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血管内皮生长因子剂量控制工程骨中血管生成与骨生成的耦合。

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

作者信息

Grosso Andrea, Lunger Alexander, Burger Maximilian G, Briquez Priscilla S, Mai Francesca, Hubbell Jeffrey A, Schaefer Dirk J, Banfi Andrea, Di Maggio Nunzia

机构信息

Regenerative Angiogenesis Laboratory, Department of Biomedicine, Basel University Hospital and University of Basel, Hebelstrasse 20, 4031, Basel, Switzerland.

Department of Plastic, Reconstructive, Aesthetic and Hand Surgery, Basel University Hospital, Petersgraben 4, 4031, Basel, Switzerland.

出版信息

NPJ Regen Med. 2023 Mar 13;8(1):15. doi: 10.1038/s41536-023-00288-1.

Abstract

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.

摘要

血管内皮生长因子-A(VEGF)在生理上调节血管生成和成骨过程,但其在骨组织工程中的应用却产生了相互矛盾的结果。一个尚未得到充分理解的方面是VEGF剂量如何影响这两个过程之间的协调。利用一个独特且高度可调的平台,我们在此剖析了在组织工程化骨生成移植物的背景下,1000倍范围内VEGF剂量的影响。我们发现骨血管生成耦合高度依赖于VEGF剂量,只有严格定义的剂量范围才能刺激血管侵入和祖细胞的成骨定向分化,显著改善骨形成。此外,VEGF剂量调节Notch1激活以及特定促骨生成内皮表型的诱导,而与促进血管侵入无关。因此,从治疗角度来看,在信号微环境中微调VEGF剂量是确保加速血管侵入与改善骨形成的生理耦合的关键。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c55/10011536/411c2598e6b8/41536_2023_288_Fig1_HTML.jpg

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