机械敏感通道
脂肪生成
细胞生物学
间充质干细胞
压电1
化学
运行x2
条件基因敲除
基质(化学分析)
细胞外基质
骨细胞
成骨细胞
机械转化
软骨发生
生物
自愈水凝胶
信号转导
软骨细胞
硫氧化物9
基质金属蛋白酶
再生医学
细胞分化
骨形态发生蛋白
干细胞
Cre-Lox重组
转录因子
下调和上调
谱系(遗传)
解剖
骨形态发生蛋白2
作者
Shuo Zhang,Siteng Li,Wenzhong Chen,Wenzhong Chen,Qingcheng Song,Haiyue Zhao,Peng Wang,Yiran Zhang,Yiran Zhang,Wenquan Liang,Shaowei Zheng,Juan Wang,Wei Chen,Wei Chen,Yanbin Zhu,Yingze Zhang,Yingze Zhang
摘要
ABSTRACT Mesenchymal stem cells (MSCs) are critical for bone regeneration, and their osteogenic and adipogenic lineage balance is intricately regulated by cellular mechanotransduction. Through single‐cell RNA sequencing reanalysis of the public dataset GSE166824, primary mouse MSC functional assays, and in vivo genetic and bone defect models, this study identifies a novel PIEZO1/specificity protein 1 (SP1)/stanniocalcin 2 (STC2) signaling axis that drives matrix stiffness‐dependent MSC lineage commitment. Stiff matrices robustly direct MSCs toward osteogenic differentiation while inhibiting adipogenesis by activating the mechanosensitive ion channel PIEZO1. PIEZO1 activation triggers Ca 2 + influx, leading to calcium/calmodulin‐dependent protein kinase II (CaMKII)‐dependent SP1 activation. SP1 shows enrichment at the promoter region of Stc2 and upregulates its expression. The secreted protein STC2 functions downstream of PIEZO1 on stiff matrices while retaining pro‐osteogenic and anti‐adipogenic activity when PIEZO1 remains inactive. In a mouse femoral bone defect model under hindlimb unloading, both stiff gelatin methacryloyl (GelMA) hydrogels and exogenous STC2 administration enhance early‐stage bone formation on day 7. Conversely, Prrx1 ‐lineage‐specific inducible conditional knockout (iCKO) of Piezo1 abrogates the regulatory effects of matrix stiffness. These findings establish the PIEZO1/SP1/STC2 axis as a pivotal mechanosensitive signaling pathway for MSC fate determination, offering novel molecular targets for mechanically optimized bone regenerative biomaterials.
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