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.
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.
Background:
The skeletal and vascular systems exhibit critical bidirectional regulation essential for skeletal homeostasis, with distinct mechanisms in intramembranous and endochondral ossification. Disruption of this balance triggers bone diseases like osteoporosis, osteoarthritis, and rheumatoid arthritis.
Aim Of Review:
This review aims to dissect the molecular networks of bone-vascular crosstalk, clarify its physiological/pathological regulatory mechanisms, emphasize the therapeutic value of targeting the vascular microenvironment, and provide perspectives for bone disease translational research. Key Scientific Concepts of Review: This work discusses bone-vascular interactions in normal and diseased states, highlighting that osteogenic cells regulate angiogenesis via VEGF/PDGF/miRNAs, while vascular endothelial cells modulate osteogenesis through BMP-SMAD/Notch/HIF pathways. Targeting this crosstalk can intervene in bone pathologies, laying a foundation for precision therapies for bone diseases.
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