载牙源性间充质干细胞水凝胶在牙周组织修复中的应用研究进展OA
Research progress on the application of dental originated mesenchymal stem cell hydrogel in periodontal tis-sue repair
牙周组织的完全性功能再生(即牙槽骨、牙骨质与牙周韧带的同步重建)是口腔再生医学面临的重大挑战.牙源性间充质干细胞(DMSCs)因其多向分化潜能与免疫调节特性,是实现这一目标的理想种子细胞.水凝胶作为细胞载体,其核心优势在于能够通过精确调控的理化性质(如基质硬度、拓扑结构、降解动力学)模拟细胞外基质,构建主动调控干细胞命运的力学与生化微环境.本文综述了载DMSCs水凝胶在牙周组织修复中的应用与研究进展.文章首先分析了不同水凝胶体系的材料学特性,进而重点阐述了水凝胶通过基质硬度等力学属性调控DMSCs分化的具体分子机制:刚性水凝胶通过激活整合素-粘着斑激酶(FAK)-蛋白激酶B(Akt)哺乳动物雷帕霉素靶蛋白(mTOR)信号轴驱动成骨分化;诱导细胞骨架重构,促使Yes相关蛋白(YAP)/转录共激活因子PDZ结合基序(TAZ)去磷酸化并发生核转位,启动成骨相关基因的转录;同时稳定Wnt/β连环蛋白(Wnt/β-catenin)并激活Wnt信号通路,上调Runt相关转录因子2(Runx2)及Osterix等成骨关键转录因子的表达.此外,作为生物活性因子的程序化控释载体,水凝胶能够选择性激活 Smad 家族蛋白(Smad)信号亚型,促成骨因子特异性激活Smad1/5/8通路,促牙周韧带形成因子则激活Smad2/3通路,从而实现DMSCs向成骨、成牙骨质或成纤维谱系的精准定向分化.目前,该领域面临的关键科学问题包括水凝胶性能在再生过程中的动态适配、复杂口腔微环境(如微生物、机械力、炎症)的稳定控制、干细胞高效定向分化策略以及临床转化可行性.未来研究方向将集中于开发智能响应型水凝胶、结合3D生物打印技术构建个性化仿生支架,以及设计具有免疫调控功能的复合材料体系,以期最终实现牙周组织的结构与功能一体化再生.
The complete functional regeneration of periodontal tissues—specifically,the simultaneous reconstruc-tion of alveolar bone,cementum,and periodontal ligament—represents a major challenge in oral regenerative medicine.Dental-derived mesenchymal stem cells(DMSCs)are regarded as ideal seed cells for achieving this goal due to their multi-lineage differentiation potential and immunomodulatory properties.As a cell carrier,hydrogels offer the key ad-vantage of mimicking the extracellular matrix through precisely tunable physicochemical properties(e.g.,matrix stiff-ness,topological structure,degradation kinetics),thereby constructing a mechanical and biochemical microenvironment that actively directs stem cell fate.This review summarizes the application and research progress of DMSC-laden hydro-gels in periodontal tissue repair.We first analyze the material characteristics of different hydrogel systems,and then elaborate on the specific molecular mechanisms by which hydrogels regulate DMSCs'differentiation through mechani-cal properties such as matrix stiffness:stiff hydrogels drive osteogenic differentiation by activating the integrin-focal ad-hesion kinase(FAK)-Akt/mechanistic target of rapamycin(mTOR)signaling axis;inducing cytoskeletal remodeling,and promoting dephosphorylation and nuclear translocation of Yes-associated protein(YAP)/transcriptional co-activator with PDZ-binding motif(TAZ)to initiate the transcription of osteogenesis-related genes;and stabilizing β-catenin and activating the Wnt/β-catenin signaling pathway,upregulating the expression of key osteogenic transcription factors in-cluding Runt-related transcription factor 2(Runx2)and Osterix.Furthermore,as programmed controlled-release carriers for bioactive factors,hydrogels selectively activate Smad signaling subtypes—pro-osteogenic factors specifically activate the Smad1/5/8 pathway,whereas factors promoting periodontal ligament formation activate the Smad2/3 pathway—thereby achieving precise,directed differentiation of DMSCs toward osteogenic,cementogenic,or fibroblastic lineages.Current key scientific issues in this field include the dynamic adaptation of hydrogel properties during regeneration,stable control of the complex oral microenvironment(e.g.,microbes,mechanical forces,inflammation),strategies for effi-cient directional differentiation of stem cells,and feasibility of clinical translation.Future research directions should focus on developing smart-responsive hydrogels,constructing personalized biomimetic scaffolds combined with three-dimensional bioprinting technology,and designing composite material systems with immunomodulatory functions,aim-ing ultimately to achieve integrated structural and functional regeneration of periodontal tissue.
李群;夏春鹏;张男
山东第一医科大学(山东省医学科学院)口腔医学院,山东 济南(250117)山东第一医科大学附属聊城医院(聊城市人民医院)口腔正畸科,山东 聊城(252000)山东省医药卫生干细胞与再生医学转化重点实验室,聊城市人民医院,山东 聊城(252000)
医药卫生
牙源性间充质干细胞水凝胶基质硬度力学转导牙周组织再生力学微环境牙周炎组织工程三维支架
dental-derived mesenchymal stem cellshydrogelmatrix stiffnessmechanotransductionperi-odontal tissue regenerationmechanical microenvironmentperiodontitistissue engineeringthree-dimensional scaffold
《口腔疾病防治》 2026 (7)
720-730,11
山东省自然科学基金面上项目(ZR2024MH132)山东省医药卫生科技项目(202308051068)鲁渝科技协作计划项目(2022LYXZ022)聊城市重点研发计划政策引导类项目(2023YD41)山东第二医科大学附属医院科技发展项目(2023FYM1078)山东第二医科大学科研发展基金(2024FYM117). This study was supported by the grants from Shandong Provincial Natural Science Foundation General Project(No.ZR2024MH132)Shandong Provincial Medical and Health Science Proj-ect(No.202308051068)Lu Yu Science and Technology Cooperation Project(No.2022LYXZ022)Liaocheng Key Research and Development Program Policy Guidance Project(No.2023YD41)Shandong Second Medical University Affiliated Hospital Science and Technology Develop-ment Project(No.2023FYM1078)Shandong Second Medical University Research Development Fund(No.2024FYM117).The funder had no role in the study design,data collection and analysis,decision to pub-lish,or preparation of the manuscript.
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