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

Authors: Nakamura, M; Rikimaru, T; Yano, T; Moore, K G; Pula, P J; Schofield, B H; Dannenberg Jr, A M

Published In J Invest Dermatol, (1990 Sep)

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.

PubMed ID: 2384690

MeSH Terms: Administration, Topical; Azides/pharmacology; Carbon Radioisotopes; Cycloheximide/pharmacology; Dose-Response Relationship, Drug; Humans; Leucine/metabolism; Mustard Compounds/toxicity*; Mustard Gas/administration & dosage; Mustard Gas/toxicity*; Organ Culture Techniques; Protein Biosynthesis; Skin/drug effects*; Skin/ultrastructure; Temperature; Tissue Survival/drug effects; Vacuoles/drug effects