PMID- 22854010 OWN - NLM STAT- MEDLINE DCOM- 20130506 LR - 20171116 IS - 1952-4013 (Electronic) IS - 1167-1122 (Linking) VI - 22 IP - 5 DP - 2012 Sep-Oct TI - Human beta-defensin-2 and psoriasin, two new innate immunity targets of zinc gluconate. PG - 634-9 LID - 10.1684/ejd.2012.1800 [doi] AB - BACKGROUND: Antimicrobial peptides (AMPs) are a large family of peptides implicated in innate immunity, especially in the epidermis. Zinc gluconate has been proven to be efficient to treat inflammatory dermatoses, such as acne vulgaris. OBJECTIVES: The aim of our work was to determine whether AMPs could be new targets of zinc gluconate treatment in inflammatory dermatoses. MATERIAL AND METHODS: To test this hypothesis, we used an ex vivo lipopolysaccharide (LPS)-induced inflammatory skin explant model, with or without zinc gluconate pretreatment. We evaluated human beta-defensin-2 (hBD-2), human beta-defensin-4 (hBD-4) and psoriasin protein expression and release by immunohistochemistry and ELISA, as well as the mRNA expression level by quantitative PCR. RESULTS: We found that hBD-2 and psoriasin mRNA expression levels and hBD-2 extracellular release, but not hBD-4 expression and release, were significantly upregulated by zinc gluconate in LPS-stimulated inflammatory skin explants. CONCLUSION: These results suggest that hBD-2 and psoriasin may be two main targets of zinc gluconate, involved in its anti-inflammatory activity in dermatoses. FAU - Poiraud, Carole AU - Poiraud C AD - Inserm U892, Department of Dermato-Oncology Nantes University Hospital, 1 Place Alexis-Ricordeau, 44093 Nantes, France. FAU - Quereux, Gaelle AU - Quereux G FAU - Knol, Anne-Chantal AU - Knol AC FAU - Zuliani, Thomas AU - Zuliani T FAU - Allix, Remy AU - Allix R FAU - Khammari, Amir AU - Khammari A FAU - Dreno, Brigitte AU - Dreno B LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - France TA - Eur J Dermatol JT - European journal of dermatology : EJD JID - 9206420 RN - 0 (DEFB4A protein, human) RN - 0 (Gluconates) RN - 0 (Lipopolysaccharides) RN - 0 (RNA, Messenger) RN - 0 (S100 Calcium Binding Protein A7) RN - 0 (S100 Proteins) RN - 0 (S100A7 protein, human) RN - 0 (beta-Defensins) RN - R4R8J0Q44B (gluconic acid) SB - IM MH - Gene Expression/drug effects MH - Gluconates/*pharmacology MH - Humans MH - In Vitro Techniques MH - Lipopolysaccharides/pharmacology MH - RNA, Messenger/metabolism MH - S100 Calcium Binding Protein A7 MH - S100 Proteins/genetics/*metabolism MH - Skin/drug effects/*metabolism MH - Statistics, Nonparametric MH - Up-Regulation/*drug effects MH - beta-Defensins/genetics/*metabolism EDAT- 2012/08/03 06:00 MHDA- 2013/05/07 06:00 CRDT- 2012/08/03 06:00 PHST- 2012/08/03 06:00 [entrez] PHST- 2012/08/03 06:00 [pubmed] PHST- 2013/05/07 06:00 [medline] AID - ejd.2012.1800 [pii] AID - 10.1684/ejd.2012.1800 [doi] PST - ppublish SO - Eur J Dermatol. 2012 Sep-Oct;22(5):634-9. doi: 10.1684/ejd.2012.1800.