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The Effect of Vitamin D3 and Silver Nanoparticles on HaCaT Cell Viability
Authors:Samuela Cataldi  Maria Rachele Ceccarini  Federica Patria  Tommaso Beccari  Martina Mandarano  Ivana Ferri  Andrea Lazzarini  Francesco Curcio  Elisabetta Albi
Affiliation:1.Department of Pharmaceutical Sciences, University of Perugia, 06126 Perugia, Italy; (S.C.); (M.R.C.); (F.P.); (T.B.);2.Division of Pathological Anatomy and Histology, Department of Experimental Medicine, School of Medicine and Surgery, University of Perugia, 06126 Perugia, Italy; (M.M.); (I.F.);3.Crabion S.R.L., 06100 Perugia, Italy;4.Institute of Clinical Pathology, Department of Medicine, University of Udine, 33100 Udine, Italy;
Abstract:Vitamin D3, known to regulate bone homeostasis, has recently been shown to have many pleiotropic effects in different tissues and organs due to the presence of its receptor in a wide range of cells. Our previous study demonstrated that vitamin D3 was able to increase the wound healing respect to the control sample, 24 h after cutting, without however leading to a complete repair. The aim of the study was to combine vitamin D3 with silver nanoparticles to possibly enable a faster reparative effect. The results showed that this association was capable of inducing a complete wound healing only after 18 h. Moreover, a treatment of vitamin D3 + silver nanoparticles yielded a small percentage of keratinocytes vimentin-positive, suggesting the possibility that the treatment was responsible for epithelial to mesenchymal transition of the cells, facilitating wound healing repair. Since vitamin D3 acts via sphingolipid metabolism, we studied the expression of gene encoding for the metabolic enzymes and protein level. We found an increase in neutral sphingomyelinase without involvement of neutral ceramidase or sphingosine kinase2. In support, an increase in ceramide level was identified by Ultrafast Liquid Chromatography–Tandem Mass Spectrometry, suggesting a possible involvement of ceramides in wound healing process.
Keywords:wound healing   cholecalciferol   silver nanoparticles   sphingomyelinase   keratinocytes
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