization analysis has revealed that the epithelial cells with the most prominent signal are those apposed to blastocysts. Immunostaining with E-cadherin has been used to trace lateral membranes of epithelial cells and, together with nuclear staining, has enabled the identification of cells fusing to become multinucleated cells, and later, to become an epithelial syncytium (symplasma). These fusing cells express the highest level of rbMDC9 mRNA. The results suggest that MDC9, a transmembrane modular protein with domains having potential integrin-binding, metalloproteinase, and fusogenic functions, is probably critical for the cellular interactions accompanying blastocyst implantation.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 6 (1982), S. 161-178 
    ISSN: 0148-7280
    Keywords: epididymis ; epithelium ; ultrastructure ; lectin ; protein synthesis ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: An enriched suspension of rat epididymal epithelial cells was prepared by sequential enzymatic removal of connective tissue and peritubular cells from the epididymal tubule. The viability, structural characteristics, and pattern of polypeptides synthesized by the isolated cells were determined. Electron microscopic analysis revealed that the isolated principal cells were intact and retained their polarized morphology. Several light microscopic protocols were employed to evaluate the percentage of epithelial cells in the suspensions. These included (1) the visualization of the pattern of FITC-lectin binding in which the principal cells could be identified by their polarized fluorescence; (2) the visualization of prominent autofluorescent granules in the cell cytoplasm which appeared to be characteristic of only epithelial cells; and (3) immunochemical staining with an antikeratin antibody which was reactive only with cells of epithelial origin. These structural probes indicated that between 80% and 90% of the isolated cells were epithelial in nature. Two-dimensional gel electrophoresis revealed a complex pattern of polypeptides synthesized by the epithelial cells; these results are compared to those of earlier studies utilizing minced whole epididymis.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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