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38 TESTING In the context of dermo-cosmetic compounds


targeting the skin flora exploration, this double approach allows to investigate the potential effects on the microorganism itself, as well as the response of the tissue to this infection. Within ourMicroBIOS Platform, this interesting


twofold methodological approach is extended to the study of other living bacterial strains (Staphylococcus aureus and Staphylococcus epidermidis) and yeasts (Malassezia furfur) on RHE. Those different available in vitro 3D models and associated tests offer a promising tool to speed up the research, understanding and objectivation of innovative dermo-cosmetic actives that target the skin flora.


PC


References 1. Dagnelie MA, Corvec S, Saint-Jean M, Nguyen J-M, Khammari A ,Dréno B. Cutibacterium acnes phylotypes diversity loss: a trigger for skin inflammatory process. J Eur Acad Dermatol Venereol. 2019 Dec;33(12):2340-2348


2. Beylot C, Auffret N, Poli F, Claudel J-P, Leccia M-T, Del Giudice P, Dreno B. Propionibacterium acnes: an update on its role in the pathogenesis of acne. J Eur Acad Dermatol Venereol. 2014, 28, 271–278


3. Zheng Jun Li, Dae Kyoung Choi, Kyung Cheol Sohn, Min Seok Seo, Hae Eul Lee, Young Lee,Young Joon Seo, Young Ho Lee, Ge Shi,


Down-regulation


4.00 3.75 3.50 3.25 3.00 2.75 2.50 2.25 2.00 1.75 1.50 1.25


1.00 0.75 0.50 0.25 0.00


-1.0 -0.5 0.0 0.5 1.0 1.5 2.0 2.5 log2 (Fold Change)


Figure 4: Gene expression analysis by TaqMan Low Density Array (TLDA) technology. Volcano plot obtained by comparison of 93 gene expression in non-colonised versus Cutibacterium acnes-colonised reconstructed human epidermis, after total RNA extraction, reverse transcription and amplification using Straticell’s TLDA referred as ‘Skin Response to Microorganisms’. Y axis: statistically significant gene expression variations defined as Log10 of the p-value set at 0.05. X axis: gene expression regulation defined as the Log2 of fold change expression set at 1. Genes involved in the skin inflammation are framed in red. Genes involved in the innate immunity are framed in green. Genes involved in the skin barrier are framed in blue


PERSONAL CARE June 2022 www.personalcaremagazine.com 3.0 3.5 4.0 4.5 5.0 5.5


2000 1800 1600 1400 1200 1000 800 600 400 200 0


*** * **


CTL


CXCL-8


DEFB4


IL-1β


Figure 3: Gene expression analysis by RT-qPCR. Histogram showing the percentage of CXCL-8, IL-1β and DEFB4 gene expression in reconstructed human epidermis colonised with Cutibacterium acnes compared to non-colonised control reconstructed epidermis (CTL)


Christos C. Zouboulis, Chang Deok Kim, Jeung Hoon Lee and Myung Im. Propionibacterium acnes Activates the NLRP3 Inflammasome in Human Sebocytes. Journal of Investigative Dermatology. 2014. 134, 2747–2756


4. Leung AKC, Barankin B, Lam JM, Leong KF, Hon KL. Dermatology: how to manage acne vulgaris. Drugs in Context. 2021;10:2021-8-6


Up-regulation


5. Zaenglein AL, Pathy AL, Schlosser BJ, Alikhan A, Baldwin HE, Berson DS, Bowe WP, Graber EM, Harper JH, Sewon Kang, Keri JE, Leyden JJ, Reynolds RV, Silverberg NB, LF Stein Gold, Tollefson MM, Weiss JS, Dolan NC, Sagan AA, Stern M, Boyer KM, Bhushan R. Guidelines of care for the management of acne vulgaris. J Am Acad Dermatol. 2016;74:945-73


significanr variations Not Statistically


Statistically significant variations -log10 (P-Value)


Gene expression (% compared to control)


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