The osteo-angiogenic signaling crosstalk for bone regeneration: harmony out of complexity

被引:38
作者
Di Maggio, Nunzia [1 ,2 ]
Banfi, Andrea [1 ,2 ,3 ]
机构
[1] Basel Univ Hosp, Dept Biomed, Cell & Gene Therapy, Basel, Switzerland
[2] Univ Basel, Basel, Switzerland
[3] Basel Univ Hosp, Plast Reconstruct Aesthet & Hand Surg, Basel, Switzerland
基金
欧盟地平线“2020”; 瑞士国家科学基金会;
关键词
ENDOTHELIAL GROWTH-FACTOR; VEGF; DIFFERENTIATION; OSTEOGENESIS; RECEPTOR; OSTEOPROTEGERIN; CELLS;
D O I
10.1016/j.copbio.2022.102750
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In recent years it has been increasingly appreciated that blood vessels are not simply suppliers of nutrients and oxygen, but actually play an exquisite regulatory role in bone development and repair. A specialized kind of endothelium, named type H because of its high expression of CD31 and Endomucin, constitutes anatomically defined vessels in proximity of the epiphyseal growth plate. Type H endothelium regulates the proliferation and differentiation of both osteoblasts and osteoclasts through the secretion of angiocrine signals and is a hub for the bidirectional molecular crosstalk between the different cell populations of the osteogenic microenvironment. Type H vessels are a key target for current translational approaches aiming at coupling angiogenesis and osteogenesis for bone repair. Open questions remain about their presence and features in notstereotyped tissues, like engineered osteogenic grafts, and the opportunities for their clinical stimulation by pharmacological treatments.
引用
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页数:6
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