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

Y Xiong, C Yan, L Chen, Y Endo, Y Sun… - Journal of cellular …, 2020 - Wiley Online Library
Y Xiong, C Yan, L Chen, Y Endo, Y Sun, W Zhou, Y Hu, L Hu, D Chen, H Xue, B Mi, G Liu
Journal of cellular and molecular medicine, 2020Wiley Online Library
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 …
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.
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