SIRT1 activation promotes bone repair by enhancing the coupling of type H vessel formation and osteogenesis

Cell Prolif. 2024 Jun;57(6):e13596. doi: 10.1111/cpr.13596. Epub 2024 Jan 11.

Abstract

Bone repair is intricately correlated with vascular regeneration, especially of type H vessels. Sirtuin 1 (SIRT1) expression is closely associated with endothelial function and vascular regeneration; however, the role of SIRT1 in enhancing the coupling of type H vessel formation with osteogenesis to promote bone repair needs to be investigated. A co-culture system combining human umbilical vein endothelial cells and osteoblasts was constructed, and a SIRT1 agonist was used to evaluate the effects of SIRT1 activity. The angiogenic and osteogenic capacities of the co-culture system were examined using short interfering RNA. Mouse models with bone defects in the femur or mandible were established to explore changes in type H vessel formation and bone repair following modulated SIRT1 activity. SIRT1 activation augmented the angiogenic and osteogenic capacities of the co-culture system by activating the PI3K/AKT/FOXO1 signalling pathway and did not significantly regulate osteoblast differentiation. Inhibition of the PI3K/AKT/FOXO1 pathway attenuated SIRT1-mediated effects. The SIRT1 activity in bone defects was positively correlated with the formation of type H vessels and bone repair in vivo, whereas SIRT1 inhibition substantially weakened vascular and bone formation. Thus, SIRT1 is crucial to the coupling of type H vessels with osteogenesis during bone repair.

MeSH terms

  • Animals
  • Bone Regeneration
  • Cell Differentiation
  • Coculture Techniques*
  • Forkhead Box Protein O1 / metabolism
  • Human Umbilical Vein Endothelial Cells* / metabolism
  • Humans
  • Mice
  • Mice, Inbred C57BL
  • Neovascularization, Physiologic
  • Osteoblasts* / cytology
  • Osteoblasts* / metabolism
  • Osteogenesis* / physiology
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Signal Transduction*
  • Sirtuin 1* / genetics
  • Sirtuin 1* / metabolism

Substances

  • Forkhead Box Protein O1
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-akt
  • SIRT1 protein, human
  • Sirtuin 1
  • Sirt1 protein, mouse