IL-10 induces MC3T3-E1 cells differentiation towards osteoblastic fate in murine model

IL-10在小鼠模型中诱导MC3T3-E1细胞向成骨细胞分化

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作者:Yuan Xiong ,Chenchen Yan ,Lang Chen ,Yori Endo ,Yun Sun ,Wu Zhou ,Yiqiang Hu ,Liangcong Hu ,Dong Chen ,Hang Xue ,Bobin Mi ,Guohui Liu

Abstract

Interleukin-10 (IL-10) displays well-documented anti-inflammatory effects, but its effects on osteoblast differentiation have not been investigated. In this study, we found IL-10 negatively regulates microRNA-7025-5p (miR-7025-5p), the down-regulation of which enhances osteoblast differentiation. Furthermore, through luciferase reporter assays, we found evidence that insulin-like growth factor 1 receptor (IGF1R) is a miR-7025-5p target gene that positively regulates osteoblast differentiation. In vivo studies indicated that the pre-injection of IL-10 leads to increased bone formation, while agomiR-7025-5p injection delays fracture healing. Taken together, these results indicate that IL-10 induces osteoblast differentiation via regulation of the miR-7025-5p/IGF1R axis. IL-10 therefore represents a promising therapeutic strategy to promote fracture healing. Keywords: Fracture; IGF1R; IL-10; mRNA; miRNA; osteoblast.

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