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

J Cell Mol Med. 2020 Jan;24(1):1076-1086. doi: 10.1111/jcmm.14832. Epub 2019 Nov 21.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation*
  • Fibroblasts / cytology*
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism
  • Fracture Healing / drug effects*
  • Fractures, Bone / drug therapy*
  • Fractures, Bone / metabolism
  • Fractures, Bone / pathology
  • Gene Expression Regulation
  • Interleukin-10 / pharmacology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • MicroRNAs / genetics
  • Osteoblasts / cytology*
  • Osteoblasts / drug effects
  • Osteoblasts / metabolism
  • Osteogenesis*
  • Receptor, IGF Type 1 / genetics
  • Receptor, IGF Type 1 / metabolism

Substances

  • IL10 protein, mouse
  • MicroRNAs
  • Interleukin-10
  • Receptor, IGF Type 1