Isolation of Anti Ageing Molecules Secreted by Human Gingival Stem Cells. Protection of Collagen and Elastic Networks
- 1 Dental Department, A. Chenevier-H. Mondor Hospital, Créteil, France
- 2 Dental Department, A. Chenevier-H. Mondor Hospital, Créteil, France
- 3 Dental Department, A. Chenevier-H. Mondor Hospital, Créteil, France
- 4 Dental Department, A. Chenevier-H. Mondor Hospital, Creteil, France
Abstract
Skin aging results in an imbalance between synthesis and degradation of the extracellular matrix. Overproduction of degradative enzymes (MMPs) and oxygen free radicals during chronological and photo-induced aging leads a degradation of the network and elastic skin collagen. Our previous work demonstrated that a culture supernatant of gingival stem cells had anti-aging activities in vitro , ex vivo and in vivo in humans. However, this culture medium is very complex and currently not responding to the European cosmetics regulation. After the analysis of the culture medium we have isolated 4 molecules interesting in terms of skin anti-aging activity: TIMP1, Selenium, Folic Acid and Glycin (TSAG). After the study of the most efficiency concentration of each molecule, the composition of TSAG is tested on irradiated UVA human dermal fibroblast and human skin. TSAG preserves the elastin and collagen network and inhibits the MMP1, MMP3 and MMP9 activities. The advantage of this mimetic solution of stem cells is to be stable, easily reproducible and non-human origin. The outlook for cosmetology seems interesting.
- Rafferty, T.S., Green, M.H., Lowe, J.E., Arlett, C., Hunter, J.A., Beckett, G.J. and McKenzie, R.C. (2003) Effects of Selenium Compounds on Induction of DNA Damage by Broadband Ultraviolet Radiation in Human Keratinocytes. British Journal of Dermatology, 148, 1001-1009. http://dx.doi.org/10.1046/j.1365-2133.2003.05267.x
- Gogly, B., Ferré, F., Cherifi, H., Naveau, A. and Fournier, B. (2011) Inhibition of Elastin and Collagen Networks Degradation in Human Skin by Gingival Fibroblast. In Vitro, ex Vivo and in Vivo Studies. Journal of Cosmetics, Dermatological Sciences and Applications, 1, 4-14.
- Fournier, B., Ferré, F., Couty, L., Lataillade, J.J., Gourven, M., Naveau, A., Coulom, B., Lafont, A. and Gogly, B. (2010) Multipotent Progenitor Cells in Gingival Connective Tissue. Tissue Engineering Part A, 16, 2891-2899. http://dx.doi.org/10.1089/ten.tea.2009.0796
- Fournier, B., Larjava, H. and Hakkinen, L. (2013) Gingiva as a Source of Stem Cells with Therapeutic Potential. Stem Cells and Development, 22, 3157-3177. http://dx.doi.org/10.1089/scd.2013.0015
- Naveau, A., Lataillade, J.J., Fournier, B.P., Couty, L., Prat, M., Ferré, F.C., Gourven, M., Durand, E., Coulomb, B., Lafont, A. and Gogly, B. (2010) Phenotypic Study of Human Gingival Fibroblasts in a Medium Enriched with Platelet Lysate. Journal of Periodontology, 82, 632-641. http://dx.doi.org/10.1902/jop.2010.100179
- Hornebeck, W. (2003) Down-Regulation of Tissue Inhibitor of Matrix Metalloprotease-1 (TIMP-1) in Aged Human Skin Contributes to Matrix Degradation and Impaired Cell Growth and Survival. Pathologie Biologie, 51, 569-573. http://dx.doi.org/10.1016/j.patbio.2003.09.003
- Rittié, L. and Fisher, G.J. (2002) UV-Light-Induced Signal Cascades and Skin Aging. Ageing Research Reviews, 1, 705-720. http://dx.doi.org/10.1016/S1568-1637(02)00024-7
- Emonet-Piccardi, N., Richard, M.J., Ravanat, J.L., Signorini, N., Cadet, J. and Béani, J.C. (1998) Protective Effects of Antioxidants against UVA-Induced DNA Damage in Human Skin Fibroblasts in Culture. Free Radical Research, 29, 307-313. http://dx.doi.org/10.1080/10715769800300341
- McKenzie, R.C. (2000) Selenium, Ultraviolet Radiation and the Skin. Clinical and Experimental Dermatology, 25, 631-636. http://dx.doi.org/10.1046/j.1365-2230.2000.00725.x
- Stadtman, T.C. (2000) Selenium Biochemistry. Mammalian Selenoenzymes. Annals of the New York Academy of Sciences, 899, 399-402. http://dx.doi.org/10.1111/j.1749-6632.2000.tb06203.x