Jia Linglu, Xiao Han, Hao Zhenghao, Sun Shaoqing, Zhao Wenxi, Gong Zikai, Gu Weiting, Wen Yong
School and Hospital of Stomatology, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, China; Shandong Key Laboratory of Oral Tissue Regeneration & Shandong Engineering Research Center of Dental Materials and Oral Tissue Regeneration, Jinan, Shandong, China; Shandong Provincial Clinical Research Center for Oral Diseases, Jinan, Shandong, China.
Department of Obstetrics and Gynecology, Qilu Hospital of Shandong University, China.
Biochim Biophys Acta Mol Cell Res. 2025 Mar;1872(3):119921. doi: 10.1016/j.bbamcr.2025.119921. Epub 2025 Feb 17.
Periodontal ligament stem cell (PDLSC)-based tissue engineering is an important method to promote periodontal tissue regeneration. However, PDLSCs are susceptible to the effects of replicative senescence, leading to reduced proliferation and differentiation abilities and weakened tissue regeneration potential. Senolytics (the combination of dasatinib and quercetin) are drugs that inhibit cellular aging through inducing the apoptosis of senescent cells, but whether they have positive effects during the senescence of PDLSCs is unknown. The present study established a long-term in vitro culture model of PDLSCs and then analyzed the effects of senolytics on the senescence, apoptosis, and osteogenic differentiation of PDLSCs in vitro and PDLSC-based tissue regeneration in vivo. The results showed that senolytics delayed the process of aging in prolonged-cultured PDLSCs and promoted the elimination and apoptosis of senescent cells. Moreover, senolytics improved the osteogenic differentiation ability of both young and senescent PDLSCs in vitro and promoted PDLSC-based alveolar bone regeneration in vivo. Furthermore, senolytics inhibited the expression of YAP in senescent PDLSCs. Their antiaging effects were enhanced when combined with the YAP inhibitor verteporfin, but were inhibited when combined with the YAP activator NIBR-LTSi. Taken together, these findings suggest that senolytics promoted the elimination of senescent PDLSCs and enhanced senescent PDLSC-based bone regeneration, partially through the inhibition of YAP expression.
基于牙周膜干细胞(PDLSC)的组织工程是促进牙周组织再生的重要方法。然而,PDLSCs易受复制性衰老的影响,导致增殖和分化能力降低,组织再生潜力减弱。衰老细胞溶解剂(达沙替尼和槲皮素的组合)是通过诱导衰老细胞凋亡来抑制细胞衰老的药物,但它们在PDLSCs衰老过程中是否具有积极作用尚不清楚。本研究建立了PDLSCs的长期体外培养模型,然后分析了衰老细胞溶解剂对PDLSCs体外衰老、凋亡和成骨分化以及体内基于PDLSC的组织再生的影响。结果表明,衰老细胞溶解剂延缓了长期培养的PDLSCs的衰老过程,促进了衰老细胞的清除和凋亡。此外,衰老细胞溶解剂在体外提高了年轻和衰老PDLSCs的成骨分化能力,并在体内促进了基于PDLSC的牙槽骨再生。此外,衰老细胞溶解剂抑制了衰老PDLSCs中YAP的表达。当与YAP抑制剂维替泊芬联合使用时,它们的抗衰老作用增强,但与YAP激活剂NIBR-LTSi联合使用时则受到抑制。综上所述,这些发现表明衰老细胞溶解剂促进了衰老PDLSCs的清除,并增强了基于衰老PDLSC的骨再生,部分是通过抑制YAP表达实现的。