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鸢尾素通过Wnt信号通路调节骨髓间充质干细胞的多能分化,重塑骨代谢稳态,从而延缓与年龄相关的骨质疏松症。

Irisin reshapes bone metabolic homeostasis to delay age-related osteoporosis by regulating the multipotent differentiation of BMSCs via Wnt pathway.

作者信息

Xing Shangman, Ma Yifan, Song Bing, Bai Min, Wang Kexin, Song Wenjing, Cao Tingting, Guo Chao, Zhang Yanying, Wang Zhandong, Wang Yongfeng

机构信息

The First Clinical Medical College, Gansu University of Chinese Medicine, Lanzhou, China.

Division of Cancer Biology, Laboratory Animal Center, Fourth Military Medical University, Xi'an, China.

出版信息

Front Mol Biosci. 2025 Jan 7;11:1524978. doi: 10.3389/fmolb.2024.1524978. eCollection 2024.

Abstract

INTRODUCTION

Bone aging is linked to changes in the lineage differentiation of bone marrow stem cells (BMSCs), which show a heightened tendency to differentiate into adipocytes instead of osteoblasts. The therapeutic potential of irisin in addressing age-related diseases has garnered significant attention. More significantly, irisin has the capacity to enhance bone mass recovery and sustain overall bone health. Its mechanism of action in preventing osteoporosis has generated considerable interest within the research community. Nonetheless, the targeting effect of irisin on age-related osteoporosis and its underlying molecular biological mechanisms remain unclear.

METHODS

The specific role of irisin in osteogenic-adipogenic differentiation in young or aging BMSCs was evaluated by multiple cells staining and quantitative real-time PCR (RT-qPCR) analysis. RNA-seq and protein Western blotting excavated and validated the key pathway by which irisin influences the fate determination of aging BMSCs. The macroscopic and microscopic changes of bone tissue in aging mice were examined using Micro-computed tomography (Micro-CT) and morphological staining.

RESULTS

It was noted that irisin affected the multilineage differentiation of BMSCs in a manner dependent on the dosage. Simultaneously, the Wnt signaling pathway might be a crucial mechanism through which irisin sustains the bone-fat balance in aging BMSCs and mitigates the decline in pluripotency. , irisin reduced bone marrow fat deposition in aging mice and effectively alleviating the occurrence of bone loss.

CONCLUSION

Irisin mediates the Wnt signaling pathway, thereby influencing the fate determination of BMSCs. In addition, it is essential for preserving metabolic equilibrium in the bone marrow microenvironment and significantly contributes to overall bone health. The findings provide new evidence for the use of iris extract in the treatment of age-related osteoporosis.

摘要

引言

骨老化与骨髓干细胞(BMSCs)谱系分化的变化有关,骨髓干细胞表现出向脂肪细胞而非成骨细胞分化的增强趋势。鸢尾素在解决与年龄相关疾病方面的治疗潜力已引起广泛关注。更重要的是,鸢尾素能够促进骨量恢复并维持整体骨骼健康。其预防骨质疏松症的作用机制在研究界引起了相当大的兴趣。然而,鸢尾素对年龄相关性骨质疏松症的靶向作用及其潜在的分子生物学机制仍不清楚。

方法

通过多细胞染色和定量实时PCR(RT-qPCR)分析评估鸢尾素在年轻或老化BMSCs成骨-脂肪生成分化中的具体作用。RNA测序和蛋白质免疫印迹挖掘并验证了鸢尾素影响老化BMSCs命运决定的关键途径。使用微型计算机断层扫描(Micro-CT)和形态学染色检查老化小鼠骨组织的宏观和微观变化。

结果

注意到鸢尾素以剂量依赖性方式影响BMSCs的多谱系分化。同时,Wnt信号通路可能是鸢尾素维持老化BMSCs骨-脂肪平衡并减轻多能性下降的关键机制。此外,鸢尾素减少了老化小鼠的骨髓脂肪沉积,并有效缓解了骨质流失的发生。

结论

鸢尾素介导Wnt信号通路,从而影响BMSCs的命运决定。此外,它对于维持骨髓微环境中的代谢平衡至关重要,并对整体骨骼健康有显著贡献。这些发现为使用鸢尾提取物治疗年龄相关性骨质疏松症提供了新的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1a7/11746060/97b75935f256/fmolb-11-1524978-g001.jpg

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