http://www.cnr.it/ontology/cnr/individuo/prodotto/ID27622
Influence of a commercial tattoo ink on protein production in human fibroblasts. (Articolo in rivista)
- Type
- Label
- Influence of a commercial tattoo ink on protein production in human fibroblasts. (Articolo in rivista) (literal)
- Anno
- 2009-01-01T00:00:00+01:00 (literal)
- Alternative label
Falconi M, Teti G, Zago M, Galanzi A, Breschi L, Pelotti S, Ruggeri A, Mazzotti G. (2009)
Influence of a commercial tattoo ink on protein production in human fibroblasts.
in Archives of dermatological research (Print)
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- Falconi M, Teti G, Zago M, Galanzi A, Breschi L, Pelotti S, Ruggeri A, Mazzotti G. (literal)
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- Department of Anatomical Sciences, University of Bologna, via Irnerio, 48, 40126 Bologna, Italy; Polo ScientiWco-Didattico di Rimini, University of Bologna, 40100 Bologna, Italy; Unit of Dental Sciences and Biomaterials, Department of Biomedicine, University of Trieste, 34138 Trieste, Italy; Unit of Bologna c/o IOR, IGM-CNR, Bologna, Italy; Section of Legal Medicine, Department of Medicine and Public Health, University of Bologna, 40126 Bologna, Italy. (literal)
- Titolo
- Influence of a commercial tattoo ink on protein production in human fibroblasts. (literal)
- Abstract
- Tattooing is an ancient art and is still widely practiced all over the world. Since the biocompatibility of tattoo dyes has not been well researched, we studied the toxicity of a commercial tattoo ink, commonly used in tattoo lab and esthetic centers, on human fibroblasts. To test cell viability, MTT assays were carried out and scanning electron microscopy to visualize changes in the cell surface after the dye exposure was performed. A possible influence of the pigment on the expression of procollagen alpha1 type I protein was visualized by western blotting analysis. The results showed a reduction in cell viability, and electron microscopy demonstrated an unmodified cell surface completely covered by pigment particles. Western blotting analysis demonstrated a clear interference of the pigment on the expression of procollagen alpha1 type I protein. These data demonstrated that the commercial tattoo dye has a time-dependent effect on protein expression. A possible connection of the influence of the tattoo ink with clinical effects is discussed. (literal)
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