Bidirectional regulation between bone and vasculature: Mechanisms of osteogenesis and angiogenesis

Tianyue Wang1, Hanbing Yao2, Feier Jin3

  • 1Department of Orthopaedic Surgery, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou 310016, China; Zhejiang Key Laboratory of Mechanism Research and Precision Repair of Orthopaedic Trauma and Aging Diseases, Hangzhou 310016, China.

PubMed

Insights

This review explores the crucial bone-vascular crosstalk, revealing how osteogenic and vascular cells communicate. Targeting this interaction offers new therapeutic strategies for bone diseases like osteoporosis.

Area of Science:

  • Bone biology and vascular biology
  • Skeletal homeostasis and disease mechanisms
  • Molecular regulation of bone and vasculature

Background:

  • The skeletal and vascular systems are intricately linked, maintaining bone homeostasis through distinct mechanisms in intramembranous and endochondral ossification.
  • Imbalances in this bidirectional regulation contribute to bone pathologies such as osteoporosis, osteoarthritis, and rheumatoid arthritis.

Purpose of the Study:

  • To dissect the molecular networks governing bone-vascular crosstalk.
  • To clarify the physiological and pathological regulatory mechanisms involved.
  • To highlight the therapeutic potential of targeting the vascular microenvironment for bone diseases.

Main Methods:

  • Review of existing literature on bone-vascular interactions.
  • Analysis of molecular signaling pathways (e.g., VEGF, PDGF, miRNAs, BMP-SMAD, Notch, HIF).
  • Discussion of therapeutic strategies targeting the bone-vascular interface.

Main Results:

  • Osteogenic cells regulate angiogenesis through pathways including VEGF, PDGF, and miRNAs.
  • Vascular endothelial cells modulate osteogenesis via BMP-SMAD, Notch, and HIF signaling.
  • Bone-vascular crosstalk is a key factor in both normal bone metabolism and disease pathogenesis.

Conclusions:

  • Understanding bone-vascular crosstalk is essential for addressing bone diseases.
  • Targeting the vascular microenvironment presents a promising avenue for novel therapeutic interventions.
  • This review provides a foundation for translational research in precision therapies for bone diseases.
Abstract

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