Developmental endothelial locus‐1 promotes osteogenic differentiation and alveolar bone regeneration in experimental periodontitis with type 2 diabetes mellitus

牙周膜干细胞 牙周炎 运行x2 牙槽 间充质干细胞 牙周纤维 医学 病理 碱性磷酸酶 牙科 生物 生物化学
作者
Qian Ma,Yiyao Hu,Han Li,Yunchun Kuang,Jie Li,Jinlin Song
出处
期刊:Journal of Periodontal Research [Wiley]
卷期号:59 (2): 355-365 被引量:3
标识
DOI:10.1111/jre.13219
摘要

Abstract Objectives This study sought to explore the role of developmental endothelial locus‐1 (DEL‐1) in osteogenic differentiation of human periodontal ligament stem cells (hPDLSCs) and investigate the therapeutic effect of DEL‐1 in ligature‐induced experimental periodontitis with type 2 diabetes mellitus (T2DM). Background T2DM is a significant risk factor for periodontitis. Treatment modalities for periodontitis with T2DM are being explored. DEL‐1 is a versatile protein that can modulate the different stages of inflammatory diseases including periodontitis. The direct effect of DEL‐1 on osteogenic differentiation of PDLSCs in periodontitis with T2DM is poorly understood. Methods Primary hPDLSCs were isolated from periodontal ligament tissue and identified by flow cytometry. In osteogenesis experiments, alkaline phosphatase (ALP), Alizarin Red staining and western blot were used to assess the osteogenic effect of DEL‐1 on hPDLSCs in high glucose and inflammation environments. The mouse model of ligature‐induced experimental periodontitis was established. H&E and Masson's trichrome staining were used to assess the change of periodontal tissue after local periodontal injection of DEL‐1. Immunohistochemical staining was used to evaluate osteogenic‐related protein expression. Results hPDLSCs expressed mesenchymal stem cell (MSC)‐specific surface markers and were negative for hematopoietic cell surface markers. hPDLSCs had the potential for multidirectional differentiation. DEL‐1 could enhance the osteogenic differentiation of hPDLSCs in high glucose and inflammation environments, although it did not return to the control level. Histological staining showed that DEL‐1 contributed to alveolar bone regeneration and osteogenic‐related protein expression, but the degree of improvement in T2DM mice was lower than in non‐T2DM mice. Conclusions In summary, we demonstrated that DEL‐1 could promote osteogenic differentiation of hPDLSCs in high glucose and inflammation environment and rescue alveolar bone loss in experimental periodontitis with T2DM, which could provide a novel therapeutic target for periodontitis with T2DM.
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