Literature DB >> 2384690

Full-thickness human skin explants for testing the toxicity of topically applied chemicals.

M Nakamura1, T Rikimaru, T Yano, K G Moore, P J Pula, B H Schofield, A M Dannenberg.   

Abstract

This report describes a model organ-culture system for testing the toxicity of chemical substances that are topically applied to human skin. In this system, the viable keratinocytes in the full-thickness skin explants are protected by the same keratinized layer as skin remaining on the donor, and toxicity can be assessed microscopically and/or biochemically. The human skin specimens were discards from a variety of surgical procedures. They were cut into full-thickness 1.0-cm2 explants, and briefly exposed to the military vesicant sulfur mustard (SM), which was used as a model toxicant. The explants were then organ cultured in small Petri dishes for 24 h at 36 degrees C. In the 0.03-1.0% dosage range, a straight-line dose-response relationship occurred between the concentration of SM applied and the number of paranuclear vacuoles seen histologically in the epidermis. Within the same SM dosage range, there was also a proportional decrease in 14C-leucine incorporation by the explants. Thus, the number of paranuclear vacuoles reflected decreases in protein synthesis by the injured epidermal cells. The epidermis of full-thickness untreated (control) human skin explants usually remained viable for 7 d when stored at 4 degrees C in culture medium. During storage, a relatively small number of paranuclear vacuoles developed within the epidermis, but the explants were still quite satisfactory for testing SM toxicity. Incubation (for 4 or 24 h at 36 degrees C) of such control skin explants reduced (often by 50%) the small number of paranuclear vacuoles produced during 4-7 d of storage. This reduction was probably caused by autolysis of many of the vacuolated cells. Two types of paranuclear vacuoles could be identified by both light and electron microscopy: a storage type and a toxicant type. The storage type seemed to be caused by autolysis of cell components. The toxicant type seemed to be caused by an invagination of the plasma membrane. Only toxicant-type vacuoles increased appreciably in number when skin explants were exposed to mustard, and to other toxicants.

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Year:  1990        PMID: 2384690     DOI: 10.1111/1523-1747.ep12485073

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  9 in total

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2.  Role of MAP kinases in regulating expression of antioxidants and inflammatory mediators in mouse keratinocytes following exposure to the half mustard, 2-chloroethyl ethyl sulfide.

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Journal:  Toxicol Appl Pharmacol       Date:  2010-04-09       Impact factor: 4.219

3.  [Effects of emulsions on the stratum corneum barrier and hydration].

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Authors:  Scott A Reisman; Angela R Goldsberry; Chun-Yue I Lee; Megan L O'Grady; Joel W Proksch; Keith W Ward; Colin J Meyer
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Authors:  Dora E Corzo-León; Carol A Munro; Donna M MacCallum
Journal:  Front Microbiol       Date:  2019-06-05       Impact factor: 5.640

Review 8.  Interrupting Neuron-Tumor Interactions to Overcome Treatment Resistance.

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Journal:  Cancers (Basel)       Date:  2020-12-12       Impact factor: 6.639

9.  Active neutrophil responses counteract Candida albicans burn wound infection of ex vivo human skin explants.

Authors:  Christin von Müller; Fionnuala Bulman; Lysett Wagner; Daniel Rosenberger; Alessandra Marolda; Oliver Kurzai; Petra Eißmann; Ilse D Jacobsen; Birgit Perner; Peter Hemmerich; Slavena Vylkova
Journal:  Sci Rep       Date:  2020-12-11       Impact factor: 4.379

  9 in total

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