538. EXPRESSION OF STRATUM CORNEUM LIPID PATHWAYS IN HUMAN SKIN EQUIVALENT CULTURES.

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Jarrold, B., Mullins, L., Reichling, T., Tiesman, J., Robinson, M., Binder, B., Osborne, R. P&G Beauty, Cincinnati, Ohio USA. Presented at Amer. Acad. of Derm. Meeting, San Antonio (2008).

Summary:
This study by scientists at Procter & Gamble Beauty demonstrated that gene pathways involved in stratum corneum lipid formation are expressed in MatTek’s EpiDermFT full-thickness in vitro 3-D human skin tissue equivalent, suggesting that ths culture system is an appropriate in vitro approach for studying stratum corneum biology.

Human skin equivalent cultures contain living human skin cells that form a cornified stratified squamous epithelium in vitro, as determined by histological examination. It is not known the extent to which these in vitro models reproduce the lipid synthesis pathways critical to stratum corneum (SC) formation in vivo.

To examine this question, genechip analysis of two commercially available human skin equivalent cultures systems was used to determine expression of stratum corneum lipid metabolism pathways.

The goal of this work was to evaluate whether stratum corneum lipid metabolism pathways are expressed in human skin equivalent cultures, using a gene profiling approach.

The results indicate that gene pathways involved in stratum corneum lipid formation are expressed in human skin equivalent cultures, suggesting that culture systems derived from either young or older skin cells are appropriate in vitro approaches to study stratum corneum biology.

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EpiDermFT Data Sheet

EpiDermFT Specifications

EpiDermFT Technical References

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Applications: Characterization study, Genomics

Keywords: 3-hydroxy-3--methylglutaryl-Coenzyme A reductase, 3-hydroxy-3--methylglutaryl-Coenzyme A synthase 1, 7-dehydrocholesterol reductase, ATP citrate lyase, ATP-binding cassette, sub-family A, member 1, ATP-binding cassette, sub-family G, member 4, Acetyl-Coenzyme A carboxyiase alpha, Affymetrix genechips, Ceramides, Cholesterol, Cholesterol synthetic pathway, Citrate synthase, Cytochrome P450, family 51, subfamily A, polypeptide 1, Degenerative spermatocyte homolog 1, lipid desaturase, Degenerative spermatocyte homolog 2, lipid desaturase, EFT-400, EpiDerm-FT, EpiDermFT, Farnesyl diphosphate synthase, Farnesyl-diphosphate farnesyltransferase 1, Fatty acid synthase, Fatty acid synthetic pathway, Fatty acids, Follicular lymphoma variant translocation 1, Genechip analysis, Glucosidase, beta; acid, Hypothetical protein MGC26963, Isopentenyl-diphosphate delta isornerase 1, LAG1 longevity assurance homolog 2, LAG1 longevity assurance homolog 4, LAG1 longevity assurance homolog 5, LAG1 longevity assurance homolog 6, Lanosterol synthase, Lipid metabolism, Lipid synthesis, Low density lipoprotein receptor, Mevalonate decarboxylase, Mevalonate kinase, NAD(P) dependent steroid dehydrogenase-like, Oil red O staining, Phosphomevalonate kinase, Scavenger receptor class B, member 1, Serine palmitoyltransferase, long chain base subunit 1, Serine palmitoyltransferase, long chain base subunit 2, Sphingolipid processing, Sphingolipids, Sphingomyelin phosphodiesterase 1, Sphingomyelin phosphodiesterase 2, Squalene epoxidase, Sterol-C4-methyl oxidase-like, Sterol-C5-desaturase, Transmembrane protein 23, UDP-glucose ceramide glucosyltransferase

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