4.5 Article

Expression profiles of phases 1 and 2 metabolizing enzymes in human skin and the reconstructed skin models Episkin™ and full thickness model from Episkin™

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jsbmb.2009.05.011

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Episkin; Phase 1 enzymes; Phase 2 enzymes; Cytochrome P450; Metabolizing enzymes; Human skin; Reconstructed skin; Expression profile

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Background: Episkin (TM) and full thickness model from Episkin (TM) (FTM) are human skin models obtained from in vitro growth of keratinocytes into the five typical layers of the epidermis. FTM is a full thickness reconstructed skin model that also contains fibroblasts seeded in a collagen matrix. Objectives: To assess whether enzymes involved in chemical detoxification are expressed in Episkin (TM) and FTM and how their levels compare with the human epidermis, dermis and total skin. Methods: Quantification of the mRNA expression levels of phases 1 and 2 metabolizing enzymes in cultured Episkin (TM) and FTM and human epidermis, dermis and total skin using Realtime PCR. Results: The data show that the expression profiles of 61 phases 1 and 2 metabolizing enzymes in Episkin (TM), FTM and epidermis are generally similar, with some exceptions. Cytochrome P450-dependent enzymes and flavin monooxygenases are expressed at low levels, while phase 2 metabolizing enzymes are expressed at much higher levels, especially, glutathione-S-transferase P1 (GSTP1) catechol-O-methyl transferase (COMT), steroid sulfotransferase (SULT2B1b), and N-acetyl transferase (NAT5). The present study also identifies the presence of many enzymes involved in cholesterol, arachidonic acid, leukotriene, prostaglandin, eicosatrienoic acids, and vitamin D3 metabolisms. Conclusion: The present data strongly suggest that Episkin (TM) and FTM represent reliable and valuable in vitro human skin models for studying the function of phases 1 and 2 metabolizing enzymes in xenobiotic metabolisms. They could be used to replace invasive methods or laboratory animals for skin experiments. (C) 2009 Elsevier Ltd. All rights reserved.

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