LS8 cell apoptosis induced by NaF through p-ERK and p-JNK – a mechanism study of dental fluorosis

Authors

  • Lin Zhao Clinical Research Center of Shaanxi Province for Dental and Maxillofacial Diseases, Department of Preventive Dentistry, Stomatology Hospital, Xi'an Jiaotong University, Xi’an, PR China; Department of Oral Pathology, Stomatology Hospital, Ningxia Medical University, Yinchuan, PR China
  • Juedan Li Clinical Research Center of Shaanxi Province for Dental and Maxillofacial Diseases, Department of Preventive Dentistry, Stomatology Hospital, Xi'an Jiaotong University, Xi’an, PR China
  • Jiali Su Clinical Research Center of Shaanxi Province for Dental and Maxillofacial Diseases, Department of Preventive Dentistry, Stomatology Hospital, Xi'an Jiaotong University, Xi’an, PR China; Department of Endodontics, Yinchuan Stomatology Hospital, Yinchuan, PR China
  • Malcolm L. Snead Herman Ostrow School of Dentistry of USC, Center for Craniofacial Molecular Biology, University of Southern California, Los Angeles, CA, USA
  • Jianping Ruan Clinical Research Center of Shaanxi Province for Dental and Maxillofacial Diseases, Department of Preventive Dentistry, Stomatology Hospital, Xi'an Jiaotong University, Xi’an, PR China

DOI:

https://doi.org/10.1080/00016357.2016.1214980

Keywords:

NaF, LS8, apoptosis, mitogen-activated protein kinase, dental fluorosis

Abstract

Objective: To investigate the possible biological mechanism of dental fluorosis at a molecular level.

Material and methods: Cultured LS8 were incubated with serum-free medium containing selected concentrations of NaF (0 ∼ 2 mM) for either 24 or 48 h. Subcellular microanatomy was characterized using TEM; meanwhile, selected biomolecules were analysed using various biochemistry techniques. Transient transfection was used to modulate a molecular pathway for apoptosis.

Results: Apoptosis of LS8 was induced by NaF treatment that showed both time and concentration dependency. The activity of caspase-3, -8, -9 was found to be increased with NaF in a dose-dependent manner. Western blot revealed that the protein expression of p-ERK and p-JNK were decreased, while the expression of p-P38 was increased. Inhibition of the p-ERK and p-JNK pathways resulted in a similar decrease for caspase-3.

Conclusion: During NaF-induced apoptosis of LS8, p-ERK and p-JNK were closely associated with induction of apoptosis, which might be a mechanism of dental fluorosis.

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Published

2016-10-02