Ujjal K Bhawal1, Xiaoyan Li2,3, Masatoshi Suzuki2, Chieko Taguchi4, Shunichi Oka2, Kazumune Arikawa4, Nitesh Tewari5, Yi Liu3. 1. Department of Biochemistry and Molecular Biology, Nihon University School of Dentistry at Matsudo, Chiba, Japan. 2. Department of Anesthesiology, Nihon University School of Dentistry at Matsudo, Chiba, Japan. 3. Laboratory of Tissue Regeneration and Immunology and Department of Periodontics, Beijing Key Laboratory of Tooth Regeneration and Function Reconstruction, School of Stomatology, Capital Medical University, Beijing, China. 4. Department of Community Oral Health, Nihon University School of Dentistry at Matsudo, Chiba, Japan. 5. Division of Pedodontics and Preventive Dentistry, Centre for Dental Education and Research, All India Institute of Medical Sciences, New Delhi, India.
Abstract
BACKGROUND/AIMS: Lacerations of the oral mucosa and fractures of alveolar processes commonly occur in traumatic dental injuries (TDIs). Impaired wound healing and tissue regeneration have severe consequences on the quality of life. Bone marrow mesenchymal stem cells (BMMSCs) possess the ability of self-renewal and multipotential differentiation. Treatment with low-level sodium fluoride (NaF) has emerged as a promising approach to enhance wound repair. The aim of this study was to assess the effects of low-level NaF on soft tissue healing and on the proliferation, migration and extracellular matrix synthesis of BMMSCs. MATERIAL AND METHODS: BMMSCs derived from mice were treated with 50 μM, 500 μM, or 5 mM NaF for 12, 24, and 48 hours, and cell proliferation was assessed by the MTS assay. Cell motility was detected at 12 and 24 hours by a wound healing assay, and osteoblastic differentiation for 21 days by 1% Alizarin Red S staining in 50 μM NaF-treated BMMSCs. Gene expression of Runx2 and Osteocalcin was evaluated by quantitative real-time PCR. An experimental rat skin wound model was employed, and levels of c-Myc, Ki67, fibronectin, and vimentin were assessed by immunohistochemistry. RESULTS: There was a significant induction in the proliferation and migration of BMMSCs treated with 50 μM NaF. The expression of Ki67 and c-Myc protein was increased in tissues treated with 50 μM NaF, and the expression of fibronectin and vimentin in the 50 μM NaF-treated tissues was stimulated. Alizarin Red staining revealed enhanced mineralization in 50 μM NaF-treated BMMSCs with increased expression of Runx2 and Osteocalcin, indicating their upregulated osteogenic differentiation. CONCLUSION: Low-level NaF could promote soft tissue healing and hard tissue regeneration.
BACKGROUND/AIMS: Lacerations of the oral mucosa and fractures of alveolar processes commonly occur in traumatic dental injuries (TDIs). Impaired wound healing and tissue regeneration have severe consequences on the quality of life. Bone marrow mesenchymal stem cells (BMMSCs) possess the ability of self-renewal and multipotential differentiation. Treatment with low-level sodium fluoride (NaF) has emerged as a promising approach to enhance wound repair. The aim of this study was to assess the effects of low-level NaF on soft tissue healing and on the proliferation, migration and extracellular matrix synthesis of BMMSCs. MATERIAL AND METHODS: BMMSCs derived from mice were treated with 50 μM, 500 μM, or 5 mM NaF for 12, 24, and 48 hours, and cell proliferation was assessed by the MTS assay. Cell motility was detected at 12 and 24 hours by a wound healing assay, and osteoblastic differentiation for 21 days by 1% Alizarin Red S staining in 50 μM NaF-treated BMMSCs. Gene expression of Runx2 and Osteocalcin was evaluated by quantitative real-time PCR. An experimental rat skin wound model was employed, and levels of c-Myc, Ki67, fibronectin, and vimentin were assessed by immunohistochemistry. RESULTS: There was a significant induction in the proliferation and migration of BMMSCs treated with 50 μM NaF. The expression of Ki67 and c-Myc protein was increased in tissues treated with 50 μM NaF, and the expression of fibronectin and vimentin in the 50 μM NaF-treated tissues was stimulated. Alizarin Red staining revealed enhanced mineralization in 50 μM NaF-treated BMMSCs with increased expression of Runx2 and Osteocalcin, indicating their upregulated osteogenic differentiation. CONCLUSION: Low-level NaF could promote soft tissue healing and hard tissue regeneration.
Authors: Abu Shufian Ishtiaq Ahmed; Matilda H C Sheng; Kin-Hing William Lau; Sean M Wilson; M Daniel Wongworawat; Xiaolei Tang; Mahdis Ghahramanpouri; Antoine Nehme; Yi Xu; Amir Abdipour; Xiao-Bing Zhang; Samiksha Wasnik; David J Baylink Journal: Am J Physiol Cell Physiol Date: 2022-04-06 Impact factor: 5.282