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  • 1
    In: Journal of Cancer Research and Clinical Oncology, Springer Science and Business Media LLC, Vol. 117, No. 6 ( 1991-11), p. S61-S83
    Type of Medium: Online Resource
    ISSN: 0171-5216 , 1432-1335
    RVK:
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 1991
    detail.hit.zdb_id: 134792-5
    detail.hit.zdb_id: 1459285-X
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  • 2
    Online Resource
    Online Resource
    The American Association of Immunologists ; 1985
    In:  The Journal of Immunology Vol. 135, No. 4 ( 1985-10-01), p. 2368-2373
    In: The Journal of Immunology, The American Association of Immunologists, Vol. 135, No. 4 ( 1985-10-01), p. 2368-2373
    Abstract: The effect of long-term topical application of corticosteroids on human cutaneous mast cells was examined. Two potent corticosteroids, clobetasol-17-propionate and fluocinonide, produced a greater than 85% decrease in histamine content over a 6-wk treatment period, whereas betamethasone valerate, a less potent corticosteroid, produced a 66% decrease. Electron microscopic examination of the biopsies taken from sites after 6 wk of treatment indicate that the reduced levels of histamine were caused by the depletion of mast cells, as evidenced by: the inability to identify any cells representative of mast cells by detailed electron microscopy of the biopsies; and the marked acellularity around the vasculature where mast cells are certain to be detected. Histamine levels did not begin to decline until after 3 wk of corticosteroid treatment, indicating that corticosteroids are not immediately harmful to mast cells. Electron microscopic examination of biopsies taken at the beginning of treatment and 1 wk later showed normal-appearing mast cells, whereas at 3 wk, a small population of mast cells was detected with features usually associated with degenerating or dying cells. These observations suggest that protracted application of corticosteroids to skin is toxic to mast cells. After discontinuation of treatment, the drug-related atrophy associated with chronic application of potent corticosteroids to skin is rapidly reversed, and skin structure returns to near normal by 14 days. Over this time period, however, histamine levels did not increase and mature mast cells could not be observed by electron microscopy. At 14 days post-steroid treatment, the first signs of cells containing sparse amounts of granules having the characteristics of mast cell granules were seen. We interpret this to represent new mast cells beginning to mature in the skin. By 3 mo, histamine levels returned to normal, demonstrating the reversibility of the steroid-induced mast cell depletion. The studies presented here establish the deleterious effects of long-term topical corticosteroid treatment on cutaneous mast cells, and begin to establish a system in which the development of mast cells in tissue can be investigated.
    Type of Medium: Online Resource
    ISSN: 0022-1767 , 1550-6606
    RVK:
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    Language: English
    Publisher: The American Association of Immunologists
    Publication Date: 1985
    detail.hit.zdb_id: 1475085-5
    detail.hit.zdb_id: 3056-9
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  • 3
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 1980
    In:  Journal of Gerontology Vol. 35, No. 3 ( 1980-05-01), p. 348-354
    In: Journal of Gerontology, Oxford University Press (OUP), Vol. 35, No. 3 ( 1980-05-01), p. 348-354
    Type of Medium: Online Resource
    ISSN: 0022-1422
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 1980
    detail.hit.zdb_id: 80138-0
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  • 4
    Online Resource
    Online Resource
    Wiley ; 1991
    In:  Journal of Cutaneous Pathology Vol. 18, No. 5 ( 1991-10), p. 309-314
    In: Journal of Cutaneous Pathology, Wiley, Vol. 18, No. 5 ( 1991-10), p. 309-314
    Abstract: Recent observations indicate that stem cells of the murine hair follicle exist exclusively as a subpopulation of relatively undiffer‐entiated outer root sheath cells located in the bulge region at the mid‐portion of the follicle. Because it has been hypothesized that stem cells of interfollicular epidermis may represent targets of cytotoxic responses in acute graft‐versus‐host disease (AGVHD), we studied murine AGVHD and observed sequential skin biopsies for the presence and evolutionary pattern of follicular injury. Highly purified subsets of donor T cells were used to produce AGVHD to multiple minor histocompatibility (H) antigens in two strain combinations of mice matched for the major histocompatibility complex (MHC). In the C3H.SW‐ 〉 B6 strain combination, only CD8+ effector cells produced histologic evidence in skin of AGVHD, which peaked three weeks post‐transplant. In the B10.D2‐ 〉 DBA/2 strain combination, CD4 + effector cells, and to a lesser extent, GD8 + cells, mediated disease, which peaked during the fourth week posttransplant. Analysis of skin from both strain/effector cell combinations revealed follicular infiltrates preferentially involving follicular stem cell (FSC) regions (bulge) of anagen follicles between the second and third weeks post‐transplant. These infiltrates often preceded infiltration of adjacent interfollicular epidermis and were associated with follicular involution to telogen (resting) phase. By the fourth week post‐transplant, 〉 50% of follicles were in telogen phase and residual inflammation was minimal. This provided a unique opportunity to observe follicular recovery from telogen. This involved formation of buds of premordial hair matrix derived from FSC populations of the bulge regions, and subsequent descent of these buds, initially tethered by elongate columns of putative stem cell progeny, along the course of fibrous tracts corresponding to follicular sheaths. These findings suggest that stem cells of hair follicles, as well as epidermis, represent potential targets of cytotoxicity in AGVHD. Moreover, they provide in vivo demonstration that the newly‐described FSC population of the follicular bulge give rise to germinative matrix epithelium upon pathological stimulation.
    Type of Medium: Online Resource
    ISSN: 0303-6987 , 1600-0560
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 1991
    detail.hit.zdb_id: 2018100-0
    detail.hit.zdb_id: 187078-6
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  • 5
    Online Resource
    Online Resource
    Proceedings of the National Academy of Sciences ; 1989
    In:  Proceedings of the National Academy of Sciences Vol. 86, No. 22 ( 1989-11), p. 8972-8976
    In: Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 86, No. 22 ( 1989-11), p. 8972-8976
    Abstract: To understand better the role of mast cell secretory products in the genesis of inflammation, a system was developed for in vitro degranulation of human mast cells in skin organ cultures. Within 2 hr after morphine sulfate-induced degranulation, endothelial cells lining microvessels adjacent to affected mast cells expressed an activation antigen important for endothelial-leukocyte adhesion. Identical results were obtained when other mast cell secretagogues (anti-IgE, compound 48/80, and calcium ionophore A23187) were used. Induction of this antigen was abrogated by preincubation with cromolyn sodium, an inhibitor of mast cell secretion, and by antiserum to tumor necrosis factor alpha. These findings indicate that degranulation of mast cells activates dermal endothelium through tumor necrosis factor-dependent mechanisms. This event may be critical to the elicitation phase of cutaneous inflammation.
    Type of Medium: Online Resource
    ISSN: 0027-8424 , 1091-6490
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    Language: English
    Publisher: Proceedings of the National Academy of Sciences
    Publication Date: 1989
    detail.hit.zdb_id: 209104-5
    detail.hit.zdb_id: 1461794-8
    SSG: 11
    SSG: 12
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  • 6
    Online Resource
    Online Resource
    The American Association of Immunologists ; 1986
    In:  The Journal of Immunology Vol. 137, No. 3 ( 1986-08-01), p. 962-970
    In: The Journal of Immunology, The American Association of Immunologists, Vol. 137, No. 3 ( 1986-08-01), p. 962-970
    Abstract: An antiserum was produced against a chymotryptic proteinase purified from human skin. The antiserum did not cross-react with human leukocyte cathepsin G and elastase, rat mast cell proteinase I, and human skin tryptase. Indirect immunofluorescent staining of frozen skin sections to localize the proteinase showed cytoplasmic staining of cells scattered about the papillary dermis and around blood vessels and appendages. Restaining these sections with toluidine blue revealed that the fluorescently stained cells contained metachromatically staining granules, the major distinguishing feature of mast cells. A similar correlation was found in lung tissue. Ultrastructural studies employing the ferritin bridge technique to immunologically identify the proteinase additionally localized the proteinase to mast cell granules. Biochemical and immunochemical characterization of chymotryptic activity solubilized from isolated human lung mast cells identified a chymotryptic proteinase that may be identical to the skin chymotryptic proteinase. These studies establish that human skin mast cells contain a chymotrypsin-like proteinase that is a granule constituent and provide evidence that indicates a comparable proteinase is also present in lung mast cells.
    Type of Medium: Online Resource
    ISSN: 0022-1767 , 1550-6606
    RVK:
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    Language: English
    Publisher: The American Association of Immunologists
    Publication Date: 1986
    detail.hit.zdb_id: 1475085-5
    detail.hit.zdb_id: 3056-9
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  • 7
    Online Resource
    Online Resource
    Wiley ; 1987
    In:  Journal of Cutaneous Pathology Vol. 14, No. 5 ( 1987-10), p. 291-298
    In: Journal of Cutaneous Pathology, Wiley, Vol. 14, No. 5 ( 1987-10), p. 291-298
    Abstract: Cowden's disease is characterized by multiple hamartomas of the skin, breast, thyroid, and gastrointestinal tract. In the past, a viral hypothesis for the keratotic lesions of the skin has led to much controversy. The present study describes the results of a detailed fine structural analysis of 10 hyperkeratotic extremity lesions and 2 keratotic lesions from the face of a patient with Cowden's disease. Increases in the keratinocyte population were primarily confined to the basal and suprabasal regions. Differentiation products characteristic of keratinization were normal in both quantity and appearance. Nuclear remnants and number‐ous lipid droplets, markers of abnormal keratinization, were noted within horny cells. However, viral particles and/or virus‐like particles were not observed in keratinocytes. Melanocytes and Langerhans cells were numerous. The latter contained membrane‐bound pigment vacuoles in addition to the characteristic Birbeck granules. These unusual Langerhans cells were observed in the dermis as well as the epidermis. A large number of fully granulated ‘resting” mast cells was uniformly distributed throughout the dermis, associated with a prominent cellular infiltrate. Our observations do not support the concept of a viral etiology for these tumors.
    Type of Medium: Online Resource
    ISSN: 0303-6987 , 1600-0560
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 1987
    detail.hit.zdb_id: 2018100-0
    detail.hit.zdb_id: 187078-6
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  • 8
    Online Resource
    Online Resource
    American Society for Microbiology ; 1995
    In:  Clinical Diagnostic Laboratory Immunology Vol. 2, No. 3 ( 1995-05), p. 297-301
    In: Clinical Diagnostic Laboratory Immunology, American Society for Microbiology, Vol. 2, No. 3 ( 1995-05), p. 297-301
    Abstract: Previous studies have identified two ultrastructurally distinct forms of mast cell (MC) degranulation following activation. Immunoglobulin E (IgE)-mediated reactions are characterized by a very rapid swelling and fusion of MC granules and abrupt mediator release. In certain chronic disease states (e.g., bullous pemphigoid), there is "piecemeal" degranulation with a more-gradual mediator release effected by microvesicular transport of "pieces" of granules to the cell surface. It is unclear whether these two degranulation patterns are determined by the different natures of the stimuli, heterogeneity among responding MC granules, or temporal factors. To investigate these issues, we have carried out electron microscopic studies with skin biopsies obtained from ragweed-sensitive subjects 15 and 30 s and 1, 3, 5, and 10 min after intradermal ragweed injection. "Anaphylactic"-type granule changes began by 15 s after ragweed injection and were complete by 5 min; unaffected granules were juxtaposed with granules that were swollen and fused. The remaining granules subsequently underwent changes in appearance similar to those seen in piecemeal degranulation. However, microvesicular transport of granule components to the surface was not observed. These findings indicate that skin MC changes in sites of IgE-mediated reactions include not only the typical very rapid anaphylactic degranulation but also a slower onset of gradual alteration of other granules, frequently within the same MC. These different patterns could reflect MC granule heterogeneity with attendant different responses to IgE-mediated stimuli.
    Type of Medium: Online Resource
    ISSN: 1071-412X , 1098-6588
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 1995
    detail.hit.zdb_id: 1496863-0
    detail.hit.zdb_id: 1193675-7
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  • 9
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 1985
    In:  British Journal of Dermatology Vol. 112, No. 2 ( 1985-02), p. 185-193
    In: British Journal of Dermatology, Oxford University Press (OUP), Vol. 112, No. 2 ( 1985-02), p. 185-193
    Type of Medium: Online Resource
    ISSN: 0007-0963 , 1365-2133
    URL: Issue
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 1985
    detail.hit.zdb_id: 80076-4
    detail.hit.zdb_id: 2004086-6
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  • 10
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2003
    In:  Eye Vol. 17, No. 8 ( 2003-11), p. 937-942
    In: Eye, Springer Science and Business Media LLC, Vol. 17, No. 8 ( 2003-11), p. 937-942
    Type of Medium: Online Resource
    ISSN: 0950-222X , 1476-5454
    RVK:
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    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2003
    detail.hit.zdb_id: 2080338-2
    detail.hit.zdb_id: 91001-6
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