Chios gum mastic enhance the proliferation and odontogenic differentiation of human dental pulp stem cells

被引:0
|
作者
Baek, Hyun-Su [1 ]
Park, Se-Jin [1 ]
Lee, Eun-Gyung [2 ,4 ]
Kim, Yong-Il [3 ,4 ]
Kim, In-Ryoung [1 ,4 ]
机构
[1] Pusan Natl Univ, Sch Dent, Dept Oral Anat, Yangsan 50612, South Korea
[2] Pusan Natl Univ, Sch Dent, Dept Pediat Dent, Yangsan 50612, South Korea
[3] Pusan Natl Univ, Sch Dent, Dept Orthodont, Yangsan 50612, South Korea
[4] Pusan Natl Univ, Dent & Life Sci Inst, Sch Dent, Yangsan 50612, South Korea
来源
KOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY | 2024年 / 28卷 / 05期
基金
新加坡国家研究基金会;
关键词
Cell proliferation; Chios gum mastic; Dental pulp stem cells; Odontogenic differentiation; CATENIN; TISSUE; CENTROSOME; MATRIX;
D O I
10.4196/kjpp.2024.28.5.423
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Dental pulp stem cells (DPSCs) are a type of adult stem cell present in the dental pulp tissue. They possess a higher proliferative capacity than bone marrow mesenchymal stem cells. Their ease of collection from patients makes them well-suited for tissue engineering applications, such as tooth and nerve regeneration. Chios gum mastic (CGM), a resin extracted from the stems and leaves of Pistacia lentiscus var. Chia, has garnered attention for its potential in tissue regeneration. This study aims to confirm alterations in cell proliferation rates and induce differentiation in human DPSCs (hDPSCs) through CGM treatment, a substance known for effectively promoting odontogenic differentiation. Administration of CGM to hDPSC cells was followed by an assessment of cell survival, proliferation, and odontogenic differentiation through protein and gene analysis. The study revealed that hDPSCs exhibited low sensitivity to CGM toxicity. CGM treatment induced cell proliferation by activating cell-cycle proteins through the Wnt/beta-catenin pathway. Additionally, the study demonstrated that CGM enhances alkaline phosphatase activation by upregulating the expression of collagen type I, a representative matrix protein of dentin. This activation of markers associated with odontogenic and bone differentiation ultimately facilitated the mineralization of hDPSCs. This study concludes that CGM, as a natural substance, fosters the cell cycle and cell proliferation in hDPSCs. Furthermore, it triggers the transcription of odontogenic and osteogenic markers, thereby facilitating odontogenic differentiation.
引用
收藏
页码:423 / 433
页数:11
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