软骨内骨化
软骨细胞
骨愈合
骨不连
软骨
压电1
衰老
软骨发生
细胞生物学
医学
解剖
内科学
受体
生物
机械敏感通道
离子通道
作者
Siming Jia,Weijian Liu,Mo Zhang,Lijun Wang,Chuan Ren,Feng Chen,Tao Zhang,Hongzhi Lv,Zhiyong Hou,Weiguo Zou,Ying‐ze Zhang,Wei Tong,Juan Wang,Wei Chen
标识
DOI:10.1002/advs.202400502
摘要
Abstract Insufficient mechanical loading impairs fracture healing; however, the underlying mechanisms remain unclear. Increasing evidence indicates that Piezo1 plays an important role in fracture healing, although the effect of Piezo1 on the endochondral ossification of chondrocytes has been overlooked. This study reports that mechanical unloading down‐regulates the expression of Piezo1 in chondrocytes and leads to fracture nonunion. Single‐cell sequencing of calluses revealed that specific deletion of Piezo1 in chondrocytes upregulated the expression of apolipoprotein E (ApoE) in hypertrophic chondrocytes, resulting in delayed cartilage‐to‐bone transition due to enhanced chondrocyte senescence. Based on these results, an injectable and thermosensitive hydrogel is developed, which released an ApoE antagonist in situ at the fracture site. This hydrogel effectively attenuated chondrocyte senescence and, thus, promoted cartilage‐to‐bone transition as well as the fracture healing process. Overall, this data provide a new perspective on the activity of chondrocytes in fracture healing and a new direction for the treatment of fracture nonunion caused by insufficient mechanical loading.
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