血管生成
Notch信号通路
血流
平衡
血管
细胞生物学
医学
生物
癌症研究
内分泌学
内科学
信号转导
作者
Saravana K. Ramasamy,Anjali P. Kusumbe,Maria Schiller,Dagmar Zeuschner,M. Gabriele Bixel,C. Fernandez Milia,Jaba Gamrekelashvili,Anne Limbourg,Alexander Medvinsky,Massimo Santoro,Florian P. Limbourg,Ralf H. Adams
摘要
Abstract While blood vessels play important roles in bone homeostasis and repair, fundamental aspects of vascular function in the skeletal system remain poorly understood. Here we show that the long bone vasculature generates a peculiar flow pattern, which is important for proper angiogenesis. Intravital imaging reveals that vessel growth in murine long bone involves the extension and anastomotic fusion of endothelial buds. Impaired blood flow leads to defective angiogenesis and osteogenesis, and downregulation of Notch signalling in endothelial cells. In aged mice, skeletal blood flow and endothelial Notch activity are also reduced leading to decreased angiogenesis and osteogenesis, which is reverted by genetic reactivation of Notch. Blood flow and angiogenesis in aged mice are also enhanced on administration of bisphosphonate, a class of drugs frequently used for the treatment of osteoporosis. We propose that blood flow and endothelial Notch signalling are key factors controlling ageing processes in the skeletal system.
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