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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    BJOG 93 (1986), S. 0 
    ISSN: 1471-0528
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Summary. A morphometric analysis was performed of the Langerhans' cell density in epithelial sheets obtained from normal exocervices and from exocervices with squamous carcinoma. Laminae of exocervices with squamous carcinoma that showed cervical intraepithelial neoplasia (CIN) were classified according to its predominant degree of severity as CIN I, CIN II and CIN III or as normal when no neoplastic changes were found. Laminae with CIN showed a higher Langerhans' cell density than the laminae from normal exocervices and than the normal laminae of exocervices with carcinoma. The magnitude of the increase of Langerhans' cell density and the degree of severity of the neoplastic changes appear as closely related phenomena. An increase of the more ramified types of Langerhans' cell in the laminae containing CIN was found, with the most ramified being more frequent in the most severe lesions.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Ultrasructure Research 65 (1978), S. 279-295 
    ISSN: 0022-5320
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-069X
    Keywords: Langerhans cell ; Contact dermatitis ; Antigen processing ; 2,4-Dinitrofluorobenzene ; Antigen-presenting cell
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The cellular and subcellular distribution of 2,4-dinitrophenyl (DNP) groups in the epidermis and regional lymph nodes of the mouse was investigated after epicutaneous application of 2,4-dinitrofluorobenzene (DNFB) to sensitized and non-sensitized mice. The peroxidase-antiperoxidase method and the immunogold technique were used to visualize the DNP groups at both light and electron microscopic levels. The highest intensity of immunolabelling was found on tonofilaments of keratinocytes present in the upper layers of the epidermis. On the other hand, in vitro experiments showed that DNFB has the capacity to bind keratin which, together with immunocytochemistry, suggests that this molecule may be one of the skin protein carriers for DNFB. In addition, intense immunostaining for DNP was observed in the Golgi area of some epidermal Langerhans cells. Cells immunoreactive to DNP were also observed in the marginal sinus of cervical lymph nodes 6, 12 and 24 h after challenge. Immunoelectron microscopy revealed immunoreactive DNP groups in phagosomes of Langerhans cells at this site. The present findings support the hypothesis that the hapten DNFB penetrates passively into the cytoplasm of Langerhans cells, concentrates in the Golgi area and, during the migration of Langerhans cells to the lymph nodes, it is probably processed in the lysosomes before its presentation to T lymphocytes.
    Type of Medium: Electronic Resource
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