WDR36 inhibits the osteogenic differentiation and migration of periodontal ligament stem cells.

IF 3.6 3区 医学 Q3 CELL & TISSUE ENGINEERING
Yi Wang, Feng-Qiu Zhang, Zhi-Peng Fan, Xin-Ling Zhu, Wan-Hao Yan, Xiu-Li Zhang
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引用次数: 0

Abstract

Background: Periodontitis is an inflammatory disease caused by the host's immune response and various interactions between pathogens, which lead to the loss of connective tissue and bone. In recent years, mesenchymal stem cell (SC) transplantation technology has become a research hotspot, which can form periodontal ligament, cementum, and alveolar bone through proliferation and differentiation.

Aim: To elucidate the regulatory effects of WD repeat-containing protein 36 (WDR36) on the senescence, migration, and osteogenic differentiation of periodontal ligament SCs (PDLSCs).

Methods: The migration and chemotaxis of PDLSCs were detected by the scratch-wound migration test and transwell chemotaxis test. Alkaline phosphatase (ALP) activity, Alizarin red staining, calcium content, and real-time reverse transcription polymerase chain reaction (RT-qPCR) of key transcription factors were used to detect the osteogenic differentiation function of PDLSCs. Cell senescence was determined by senescence-associated β-galactosidase staining.

Results: The 24-hour and 48-hour scratch-wound migration test and 48-hour transwell chemotaxis test showed that overexpression of WDR36 inhibited the migration/chemotaxis of PDLSCs. Simultaneously, WDR36 depletion promoted the migration/chemotaxis of PDLSCs. The results of ALP activity, Alizarin red staining, calcium content, and RT-qPCR showed that overexpression of WDR36 inhibited the osteogenic differentiation of PDLSCs, and WDR36 depletion promoted the osteogenic differentiation of PDLSCs. Senescence-associated β-galactosidase staining showed that 0.1 μg/mL icariin (ICA) and overexpression of WDR36 inhibited the senescence of PDLSCs, and WDR36 depletion promoted the osteogenic differentiation of PDLSCs.

Conclusion: WDR36 inhibits the migration and chemotaxis, osteogenic differentiation, and senescence of PDLSCs; 0.1 μg/mL ICA inhibits the senescence of PDLSCs. Therefore, WDR36 might serve as a target for periodontal tissue regeneration and the treatment of periodontitis.

WDR36抑制牙周韧带干细胞成骨分化和迁移。
背景:牙周炎是由宿主的免疫反应和病原体之间的各种相互作用引起的炎症性疾病,导致结缔组织和骨骼的损失。间充质干细胞(mesenchymal stem cell, SC)通过增殖分化形成牙周韧带、牙骨质和牙槽骨,近年来成为研究热点。目的:探讨WDR36 (WD repeat-containing protein 36, WDR36)对牙周韧带SCs (periodontal ligament SCs, PDLSCs)衰老、迁移和成骨分化的调控作用。方法:采用划痕迁移试验和跨井趋化试验检测PDLSCs的迁移和趋化性。采用碱性磷酸酶(ALP)活性、茜素红染色、钙含量、关键转录因子实时逆转录聚合酶链反应(RT-qPCR)检测PDLSCs的成骨分化功能。衰老相关β-半乳糖苷酶染色测定细胞衰老程度。结果:24小时、48小时划痕迁移实验和48小时transwell趋化实验显示,过表达WDR36抑制PDLSCs的迁移/趋化。同时,WDR36缺失促进了PDLSCs的迁移/趋化性。ALP活性、茜素红染色、钙含量、RT-qPCR结果显示,WDR36过表达抑制了PDLSCs的成骨分化,而WDR36缺失促进了PDLSCs的成骨分化。衰老相关β-半乳糖苷酶染色结果显示,0.1 μg/mL淫羊羊苷(ICA)和过表达WDR36抑制了PDLSCs的衰老,而WDR36缺失促进了PDLSCs的成骨分化。结论:WDR36能抑制PDLSCs的迁移、趋化、成骨分化和衰老;0.1 μg/mL ICA可抑制PDLSCs的衰老。因此,WDR36可能作为牙周组织再生和治疗牙周炎的靶点。
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来源期刊
World journal of stem cells
World journal of stem cells Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
7.80
自引率
4.90%
发文量
750
期刊介绍: The World Journal of Stem Cells (WJSC) is a leading academic journal devoted to reporting the latest, cutting-edge research progress and findings of basic research and clinical practice in the field of stem cells. It was launched on December 31, 2009 and is published monthly (12 issues annually) by BPG, the world''s leading professional clinical medical journal publishing company.
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