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  • 1
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2000
    In:  Advances in Therapy Vol. 17, No. 1 ( 2000-1), p. 7-13
    In: Advances in Therapy, Springer Science and Business Media LLC, Vol. 17, No. 1 ( 2000-1), p. 7-13
    Type of Medium: Online Resource
    ISSN: 0741-238X , 1865-8652
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2000
    detail.hit.zdb_id: 2421646-X
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  • 2
    Online Resource
    Online Resource
    Microbiology Society ; 2002
    In:  Journal of General Virology Vol. 83, No. 7 ( 2002-07-01), p. 1579-1590
    In: Journal of General Virology, Microbiology Society, Vol. 83, No. 7 ( 2002-07-01), p. 1579-1590
    Abstract: Herpetic stromal keratitis (HSK) and blepharoconjunctivitis in humans are thought partly to result from immunopathological responses to herpes simplex virus type 1 (HSV-1). The corneas of NIH mice were inoculated with HSV-1 (strain McKrae) and mice were examined for signs of disease and infection on days 1, 4, 7, 10, 14 and 21. The eyes and eyelids of infected and control mice were processed for immunohistochemistry and double stained for viral antigens and one of the following cell surface markers (Gr-1, F4/80, CD4, CD8, CD45R or MHC class II) or one of the following cytokines (IL-2, IL-4, IL-6, IL-10, IL-12 or IFN-γ). All infected mice developed signs of HSK by day 4 and blepharitis by day 7 and these both persisted until day 21, when signs of resolution where apparent. Virus was detected during the first week of infection and became undetectable by day 10. Large numbers of Gr-1 + cells (neutrophils) infiltrated infected corneas and eyelids in areas of viral antigen and CD4 + T cells increased significantly in number after virus clearance. In both sites, the predominant cytokines were IL-6, IL-10, IL-12 and IFN-γ, with few IL-2 + and IL-4 + cells. These observations suggest that the immune responses in the cornea are similar to those in the eyelids but, overall, the responses are not clearly characterized as either Th1 or Th2. In both sites, the neutrophil is the predominant infiltrating cell type and is a likely source of the cytokines observed and a major effector of the disease process.
    Type of Medium: Online Resource
    ISSN: 0022-1317 , 1465-2099
    RVK:
    RVK:
    Language: English
    Publisher: Microbiology Society
    Publication Date: 2002
    detail.hit.zdb_id: 2007065-2
    SSG: 12
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  • 3
    In: FEBS Letters, Wiley, Vol. 529, No. 2-3 ( 2002-10-09), p. 281-285
    Abstract: C‐terminal domain tissue inhibitor of metalloproteinases‐3 (TIMP‐3) mutations cause the rare hereditary blindness Sorsby's fundus dystrophy (SFD), which involves loss of retinal pigment epithelial (RPE) cells. Since wild‐type TIMP‐3 causes apoptosis, we investigated whether SFD TIMP‐3 might kill RPE and other cells. Plasmid‐mediated overexpresion of Ser‐156, Gly‐167, Tyr‐168 and Ser‐181 SFD mutant TIMP‐3 decreased RPE viability to 22±8, 20±6, 32±5, 30±12% (SFD mutants all P 〈 0.01 versus wild‐type 50±8%) and similarly increased propidium iodide staining and in situ end labelling. Adenovirus‐mediated overexpression of the Gly‐167 mutant also caused RPE apoptosis dose‐dependently. Apoptosis of RPE cells might therefore contribute to the pathology of SFD.
    Type of Medium: Online Resource
    ISSN: 0014-5793 , 1873-3468
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2002
    detail.hit.zdb_id: 1460391-3
    SSG: 12
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  • 4
    Online Resource
    Online Resource
    S. Karger AG ; 2001
    In:  Ophthalmic Research Vol. 33, No. 1 ( 2001), p. 1-6
    In: Ophthalmic Research, S. Karger AG, Vol. 33, No. 1 ( 2001), p. 1-6
    Abstract: 〈 i 〉 Purpose: 〈 /i 〉 Corneas that are maintained in tissue culture medium shed their epithelial cells and repopulation following graft surgery is an essential facet of the healing process. Failure to do so may be a result of structural damage to the epithelial basement membrane of a donor cornea. The purpose of the present investigation was to ascertain whether MMP-2, the matrix metalloproteinase produced by corneal keratocytes, may be activated during storage and hence cleave the type IV collagen component of the epithelial cell basement membrane. 〈 i 〉 Methods: 〈 /i 〉 Fresh and transplant rejected corneas that had been stored in culture medium for varying time periods and of known donor age were collected. The soluble protein fractions of these corneas were obtained. Their MMP-2 proteins were visualised by zymography on SDS gelatin polyacrylamide gels and assayed for activity against nitrophenyl acetate and denatured [ 〈 sup 〉 3 〈 /sup 〉 H]type I collagen. 〈 i 〉 Results: 〈 /i 〉 The stromal tissue of fresh, normal corneas produced inactive MMP-2 of M 〈 sub 〉 r 〈 /sub 〉 66,000. Although the cultured corneas did not up-regulate MMP-2 production, they contained additional MMP-2 activities of M 〈 sub 〉 r 〈 /sub 〉 62,000 and M 〈 sub 〉 r 〈 /sub 〉 43,000. The appearance of these additional MMP-2 activities correlated with corneal culture time but not donor age. The ability to cleave denatured [ 〈 sup 〉 3 〈 /sup 〉 H]type I collagen correlated with the appearance of the M 〈 sub 〉 r 〈 /sub 〉 43,000 activity but not the M 〈 sub 〉 r 〈 /sub 〉 62,000 activity. 〈 i 〉 Conclusion: 〈 /i 〉 Activated MMP-2 is produced in cultured corneas. For this reason the corneas donated for all graft procedures should not be held in culture medium for periods exceeding 4 weeks.
    Type of Medium: Online Resource
    ISSN: 0030-3747 , 1423-0259
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2001
    detail.hit.zdb_id: 1483177-6
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