Suppr超能文献

一种高选择性 GSK-3β 抑制剂 CHIR99021 通过激活经典和自噬介导的 Wnt 信号促进成骨作用。

A Highly Selective GSK-3β Inhibitor CHIR99021 Promotes Osteogenesis by Activating Canonical and Autophagy-Mediated Wnt Signaling.

机构信息

Laboratory of Skeletal Development and Regeneration, Institute of Life Sciences, Chongqing Medical University, Chongqing, China.

出版信息

Front Endocrinol (Lausanne). 2022 Jul 18;13:926622. doi: 10.3389/fendo.2022.926622. eCollection 2022.

Abstract

The discovery and application of small molecules is one of the practical strategies of safe osteogenic drugs. The small molecule CHIR99021 (C91) is a highly specific, safe, and most effective GSK-3β Inhibitor. This study found that it efficiently activates the canonical Wnt signaling of bone marrow stromal cell ST2 and promotes osteoblast differentiation and mineralization. C91 increases the production and biochemical activity of osteoblast marker alkaline phosphatase, the expression of osteoblast marker genes , and , and the formation of bone nodules. Triptonide is a transcription inhibitor of Wnt target gene, which diminishes C91-induced osteoblast differentiation in a dose-dependent manner. Meanwhile, C91 also induces autophagy through autophagosome formation and conversion of autophagy biomarker LC-3I into LC-3II. Autophagy inhibitor 3MA partially reduces C91-induced osteoblast differentiation and mineralization; autophagy inducer Rapamycin increases the expression of β-catenin to promote osteogenic differentiation, but cannot alleviate the inhibition of Triptonide on C91-induced osteogenic differentiation, indicating the crosstalk of canonical Wnt signaling and autophagy regulates C91-induced osteoblast differentiation. Furthermore, in order to simulate the detection of C91 in osteogenesis process, we made a C91 slow-release hydrogel with our newly established polycaprolactone and cell-integrated 3D printing system (PCCI3D module). The sustained release C91 promotes the differentiation and mineralization of ST2 cells. C91 can also enhance the proliferative activity of ST2 cells. The release rate of C91 from hydrogel gradually decreases within 7 days. During this period, the C91 is released by 83.0% and the cell viability maintained at 96.4%. Therefore, the small molecule Wnt agonist C91 promotes osteogenesis through caonical and autophagy-mediated Wnt signaling pathway with an option for translational application.

摘要

小分子的发现和应用是安全成骨药物的实用策略之一。小分子 CHIR99021(C91)是一种高度特异、安全、最有效的 GSK-3β抑制剂。本研究发现,它能有效激活骨髓基质细胞 ST2 的经典 Wnt 信号通路,促进成骨细胞分化和矿化。C91 增加碱性磷酸酶等成骨细胞标记物的产生和生化活性,上调成骨细胞标记基因的表达,并形成骨结节。雷公藤内酯酮是 Wnt 靶基因的转录抑制剂,能呈剂量依赖性减弱 C91 诱导的成骨细胞分化。同时,C91 还通过自噬体形成和自噬标志物 LC-3I 转化为 LC-3II 诱导自噬。自噬抑制剂 3MA 部分减少 C91 诱导的成骨细胞分化和矿化;自噬诱导剂雷帕霉素增加 β-连环蛋白的表达以促进成骨分化,但不能缓解雷公藤内酯酮对 C91 诱导的成骨分化的抑制作用,表明经典 Wnt 信号和自噬的串扰调节 C91 诱导的成骨细胞分化。此外,为了模拟 C91 在成骨过程中的检测,我们利用我们新建立的聚己内酯和细胞整合的 3D 打印系统(PCCI3D 模块)制作了 C91 缓释水凝胶。持续释放的 C91 促进 ST2 细胞的分化和矿化。C91 还能增强 ST2 细胞的增殖活性。C91 从水凝胶中的释放率在 7 天内逐渐降低,在此期间,C91 以 83.0%的释放率释放,细胞活力保持在 96.4%。因此,小分子 Wnt 激动剂 C91 通过经典 Wnt 信号通路和自噬途径促进成骨作用,为转化应用提供了选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23d0/9339598/3f37a7ae734e/fendo-13-926622-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验