Copyright © 2004, European Society of Cardiology
Control of arterial branching morphogenesis in embryogenesis: go with the flow
aCollège de France, Laboratoire de Médecine Expérimentale, Inserm U36, 11 Place Marcelin Berthelot Paris 75231, France
bDepartment of Physiology, Cardiovascular Research Institute Maastricht (CARIM), P.O.B616 6200MD, Maastricht, The Netherlands
cLaboratoire de Physique de la Matière Condensé, Ecole Polytechnique 91128, Palaiseau, France
dInstitute of Physiology, CBF, Charité Berlin, Arnimallee 22, 14195 Berlin, Germany
* Corresponding author. Department of Physiology, Cardiovascular Research Institute Maastricht, Maastricht University, P.O.B 616, 6200MD, Maastricht, The Netherlands. Tel.: +31 43 3881084/1200; fax: +31 43 3884166. Email address: lenoble{at}fys.unimaas.nl
Formation of a properly branched vascular system during embryogenesis is crucial for embryo survival. Here we review the regulation of the morphogenesis of the arterial and venous system during embryogenesis. We show that in addition to deterministic patterning mechanisms and plasticity of endothelial cells, arterial-venous differentiation and branching morphogenesis involves a prominent role for blood flow. Based on in vivo observations of developing arteries, we identified a novel morphological event crucial for the morphogenesis of the arterial tree, disconnection of small side branches. This disconnection of side branches occurs exactly at the point of bifurcation. The rate of disconnection of side branches depends on flow velocity and branching angle. The balance between disconnection and maintenance of arterial side branches determines the number of side branches connected to a large artery. Based on these observations, we postulate that the number of pre-existing collaterals connected to a large artery is a function of the disconnection process and can be regulated by hemodynamics. We furthermore show that embryonic arteries already adapt their lumen diameter to the amount of flow carried. Taken together, we suggest that hemodynamics plays a pivotal role in shaping the arterial system. We suggest that flow-evoked remodeling processes determine the number of preexisting collaterals during critical periods of embryo–fetal development. Insight into these basic principles of arterial growth and branching during embryogenesis may aid to understanding the observed variability in the capacity to establish a collateral circulation in patients with ischemic diseases and finding new strategies for therapeutic arteriogenesis.
KEYWORDS Developmental biology; Arterial–venous differentiation; Arteriogenesis; Endothelial receptors; Hemodynamics; Growth factors
* Mark Post and Johannes Waltenberger acted as guest editors for this article.
Time for primary review 29 days
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
M. A. Schwarz, L. Caldwell, D. Cafasso, and H. Zheng Emerging pulmonary vasculature lacks fate specification Am J Physiol Lung Cell Mol Physiol, January 1, 2009; 296(1): L71 - L81. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Horowitz and M. Simons Branching Morphogenesis Circ. Res., October 10, 2008; 103(8): 784 - 795. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. le Noble, C. Klein, A. Tintu, A. Pries, and I. Buschmann Neural guidance molecules, tip cells, and mechanical factors in vascular development Cardiovasc Res, May 1, 2008; 78(2): 232 - 241. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. J. Hofmann and M. L. Iruela-Arispe Notch Signaling in Blood Vessels: Who Is Talking to Whom About What? Circ. Res., June 8, 2007; 100(11): 1556 - 1568. [Abstract] [Full Text] [PDF] |
||||
![]() |
O. Dumont, L. Loufrani, and D. Henrion Key Role of the NO-Pathway and Matrix Metalloprotease-9 in High Blood Flow-Induced Remodeling of Rat Resistance Arteries Arterioscler Thromb Vasc Biol, February 1, 2007; 27(2): 317 - 324. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. A. V. Jones, F. le Noble, and A. Eichmann What Determines Blood Vessel Structure? Genetic Prespecification vs. Hemodynamics. Physiology, December 1, 2006; 21(6): 388 - 395. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Murakami, K. Suzuma, H. Takagi, M. Kita, H. Ohashi, D. Watanabe, T. Ojima, M. Kurimoto, T. Kimura, A. Sakamoto, et al. Time-Lapse Imaging of Vitreoretinal Angiogenesis Originating from Both Quiescent and Mature Vessels in a Novel Ex Vivo System Invest. Ophthalmol. Vis. Sci., December 1, 2006; 47(12): 5529 - 5536. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Labat, R. S. A. Cunha, P. Challande, M. E. Safar, and P. Lacolley Respective contribution of age, mean arterial pressure, and body weight on central arterial distensibility in SHR Am J Physiol Heart Circ Physiol, April 1, 2006; 290(4): H1534 - H1539. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Yu, E. D. deMuinck, Z. Zhuang, M. Drinane, K. Kauser, G. M. Rubanyi, H. S. Qian, T. Murata, B. Escalante, and W. C. Sessa Endothelial nitric oxide synthase is critical for ischemic remodeling, mural cell recruitment, and blood flow reserve PNAS, August 2, 2005; 102(31): 10999 - 11004. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Post and J. Waltenberger Modulation of growth factor action in the cardiovascular system Cardiovasc Res, February 15, 2005; 65(3): 547 - 549. [Full Text] [PDF] |
||||







