Vitamin K2 promotes the osteogenic differentiation of periodontal ligament stem cells via the Wnt/β-catenin signaling pathway

被引:12
|
作者
Cui, Qun [1 ,2 ,3 ]
Li, Na [4 ]
Nie, Fujiao [1 ,2 ,3 ]
Yang, Fan [1 ,2 ,3 ]
Li, Hongkun [1 ,2 ,3 ]
Zhang, Jun [1 ,2 ,3 ]
机构
[1] Shandong Univ, Cheeloo Coll Med, Sch & Hosp Stomatol, Dept Orthodont, 44-1 Wenhua Rd West, Jinan 250012, Shandong, Peoples R China
[2] Shandong Key Lab Oral Tissue Regenerat, 44-1 Wenhua Rd West, Jinan 250012, Shandong, Peoples R China
[3] Shandong Engn Lab Dent Mat & Oral Tissue Regenera, 44-1 Wenhua Rd West, Jinan 250012, Shandong, Peoples R China
[4] Shandong First Med Univ, Affiliated Hosp 1, Stomatol Dept, 16766 Jingshi Rd, Jinan 250012, Shandong, Peoples R China
关键词
Vitamin K2; Periodontal ligament stem cells; Proliferation; Osteogenesis; Wnt/beta-catenin signaling pathway; BONE-MINERAL DENSITY; EXPRESSION; REGENERATION; OSTEOBLASTS; OSTEOCLASTOGENESIS; PHOSPHORYLATION; CARBOXYLATION; ISOLATE; GROWTH; RUNX2;
D O I
10.1016/j.archoralbio.2021.105057
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: Vitamin K2 (MK-4, menaquinone 4) plays an important role in osteoprotection. The present study aimed to examine the effect of MK-4 on the osteogenic differentiation of periodontal ligament stem cells (PDLSCs) in vitro and probed the potential signaling pathway. Design: PDLSCs were isolated from extracted premolars by tissue block culture method and were identified by flow cytometry. Cell Counting Kit-8 (CCK-8) and colony formation assays were used to determine the effect of MK-4 on the proliferation of PDLSCs. Alkaline phosphatase (ALP) activity was analyzed quantitatively, and extracellular matrix mineralization was examined by Alizarin Red S staining. The mRNA and protein expression levels of ALP, Runx Family Transcription Factor 2 (Runx2), osteocalcin (OCN), and Sp7 Transcription Factor (SP7; Osterix) were measured by qRT-PCR and Western blot. In addition, after adding the inhibitor XAV-939, Western blot was used to assess the correlation with the Wnt/beta-catenin signaling pathway. The above results were obtained by observing at least three fields randomly, and each experiment was repeated at least three times. Results: This study found that 10 5 M MK-4 significantly promoted the osteogenic differentiation of PDLSCs. Gene and protein expression levels of ALP, Runx2, OCN, and Osterix were all upregulated compared with control. Remarkably, after blocking the Wnt/beta-catenin signaling pathway with XAV-939, the effect of MK-4 was apparently reversed. Conclusion: These results demonstrate that MK-4 can promote the osteogenic differentiation of PDLSCs, which is likely related to the activation of the Wnt/beta-catenin signaling pathway.
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页数:10
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