Naringenin stimulates osteogenic/odontogenic differentiation and migration of human dental pulp stem cells

被引:8
|
作者
Kim, Yeon [1 ,2 ,3 ]
Park, Hyun-Joo [1 ,2 ,3 ]
Kim, Mi-Kyoung [1 ,2 ]
Kim, Yong-Il [4 ]
Kim, Hyung Joon [1 ,2 ,3 ]
Bae, Soo-Kyung [2 ,3 ,5 ]
Nor, Jacques E. [6 ]
Bae, Moon-Kyoung [1 ,2 ,3 ,7 ]
机构
[1] Pusan Natl Univ, Sch Dent, Dept Oral Physiol, Yangsan, South Korea
[2] Pusan Natl Univ, Periodontal Dis Signaling Network Res Ctr MRC, Yangsan, South Korea
[3] Pusan Natl Univ, Dent & Life Sci Inst, Yangsan, South Korea
[4] Pusan Natl Univ, Sch Dent, Dept Orthodont, Yangsan, South Korea
[5] Pusan Natl Univ, Sch Dent, Dept Dent Pharmacol, Yangsan, South Korea
[6] Univ Michigan, Sch Dent, Dept Cariol, Restorat Sci,Endodont, Ann Arbor, MI USA
[7] Pusan Natl Univ, Sch Dent, Dept Oral Physiol, 49 Busandaehak ro, Yangsan 50612, South Korea
基金
新加坡国家研究基金会;
关键词
Naringenin; Human dental pulp stem cells; Differentiation; Migration; ODONTOBLASTIC DIFFERENTIATION; SIGNALING PATHWAY; OSTEOCLASTOGENESIS; PROLIFERATION;
D O I
10.1016/j.jds.2022.08.029
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background/purpose: Naringenin, a naturally occurring flavanone in citrus fruits, regulates bone formation by bone marrow-derived mesenchymal stem cells. The purpose of this study was to characterize the effects of naringenin on some biological behaviors of human dental pulp stem cells (HDPSCs).Materials and methods: HDPSCs were cultured in osteogenic differentiation medium and os-teo/odontogenic differentiation and mineralization were analyzed by alkaline phosphatase (ALP) staining and Alizarin Red S (ARS) staining. The migration of HDPSCs was evaluated by transwell chemotactic migration assays and scratch wound healing migration assay. Using tooth slice/scaffold model, we assessed the in vivo odontogenic differentiation potential of HDPSCs.Results: We have demonstrated that naringenin increases the osteogenic/odontogenic differ-entiation of HDPSCs through regulation of osteogenic-related proteins and the migratory abil-ity of HDPSCs through stromal cell derived factor-1 (SDF-1)/C-X-C chemokine receptor type 4 (CXCR4) axis. Moreover, naringenin promotes the expression of dentin matrix acidic phosphoprotein-1 (DMP-1) and dentin sialophosphoprotein (DSPP) in HDPSCs seeded on tooth slice/scaffolds that are subcutaneously implanted into immunodeficient mice.Conclusion: Our present study suggests that naringenin promotes migration and osteogenic/ odontogenic differentiation of HDPSCs and may serve as a promising candidate in dental tissue engineering and bone regeneration. 2022 Association for Dental Sciences of the Republic of China. Publishing services by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons. org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:577 / 585
页数:9
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