Stratum Corneum. Epidermis. Dermis. Viable Fibroblasts. 4c. 3 Days. 6 Days. 10 Days. 13 Days. Evaluation of Cosmetic Ingredients in Tissue Engineered Human Skin In Vitro. Rosemarie Osborne, Ph.D., Lisa A. Mullins, B.S., Bradley B. Jarrold, M.S., Sara McPhail, B.S., Larry Robinson, Ph.D.
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Evaluation of Cosmetic Ingredients in Tissue Engineered Human Skin In Vitro
Rosemarie Osborne, Ph.D., Lisa A. Mullins, B.S., Bradley B. Jarrold, M.S., Sara McPhail, B.S., Larry Robinson, Ph.D.
The Procter & Gamble Company, Cincinnati, Ohio USA
As part of our ongoing search for predictive tools to understand skin responses, we are evaluating tissue engineered human skin equivalent cultures. Of particular interest is understanding of skin cell responses to compounds, such as N-acetyl glucosamine and niacinamide, that are included in cosmetic skin care compositions. Such compositions include those intended for use by individuals with signs of facial skin aging.
Stimulation of Hyaluronan and Collagen Expression with N-Acetyl Glucosamine and Niacinamide in Full-Thickness Epidermal-Dermal Skin Equivalent Cultures
Full thickness skin equivalent cultures contain a cornified stratified squamous epithelium and a fibroblast-containing dermis (Fig. 1). Following a 24-hr topical treatment with N-acetyl glucosamine, hyaluronan (Fig. 2a) and procollagen-1 (Fig. 2b) increased significantly relative to vehicle control, and in a dose-responsive manner. In addition, the combination of low concentrations of N-acetyl glucosamine and niacinamide acted synergistically to increase procollagen-1 (Fig. 3).
Decreased Melanin with N-Acetyl Glucosamine and Niacinamide in Melanocyte-containing Epidermal Cultures
The cultures evaluated contain a cornified stratified squamous epithelium and melanin producing melanocytes (Fig. 4). A top view reveals stellate melanocytes together with cuboidal keratinocytes (Fig. 4a). In cross-section, the melanocytes are located on the basement membrane and transfer melanin to the differentiating keratinocytes (Fig. 4b, paraffin sections with Fontana-Masson stain). The cultures pigment over a 13 day growth period (Fig. 4c, cultures are 1 cm in diameter). Individual treatments with niacinamide and N-acetyl glucosamine decreased melanin formation, and acted synergistically to reduce melanin (Fig. 5).
Figure 1. Human Full-Thickness Skin Cultures
Figure 3. Synergy between N-Acetyl Glucosamine and Niacinamide to Increase Procollagen-1
To define in vitro responses of epidermal-dermal and melanocyte-containing human skin equivalent cultures to compounds used in anti-aging cosmetic products.
*p < 0.01 vs control; t-test.
Figure 2. Increased Hyaluronan (a) and Procollagen-1 (b) with N-Acetyl Glucosamine
Figure 4. Human Melanocyte-Epidermal Cultures
In Vitro Human Skin Equivalents
The MatTek Human Skin EpiDermFT and Melanoderm Skin Models (MatTek Corp.) were treated with solutions of test compounds (100 ul/culture) applied topically to the stratum corneum surface of the skin equivalent cultures for 1 to 7 days at 37°C.
Hyaluronan and Procollagen 1 in cell extracts were measured by ELISA (Corgenix; Takara Bio Inc.), and normalized to total protein (Coomassie blue). mRNA levels were measured by RT-PCR (Qiagen Inc.). Melanin was measured spectrophotometrically (450 nm, VMax, Molecular Devices Corp.), and compared to a standard curve of synthetic melanin (Sigma Chemicals) for quantification. Mean biomarker values from n=4 cultures and representative of at least 3 independent experiments are shown; SEM values were <10% of mean.
Figure 5. Deceased Melanin Production with
N-Acetyl Glucosamine and Niacinamide
*p < 0.05 vs control; t-test.
*p < 0.01 vs control; t-test.
This work was funded
by P&G Beauty