There is an important need in the study of toxicology of topically-applied and environmental agents for an in vitro system to study their toxic effects on skin. The in vitro systems have the benefit of allowing study of a large variety of substances on an individual specimen. An in vitro system containing all the components of skin allows studies to determine the effects of agents on the various component cell types and cell interactions. This is particularly the case in three-dimensional histoculture systems. The applicant developed a gel-supported, three-dimensional histoculture system that allows the intact growth and toxicity testing of all components of mouse skin, including keratinocytes, dermal fibroblasts and hair follicle cells as well as hair, for periods of 10 days or more (Li, L., Margolis, L.B. and Hoffman, R.M. Proc. Natl. Acad. Sci., In Press). It is proposed here, using the histoculture system and fluorescent dyes that measure cell viability or cell death, to investigate the effects of a series of pesticides, organotins and carcinogens as model compounds to study toxicity and carcinogenesis on all types of histocultured mouse skin and human foreskin as well as on hair growth from the cultured skin. The measurement of the effects of the toxins are greatly enhanced by confocal microscopy which allows the three-dimensional observation of the specimens not previously possible. The effects of at least one compound in vitro have already correlated in vivo using athymic nude mice such that the cytotoxic effects in vitro correspond to an irritation index for these various compounds scored in vivo.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Small Business Innovation Research Grants (SBIR) - Phase I (R43)
Project #
1R43CA053995-01A1
Application #
3492744
Study Section
Experimental Therapeutics Subcommittee 1 (ET)
Project Start
1991-09-15
Project End
1992-03-16
Budget Start
1991-09-15
Budget End
1992-03-16
Support Year
1
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Anticancer, Inc.
Department
Type
DUNS #
City
San Diego
State
CA
Country
United States
Zip Code
92111
Li, L; Hoffman, R M (1997) Topical liposome delivery of molecules to hair follicles in mice. J Dermatol Sci 14:101-8
Li, L; Hoffman, R M (1995) Model of selective gene therapy of hair growth: liposome targeting of the active Lac-Z gene to hair follicles of histocultured skin. In Vitro Cell Dev Biol Anim 31:11-3
Paus, R; Krejci-Papa, N; Li, L et al. (1994) Correlation of proteolytic activities of organ cultured intact mouse skin with defined hair cycle stages. J Dermatol Sci 7:202-9
Li, L; Lishko, V; Hoffman, R M (1993) Liposome targeting of high molecular weight DNA to the hair follicles of histocultured skin: a model for gene therapy of the hair growth processes. In Vitro Cell Dev Biol Anim 29A:258-60
Li, L; Lishko, V K; Hoffman, R M (1993) Liposomes can specifically target entrapped melanin to hair follicles in histocultured skin. In Vitro Cell Dev Biol 29A:192-4
Hoffman, R M (1993) Histoculture radiometric in vitro hair growth assay. In Vitro Cell Dev Biol Anim 29A:449-50
Li, L; Margolis, L B; Lishko, V K et al. (1992) Product-delivering liposomes specifically target hair follicles in histocultured intact skin. In Vitro Cell Dev Biol 28A:679-81
Li, L; Paus, R; Slominski, A et al. (1992) Skin histoculture assay for studying the hair cycle. In Vitro Cell Dev Biol 28A:695-8
Li, L; Paus, R; Margolis, L B et al. (1992) Hair growth in vitro from histocultured skin. In Vitro Cell Dev Biol 28A:479-81
Li, L; Margolis, L B; Paus, R et al. (1992) Hair shaft elongation, follicle growth, and spontaneous regression in long-term, gelatin sponge-supported histoculture of human scalp skin. Proc Natl Acad Sci U S A 89:8764-8