Dental pulp stem cell-derived intracellular vesicles prevent orthodontic relapse by inhibiting PI3K/Akt/NF-κB-mediated osteoclast activity

被引:0
|
作者
Peng, Boyuan [1 ]
Li, Ziwei [3 ]
Cheng, Yong [1 ]
Jiang, Henghua [1 ,2 ]
Ye, Qingsong [3 ,4 ]
Han, Guangli [1 ,2 ]
机构
[1] Wuhan Univ, State Key Lab Oral & Maxillofacial Reconstruct & R, Key Lab Oral Biomed, Minist Educ,Hubei Key Lab Stomatol,Sch & Hosp Stom, 237 Luoyu Rd, Wuhan City 430079, Peoples R China
[2] Wuhan Univ, Sch & Hosp Stomatol, Dept Orthodont, Div 2, Wuhan 430079, Peoples R China
[3] Wuhan Univ, Renmin Hosp, Ctr Regenerat Med, Dept Stomatol, Gaoxin 6th Rd, Wuhan 430000, Hubei, Peoples R China
[4] Univ Sydney, Sydney Sch Dent, Sydney, NSW, Australia
基金
中国国家自然科学基金;
关键词
Orthodontic tooth movement; Intercellular vesicles; Bone remodeling; Oral medicine; Stem cells; Cell communication; IN-VITRO; EXPRESSION; EXOSOMES; DIFFERENTIATION;
D O I
10.1186/s13287-025-04146-3
中图分类号
Q813 [细胞工程];
学科分类号
摘要
BackgroundOrthodontic relapse, the undesired deviation of teeth from their corrected positions, remains a significant challenge in clinical orthodontics. Incomplete periodontal bone remodeling has been identified as a key factor in this process. Despite decades of research, currently there are no effective strategies to prevent relapse.MethodsWe isolated and identified dental pulp stem cell-derived intracellular vesicles (DPSC-IV) from human dental pulp tissue. To investigate its effect, DPSC-IV was added to osteoblast or osteoclast differentiation medium. During the orthodontic retention period, DPSC-IV was administrated to rats by subgingival injection. Relapse distance and relapse rate were calculated to evaluate DPSC-IV's ability to prevent relapse. Additionally, Western blot analysis were used to examine DPSC-IV's inhibitory effect on osteoclast differentiation.ResultsDPSC-IV significantly promoted osteoblast differentiation and inhibited osteoclast differentiation. Application of DPSC-IV during retention resulted in a significant reduction in both relapse distance and relapse rate, with improved periodontal structure and decreased osteoclast activity. This effect was mediated by the PI3K/Akt/NF-kappa B signaling pathway and could be reversed by the PI3K activator insulin-like growth factor-1 (IGF-1).ConclusionThis study highlights the potential of DPSC-IV as a novel preventive approach against orthodontic relapse, offering a novel strategy for maintaining long-term orthodontic stability.
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页数:14
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