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甜菜碱通过WDR81增强髁突软骨细胞前体细胞(SCAPs)的软骨形成分化并促进颞下颌关节骨关节炎(TMJOA)中的软骨修复。

Betaine enhances SCAPs chondrogenic differentiation and promotes cartilage repair in TMJOA through WDR81.

作者信息

Wang Meiyue, Wu Zejie, Zheng Xiaoyu, Huang Yishu, Jin Yizhou, Song Jiaxin, Lei Wanzhen, Liu Hua, Yu Riyue, Yang Haoqing, Gao Runtao

机构信息

Department of Stomatology, Beijing Friendship Hospital, Capital Medical University, Beijing, 100050, China.

Beijing Laboratory of Oral Health, Capital Medical University, Beijing, 100050, China.

出版信息

Stem Cell Res Ther. 2025 Feb 7;16(1):55. doi: 10.1186/s13287-025-04161-4.

Abstract

BACKGROUND

The cartilage tissue regeneration mediated with mesenchymal stem cells (MSCs) is considered as a viable strategy for temporomandibular joint osteoarthritis (TMJOA). Betaine has been confirmed to modulate the multidirectional differentiation of MSCs, while its effect on chondrogenic differentiation of Stem Cells from the Apical Papilla (SCAPs) is unknown. Here, we explored the effects and underlying mechanisms of betaine on chondrogenic differentiation of SCAPs.

METHODS

Betaine was added for SCAPs chondrogenic induction. The chondrogenic differentiation potential was assessed using Alcian Blue staining, Sirius Red staining and the main chondrogenic markers. In vivo cartilage regeneration effects were evaluated by the rat TMJOA model. RNA-sequencing and biological analyses were performed to select target genes and biological processes involved. The mechanism betaine acts on chondrogenic differentiation of SCAPs was further explored.

RESULTS

Betain-treated SCAPs demonstrated stronger cartilage regeneration in vitro and promoted cartilage repair of TMJOA in vivo. Betaine enhanced the expression of WDR81 in SCAPs during chondrogenesis. WDR81 overexpression promoted chondrogenic differentiation of SCAPs, while WDR81 depletion inhibited chondrogenic differentiation. In addition, both betaine treatment and WDR81 overexpression reduced intracellular reactive oxygen species levels and increased mitochondrial membrane potential in SCAPs.

CONCLUSION

Betaine promotes SCAPs chondrogenic differentiation and provided an effective candidate for TMJOA treatment. WDR81 may serve as the potential drug target through mitophagy.

摘要

背景

间充质干细胞(MSCs)介导的软骨组织再生被认为是颞下颌关节骨关节炎(TMJOA)的一种可行治疗策略。甜菜碱已被证实可调节MSCs的多向分化,但其对根尖乳头干细胞(SCAPs)成软骨分化的影响尚不清楚。在此,我们探讨了甜菜碱对SCAPs成软骨分化的影响及其潜在机制。

方法

添加甜菜碱进行SCAPs成软骨诱导。使用阿尔新蓝染色、天狼星红染色和主要成软骨标志物评估成软骨分化潜能。通过大鼠TMJOA模型评估体内软骨再生效果。进行RNA测序和生物学分析以选择相关的靶基因和生物学过程。进一步探讨甜菜碱作用于SCAPs成软骨分化的机制。

结果

经甜菜碱处理的SCAPs在体外表现出更强的软骨再生能力,并在体内促进了TMJOA的软骨修复。甜菜碱在成软骨过程中增强了SCAPs中WDR81的表达。WDR81过表达促进了SCAPs的成软骨分化,而WDR81缺失则抑制了成软骨分化。此外,甜菜碱处理和WDR81过表达均降低了SCAPs细胞内活性氧水平并增加了线粒体膜电位。

结论

甜菜碱促进SCAPs成软骨分化,为TMJOA治疗提供了一种有效的候选药物。WDR81可能通过线粒体自噬作为潜在的药物靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9c5/11806766/8d1bd1390b64/13287_2025_4161_Fig1_HTML.jpg

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