Abstract
Silver-based products have been proven to be effective in retarding and preventing bacterial growth since ancient times. In the field of restorative dentistry, the use of silver ions/nanoparticles has been explored to counteract bacterial infections, as silver can destroy bacterial cell walls by reacting with membrane proteins. However, it is also cytotoxic towards eukaryotic cells, which are capable of internalizing nanoparticles. In this work, we investigated the biological effects of Chitlac-nAg, a colloidal system based on a modified chitosan (Chitlac), administered for 24–48 h to a co-culture of primary human gingival fibroblasts and Streptococcus mitis in the presence of saliva, developed to mimic the microenvironment of the oral cavity. We sought to determine its efficiency to combat oral hygiene-related diseases without affecting eukaryotic cells. Cytotoxicity, reactive oxygen species production, apoptosis induction, nanoparticles uptake, and lysosome and autophagosome metabolism were evaluated. In vitro results show that Chitlac-nAg does not exert cytotoxic effects on human gingival fibroblasts, which seem to survive through a homoeostasis mechanism involving autophagy. That suggests that the novel biomaterial Chitlac-nAg could be a promising tool in the field of dentistry.
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Acknowledgments
This work was supported by a two sources: first, a FIRB project, “Accordi di programma 2010”, directed by Prof. Cataldi (Cod.RBAPI095), on “Processi degenerativi dei tessuti mineralizzati del cavo orale, impieghi di biomateriali e controllo delle interazioni con microrganismi dell’ambiente”; and second, an “ex 60 %” grant held by Dr. di Giacomo. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The authors would like to thank Sheila Beatty for editing the English usage of the manuscript.
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Gallorini, M., di Giacomo, V., Di Valerio, V. et al. Cell-protection mechanism through autophagy in HGFs/S. mitis co-culture treated with Chitlac-nAg. J Mater Sci: Mater Med 27, 186 (2016). https://doi.org/10.1007/s10856-016-5803-5
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DOI: https://doi.org/10.1007/s10856-016-5803-5