Cellular Senescence in Craniofacial Tissue Regeneration: Inducers, Biomarkers, and Interventions

被引:0
|
作者
Tang, Weibing [1 ,2 ]
Huo, Fangjun [1 ]
Long, Jie [2 ]
Zhang, Siyuan [1 ]
Tian, Weidong [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp Stomatol, Natl Clin Res Ctr Oral Dis, Engn Res Ctr Oral Translat Med,State Key Lab Oral, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp Stomatol, Dept Oral & Maxillofacial Surg, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金;
关键词
cell senescence; mesenchymal stem cells; craniofacial tissues; tissue engineering; MESENCHYMAL STEM-CELLS; OXIDATIVE STRESS; OSTEOGENIC DIFFERENTIATION; SECRETORY PHENOTYPE; INHIBITS APOPTOSIS; TELOMERE LENGTH; DAMAGE; AUTOPHAGY; LIPOFUSCIN; TARGET;
D O I
10.1089/ten.teb.2023.0136
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Craniofacial defects and dental tissue loss have significant negative impacts on the structure and function of jaws and face, often resulting in psychological issues in patients, emphasizing the urgent need for effective craniofacial tissue reconstruction. Unfortunately, natural regeneration of these tissues is limited. Dental-derived mesenchymal stem cells (MSCs) have emerged as a promising resource for tissue engineering-based therapeutic approaches. However, the clinical outcomes of MSC-based transplantation have not met expectations due to various complex reasons, and cellular senescence is recognized as one of the potential mechanisms contributing to the suboptimal results. The quality of MSC decreases during large-scale in vitro expansion, and it is also influenced by the age and the health status of donors. To address these challenges, extensive efforts have been made to developing strategies to combat senescence in tissue engineering, leveraging on current knowledge of underlying mechanisms. This review aims to elucidate the impact of cell senescence in craniofacial and dental regeneration and provides an overview of state-of-the-art antisenescence strategies. We first discuss the potential factors that trigger cell senescence in craniofacial tissue engineering. Then we describe senescence biomarkers, monitoring methods for senescent MSCs, and their underlying molecular mechanisms. The primary focus of this review is on current strategies to inhibit and alleviate cell senescence in tissue engineering. We summarize the strategies concerning the prevention of cell senescence, senolysis, modulation of the senescent associated secretory phenotype, and reversal of senescent MSCs, offering promising opportunities to overcome the challenges associated with cell senescence in craniofacial tissue engineering. Impact statementCellular senescence presents a significant hurdle in harnessing the full potential of mesenchymal stem cells (MSCs) for therapeutic applications. This review focuses on exploring the impact of MSC senescence on craniofacial tissue regeneration. We include the latest advancements in senescence triggers, specific biomarkers, and detection methods. Furthermore, we summarize state-of-the-art antisenescence strategies, categorized as prevention interventions, senolysis, modulation of the senescent-associated secretory phenotype, and reversal of senescent MSCs. This review offers valuable insights into the role of cell senescence in craniofacial tissue regeneration and suggests potential directions for future research and therapeutic interventions.
引用
收藏
页码:128 / 141
页数:14
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