1. Effect of nano zinc oxide on proliferation and toxicity of human gingival cells.
- Author
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Chen, Fang-Chuan, Huang, Cong-Ming, Yu, Xiao-Wan, and Chen, Ya-Yu
- Subjects
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OPERATIVE dentistry , *FLOW cytometry , *BIOLOGICAL models , *FIBROBLASTS , *STAINS & staining (Microscopy) , *ZINC oxide , *IMMUNOHISTOCHEMISTRY , *WESTERN immunoblotting , *POSTOPERATIVE care , *APOPTOSIS , *GENE expression , *CELL proliferation , *SURGICAL site , *TOXICITY testing , *RESEARCH funding , *BIOLOGICAL assay , *POLYMERASE chain reaction , *GINGIVA , *NANOPARTICLES , *DRUG toxicity , *PERIODONTICS , *SURGICAL dressings , *BANDAGES & bandaging - Abstract
Background: Periodontal dressing is used to cover the gum surface and protect the wound after periodontal surgery. Nanomaterials have been widely applied in dentistry in recent years. Zinc oxide (ZnO) is one of the main components of periodontal dressing. Aim: This study aims to explore the toxicity ZnO nanoparticles (ZnO NPs) causes to human gingival fibroblast cells (HGF-1) and its effect on cell proliferation. Methods: First, we identified and analyzed HGF-1, including cell morphology, growth curve, and immunohistochemistry staining. Then, we treated HGF-1 with ZnO NP. Cell viability, the integrity of the cell membrane, oxidative damage, and apoptosis were measured by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, lactate dehydrogenase (LDH) release assay, fluorescent probe, and flow cytometry. Furthermore, the expression of murine double minute 2 (MDM2) and p53 was determined by quantitative real-time polymerase chain reaction (qPCR) and Western blotting. We finally overexpressed MDM2 in HGF-1 to verify the relationship between MDM2 and cell proliferation. Results: Our research indicated ZnO NPs did not affect cell proliferation at low concentrations. However, high-concentration ZnO NP inhibited cell proliferation, destroyed the integrity of cell membranes, and induced oxidative stress and apoptosis. In addition, high concentration of ZnO NPs inhibited the proliferation of HGF-1 by regulating the expression of MDM2 and p53. Conclusion: High concentration of ZnO NP caused toxicity to HGF-1 cells and inhibited cell proliferation by regulating MDM2 and p53 expression. [ABSTRACT FROM AUTHOR]
- Published
- 2022
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