Analysis of interleukin-1α (IL-1α) and interleukin-8 (IL-8) expression and release in in vitro reconstructed human epidermis for the prediction of in vivo skin irritation and/or sensitization

被引:132
作者
Coquette, A
Berna, N
Vandenbosch, A
Rosdy, M
De Wever, B
Poumay, Y
机构
[1] SGS Biopharma S A, Dept Biol, B-1301 Wavre, Belgium
[2] Fac Univ Notre Dame Paix, Dept Histol & Embryol, B-5000 Namur, Belgium
[3] SkinEth Labs, F-06000 Nice, France
关键词
D O I
10.1016/S0887-2333(03)00019-5
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
In the present study, reconstructed human epidermis (RHE) was used as an in vitro model to discriminate 1-chloro-2,4-dinitrobenzene (DNCB), nickel sulfate (NiSO4) Oxazolone (OXA), 2,4-dinitrofluorobenzene (DNFB) and 2,4,6-trinitrobenzenesulfonic acid (TNBS) as skin sensitizers from benzalkonium chloride (BC), benzoic acid (BA) and sodium lauryl sulfate (SLS) as skin irritants. Our criteria were (a) the differential IL-1alpha and IL-8 synthesis and release (b) cytotoxicity assessment by MTT assay. When the RHE are topically treated with the sensitizers, very low levels of extra- and intracellular IL-1alpha are observed although they induce significant cytotoxicity. In contrast, they exhibit a sharp maximum of IL-8 release. In the presence of the tested irritants, we observe the inverse cytokine release profile, although they induce dose-dependent cytotoxicity profiles similar to those observed with the sensitizers. Finally, IL-1alpha mRNA upregulation is observed after topical application of both sensitizers and irritants, but only the latter significantly increase extracellular IL-1alpha. In conclusion, our results suggest that the associated determination of IL-8, with IL-1alpha, and MTT conversion are at least necessary to discriminate and classify, in a single assay, irritant and sensitizing agents and represent a potential in vitro alternative to two classical in vivo assays. (C) 2003 Elsevier Science Ltd. All rights reserved.
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页码:311 / 321
页数:11
相关论文
共 52 条
[1]  
AMGNUSSON B, 1970, ALLERGIC CONTACT DER
[2]   KERATINOCYTES AS INITIATORS OF INFLAMMATION [J].
BARKER, JNWN ;
MITRA, RS ;
GRIFFITHS, CEM ;
DIXIT, VM ;
NICKOLOFF, BJ .
LANCET, 1991, 337 (8735) :211-214
[3]   Use of the local lymph node assay for the estimation of relative contact allergenic potency [J].
Basketter, DA ;
Blaikie, L ;
Dearman, RJ ;
Kimber, I ;
Ryan, CA ;
Gerberick, GF ;
Harvey, P ;
Evans, P ;
White, IR ;
Rycroft, RJG .
CONTACT DERMATITIS, 2000, 42 (06) :344-348
[4]  
BASKETTER DA, 1999, CLIN DERMATOL, V15, P637
[5]   THE LIVING SKIN EQUIVALENT - ITS MANUFACTURE, ITS ORGANOTYPIC PROPERTIES AND ITS RESPONSES TO IRRITANTS [J].
BELL, E ;
PARENTEAU, N ;
GAY, R ;
NOLTE, C ;
KEMP, P ;
BILBO, P ;
EKSTEIN, B ;
JOHNSON, E .
TOXICOLOGY IN VITRO, 1991, 5 (5-6) :591-596
[6]  
Berardesca E, 1995, Curr Probl Dermatol, V23, P1
[7]  
Bernard F.-X., 2000, International Journal of Cosmetic Science, V22, P397, DOI 10.1046/j.1467-2494.2000.00035.x
[8]   Development of a highly sensitive in vitro phototoxicity assay using the SkinEthic™ reconstructed human epidermis [J].
Bernard, FX ;
Barrault, C ;
Deguercy, A ;
De Wever, B ;
Rosdy, M .
CELL BIOLOGY AND TOXICOLOGY, 2000, 16 (06) :391-400
[9]  
BOYCE S, 1990, SKIN PHARMACOL, V2, P136
[10]   DELAYED CONTACT HYPERSENSITIVITY IN GUINEA PIG [J].
BUEHLER, EV .
ARCHIVES OF DERMATOLOGY, 1965, 91 (02) :171-&