Blood flow controls bone vascular function and osteogenesis

被引:337
作者
Ramasamy, Saravana K. [1 ,2 ,3 ]
Kusumbe, Anjali P. [1 ,2 ,4 ]
Schiller, Maria [1 ,2 ]
Zeuschner, Dagmar [5 ]
Bixel, M. Gabriele [1 ,2 ]
Milia, Carlo [6 ]
Gamrekelashvili, Jaba [7 ]
Limbourg, Anne [8 ]
Medvinsky, Alexander [9 ]
Santoro, Massimo M. [6 ,10 ]
Limbourg, Florian P. [7 ]
Adams, Ralf H. [1 ,2 ]
机构
[1] Max Planck Inst Mol Biomed, Dept Tissue Morphogenesis, Fac Med, D-48149 Munster, Germany
[2] Univ Munster, D-48149 Munster, Germany
[3] Imperial Coll London, Inst Clin Sci, Res Grp Integrat Skeletal Physiol, Hammersmith Hosp Campus,Du Cane Rd, London W12 0NN, England
[4] Univ Oxford, Kennedy Inst Rheumatol, Res Grp Tissue & Tumor Microenvironm, Oxford OX3 7LY, England
[5] Max Planck Inst Mol Biomed, Electron Microscopy Unit, D-48149 Munster, Germany
[6] Katholieke Univ Leuven, VIB Vesalius Res Ctr, KU Leuven, B-3000 Leuven, Belgium
[7] Hannover Med Sch, Dept Hypertens & Nephrol, D-30625 Hannover, Germany
[8] Hannover Med Sch, Dept Plast & Reconstruct Surg, D-30625 Hannover, Germany
[9] Univ Edinburgh, MRC Ctr Regenerat Med, Res Grp Ontogeny Haematopoiet Stem Cells, Edinburgh EH16 4UU, Midlothian, Scotland
[10] Univ Torino, Dept Mol Biotechnol & Hlth Sci, Ctr Mol Biotechnol, I-10126 Turin, Italy
来源
NATURE COMMUNICATIONS | 2016年 / 7卷
基金
欧洲研究理事会;
关键词
MOLECULAR REGULATION; ENDOTHELIAL-CELLS; UP-REGULATION; TIP CELLS; NOTCH; ANGIOGENESIS; PATHWAY; VEGF; DLL4; SPECIFICATION;
D O I
10.1038/ncomms13601
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页数:13
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