FULL-THICKNESS HUMAN SKIN EXPLANTS FOR TESTING THE TOXICITY OF TOPICALLY APPLIED CHEMICALS

被引:38
|
作者
NAKAMURA, M
RIKIMARU, T
YANO, T
MOORE, KG
PULA, PJ
SCHOFIELD, BH
DANNENBERG, AM
机构
[1] JOHNS HOPKINS UNIV,SCH HYG,DEPT ENVIRONM HLTH SCI,615 N WOLFE ST,BALTIMORE,MD 21205
[2] JOHNS HOPKINS UNIV,SCH HYG,DEPT EPIDEMIOL,BALTIMORE,MD 21205
[3] JOHNS HOPKINS UNIV,SCH HYG,DEPT IMMUNOL & INFECT DIS,BALTIMORE,MD 21205
[4] JOHNS HOPKINS UNIV,SCH MED,DEPT PATHOL,BALTIMORE,MD 21205
[5] JOHNS HOPKINS UNIV,SCH MED,DEPT DERMATOL,BALTIMORE,MD 21205
关键词
D O I
10.1111/1523-1747.ep12485073
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
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°C. In the 0.03-1.0% dosage range, a straightline 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°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°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. © 1990.
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页码:325 / 332
页数:8
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