Effects of retinoic acid on keratinocyte proliferation and differentiation in a psoriatic skin model
- PMID: 21417679
- DOI: 10.1089/ten.TEA.2010.0463
Effects of retinoic acid on keratinocyte proliferation and differentiation in a psoriatic skin model
Abstract
Psoriasis is a skin disease characterized by the presence of red plaques on the skin. This pathology is well-known to be a retinoid-sensitive disease. Previous investigations have shown that retinoids can modulate epidermal proliferation with an antiproliferative potential in hyperproliferative skins. The aim of this study was to compare the development of psoriatic substitutes cultured in a retinoic acid supplemented medium with those cultured in medium receiving no supplement, to define the effects of this growth factor on keratinocyte proliferation and differentiation. The self-assembly method was used to create substitutes. Characterization of the psoriatic substitutes was performed by histological and immunolabeling analyses. Results showed that psoriatic keratinocyte substitutes cultured with retinoic acid have a thinner epidermis compared with psoriatic keratinocyte substitutes cultured without this supplement. Further, the expression of all tested cell differentiation markers was restored in psoriatic keratinocyte substitutes cultured in presence of retinoic acid. No significant change in epidermal thickness or in the expression of late differentiation markers was observed in healthy keratinocyte substitutes cultured with or without retinoic acid; however, some changes were reported for proliferation and early differentiation markers. Results suggest that retinoic acid can modulate epidermal differentiation and proliferation with an antiproliferative potential in psoriatic substitutes such as observed in psoriatic skin in vivo.
Similar articles
-
Negative regulation of two hyperproliferative keratinocyte differentiation markers by a retinoic acid receptor-specific retinoid: insight into the mechanism of retinoid action in psoriasis.Cell Growth Differ. 1996 Dec;7(12):1783-91. Cell Growth Differ. 1996. PMID: 8959347
-
Development of an in vitro psoriatic skin model by tissue engineering.J Dermatol Sci. 2009 Jan;53(1):19-25. doi: 10.1016/j.jdermsci.2008.07.009. Epub 2008 Sep 9. J Dermatol Sci. 2009. PMID: 18783923
-
All-trans-retinoic acid and 13-cis-retinoic acid: pharmacokinetics and biological activity in different cell culture models of human keratinocytes.Horm Metab Res. 2007 Feb;39(2):136-40. doi: 10.1055/s-2007-961813. Horm Metab Res. 2007. PMID: 17326009
-
Epidermal effects of retinoids: in vitro studies.J Am Acad Dermatol. 1986 Oct;15(4 Pt 2):789-97. doi: 10.1016/s0190-9622(86)70235-1. J Am Acad Dermatol. 1986. PMID: 2429999 Review.
-
Experimental models for psoriasis.J Invest Dermatol. 1990 Nov;95(5 Suppl):56S-58S. doi: 10.1111/1523-1747.ep12505791. J Invest Dermatol. 1990. PMID: 16788635 Review.
Cited by
-
Successful Treatment of Nail Lichen Planus with a Lacquer Containing Urea, Keratinase, and a Retinoid Molecule: Report of 10 Cases.Case Rep Dermatol. 2022 Mar 21;14(1):43-48. doi: 10.1159/000523796. eCollection 2022 Jan-Apr. Case Rep Dermatol. 2022. PMID: 35496502 Free PMC article.
-
Antipsoriatic Potential of Quebecol and Its Derivatives.Pharmaceutics. 2022 May 26;14(6):1129. doi: 10.3390/pharmaceutics14061129. Pharmaceutics. 2022. PMID: 35745702 Free PMC article.
-
A 3D-psoriatic skin model for dermatological testing: The impact of culture conditions.Biochem Biophys Rep. 2016 Sep 30;8:268-276. doi: 10.1016/j.bbrep.2016.09.012. eCollection 2016 Dec. Biochem Biophys Rep. 2016. PMID: 28955966 Free PMC article.
-
Activating a Reserve Neural Stem Cell Population In Vitro Enables Engraftment and Multipotency after Transplantation.Stem Cell Reports. 2019 Apr 9;12(4):680-695. doi: 10.1016/j.stemcr.2019.02.014. Epub 2019 Mar 28. Stem Cell Reports. 2019. PMID: 30930245 Free PMC article.
-
Epidermal Delivery of Retinyl Palmitate Loaded Transfersomes: Penetration and Biodistribution Studies.Pharmaceutics. 2020 Jan 30;12(2):112. doi: 10.3390/pharmaceutics12020112. Pharmaceutics. 2020. PMID: 32019144 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical