VEGF dose controls the coupling of angiogenesis and osteogenesis in engineered bone

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作者
Andrea Grosso
Alexander Lunger
Maximilian G. Burger
Priscilla S. Briquez
Francesca Mai
Jeffrey A. Hubbell
Dirk J. Schaefer
Andrea Banfi
Nunzia Di Maggio
机构
[1] Basel University Hospital and University of Basel,Regenerative Angiogenesis Laboratory, Department of Biomedicine
[2] Basel University Hospital,Department of Plastic, Reconstructive, Aesthetic and Hand Surgery
[3] University of Chicago,Pritzker School of Molecular Engineering
[4] Medical Center – University of Freiburg,Department of General and Visceral Surgery
[5] Faculty of Medicine,undefined
[6] University of Freiburg,undefined
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npj Regenerative Medicine | / 8卷
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摘要
Vascular endothelial growth factor-A (VEGF) physiologically regulates both angiogenesis and osteogenesis, but its application in bone tissue engineering led to contradictory outcomes. A poorly understood aspect is how VEGF dose impacts the coordination between these two processes. Taking advantage of a unique and highly tunable platform, here we dissected the effects of VEGF dose over a 1,000-fold range in the context of tissue-engineered osteogenic grafts. We found that osteo-angiogenic coupling is exquisitely dependent on VEGF dose and that only a tightly defined dose range could stimulate both vascular invasion and osteogenic commitment of progenitors, with significant improvement in bone formation. Further, VEGF dose regulated Notch1 activation and the induction of a specific pro-osteogenic endothelial phenotype, independently of the promotion of vascular invasion. Therefore, in a therapeutic perspective, fine-tuning of VEGF dose in the signaling microenvironment is key to ensure physiological coupling of accelerated vascular invasion and improved bone formation.
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