인문학
사회과학
자연과학
공학
의약학
농수해양학
예술체육학
복합학
지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
이용 4
초록·키워드
Dental pulp stem cells (DPSC) are a type of adult stem cells that exist in dental pulp tissue and have an immunophenotype similar to bone marrow mesenchymal stem cells (BMSC), osteoblasts, odontoblasts, muscle cells, and nerve cells. Dental pulp stem cells (DPSCs) have a higher proliferative capacity than BMSCs and have the advantage of being able to easily collect stem cells from patients compared to other tissues, so they are considered ideal in terms of tissue engineering such as tooth regeneration and nerve regeneration. Chios gum mastic (CGM) is a resin extracted from the stems and leaves of Pistacia lentiscus var Chia, a plant that grows only on the Greek island of Chios. It has been used for centuries in the Mediterranean and Middle East as a treatment for gastric and duodenal ulcers and as a food additive. Recently, attention has been paid to the effects of CGM on regenerative tissue. Our previous study demonstrated that the combined use of CGM and low-level laser therapy (LLLT) promotes the differentiation of osteoblasts through the p38 mitogen-activated protein kinase (MAPK) pathway. This study was conducted to confirm the change in cell proliferation rate and induce differentiation activity by treating hDPSC with CGM, a substance that effectively induces differentiation of osteoblasts.
In present study, hDPSCs showed low toxic sensitivity to CGM, and CGM treatment at low concentrations induced cell proliferation by activating cell-cycle proteins. In addition, it was demonstrated that CGM induces ALP activation by increasing the expression of collagen type I, a representative matrix protein of dentin, and activates odontogenic and bone differentiation markers, eventually promoting the mineralization of hDPSCs. Additional studies on dentifrice by CGM are needed, but the results of the present study suggest that the value of CGM as a new natural material that can aid in tooth regeneration can be highly evaluated.
In present study, hDPSCs showed low toxic sensitivity to CGM, and CGM treatment at low concentrations induced cell proliferation by activating cell-cycle proteins. In addition, it was demonstrated that CGM induces ALP activation by increasing the expression of collagen type I, a representative matrix protein of dentin, and activates odontogenic and bone differentiation markers, eventually promoting the mineralization of hDPSCs. Additional studies on dentifrice by CGM are needed, but the results of the present study suggest that the value of CGM as a new natural material that can aid in tooth regeneration can be highly evaluated.
목차
- 1. Introduction 12. Materials and Methods 32.1. Cell culture 32.2. MTT assay 32.3. Proliferation assay 32.4. Cell Cycle Analysis Using Flow Cytometry 42.5. Immunofluorescence Staining 42.6. Western blot assay 52.7. RNA Isolation and RT-qPCR 62.8. Alizarin Red Staining 72.9. Alkaline Phosphatase (ALP) Activity 72.10. Statistical analysis 83. Results 93.1. CGM Treatment Induces Cell Proliferation Without Cytotoxicity in hDPSCs. 93.2. CGM Treatment Promotes Activation of Cell Proliferation by Ki-67 and the S Phase of the Cell Cycle in hDPSCs 93.3. CGM Increases the Mineralization and Odontogenic Differentiation of hDPSCs 104. Discussion 215. References 246. Korean abstract 27