Zhang Lulu, Ji Caixia, Li Ziyun, Jiwa Habu, Xie Zhou, Luo Xiaoji, Luo Jinyong
Key Laboratory of Diagnostic Medicine Designated by the Chinese Ministry of Education, Chongqing Medical University, Chongqing 40016, China.
Department of Clinical Laboratory, People's Hospital of Deyang City, Deyang, Sichuan 618000, China.
Genes Dis. 2024 Apr 14;12(3):101308. doi: 10.1016/j.gendis.2024.101308. eCollection 2025 May.
Bone morphogenetic protein 9 (BMP9) has remarkable potential to induce the differentiation of mesenchymal stem cells (MSCs) towards the osteoblastic lineage. Additionally, research suggests that certain growth factors have the ability to potentiate BMP9-induced osteogenic differentiation of MSCs. Sonic Hedgehog (Shh) plays an indispensable role in the regulation of skeletal development. The objective of this research was to assess the potential influence of Shh on BMP9-induced osteogenic differentiation of MSCs. Our findings indicated that Shh effectively enhanced BMP9-induced early and late osteogenic differentiation of MSCs, and increased BMP9-induced expression/transcriptional activity of osteogenesis-related transcription factors. Besides, it was observed that Shh promoted BMP9-induced ectopic bone formation of MSCs . Moreover, BMP9 was able to facilitate the repair of bone defects in rats, while Shh further accelerated this reparative process. Mechanistically, Shh enhanced the activation of the Smad1/5/8 signaling pathway which was induced by BMP9. Furthermore, GANT-61, an inhibitor of Gli1 and Gli2, attenuated the enhancing effect of Shh on BMP9-induced osteogenic differentiation of MSCs. Collectively, the co-administration of BMP9 and Shh may present a promising therapeutic approach for the treatment of fracture nonunion, delayed fracture healing, and bone defects.
骨形态发生蛋白9(BMP9)具有显著的诱导间充质干细胞(MSCs)向成骨细胞谱系分化的潜力。此外,研究表明某些生长因子有能力增强BMP9诱导的MSCs成骨分化。音猬因子(Shh)在骨骼发育的调控中发挥着不可或缺的作用。本研究的目的是评估Shh对BMP9诱导的MSCs成骨分化的潜在影响。我们的研究结果表明,Shh有效地增强了BMP9诱导的MSCs早期和晚期成骨分化,并增加了BMP9诱导的成骨相关转录因子的表达/转录活性。此外,观察到Shh促进了BMP9诱导的MSCs异位骨形成。而且,BMP9能够促进大鼠骨缺损的修复,而Shh进一步加速了这一修复过程。机制上,Shh增强了BMP9诱导的Smad1/5/8信号通路的激活。此外,Gli1和Gli2的抑制剂GANT-61减弱了Shh对BMP9诱导的MSCs成骨分化的增强作用。总的来说,联合使用BMP9和Shh可能为治疗骨折不愈合、骨折延迟愈合和骨缺损提供一种有前景的治疗方法。