The forming limb skeleton serves as a signaling center for limb vasculature patterning via regulation of Vegf
Author:
Eshkar-Oren Idit1, Viukov Sergey V.1, Salameh Sharbel1, Krief Sharon1, Oh Chun-do2, Akiyama Haruhiko3, Gerber Hans-Peter4, Ferrara Napoleone4, Zelzer Elazar1
Affiliation:
1. Department of Molecular Genetics, Weizmann Institute of Science, Rehovot,Israel. 2. Department of Molecular Genetics, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA. 3. Department of Orthopaedics, Kyoto University, Kyoto 606-8507, Japan. 4. Genentech, 1 DNA Way, S. San Francisco, CA 94080, USA.
Abstract
Limb development constitutes a central model for the study of tissue and organ patterning; yet, the mechanisms that regulate the patterning of limb vasculature have been left understudied. Vascular patterning in the forming limb is tightly regulated in order to ensure sufficient gas exchange and nutrient supply to the developing organ. Once skeletogenesis is initiated,limb vasculature undergoes two seemingly opposing processes: vessel regression from regions that undergo mesenchymal condensation; and vessel morphogenesis. During the latter, vessels that surround the condensations undergo an extensive rearrangement, forming a stereotypical enriched network that is segregated from the skeleton. In this study, we provide evidence for the centrality of the condensing mesenchyme of the forming skeleton in regulating limb vascular patterning. Both Vegf loss- and gain-of-function experiments in limb bud mesenchyme firmly established VEGF as the signal by which the condensing mesenchyme regulates the vasculature. Normal vasculature observed in limbs where VEGF receptors Flt1, Flk1, Nrp1 and Nrp2 were blocked in limb bud mesenchyme suggested that VEGF, which is secreted by the condensing mesenchyme, regulates limb vasculature via a direct long-range mechanism. Finally, we provide evidence for the involvement of SOX9 in the regulation of Vegf expression in the condensing mesenchyme. This study establishes Vegf expression in the condensing mesenchyme as the mechanism by which the skeleton patterns limb vasculature.
Publisher
The Company of Biologists
Subject
Developmental Biology,Molecular Biology
Reference75 articles.
1. Akiyama, H., Chaboissier, M. C., Martin, J. F., Schedl, A. and de Crombrugghe, B. (2002). The transcription factor Sox9 has essential roles in successive steps of the chondrocyte differentiation pathway and is required for expression of Sox5 and Sox6. Genes Dev.16,2813-2828. 2. Akiyama, H., Kim, J. E., Nakashima, K., Balmes, G., Iwai, N.,Deng, J. M., Zhang, Z., Martin, J. F., Behringer, R. R., Nakamura, T. et al. (2005). Osteo-chondroprogenitor cells are derived from Sox9 expressing precursors. Proc. Natl. Acad. Sci. USA102,14665-14670. 3. Akiyama, H., Stadler, H. S., Martin, J. F., Ishii, T. M.,Beachy, P. A., Nakamura, T. and de Crombrugghe, B. (2007). Misexpression of Sox9 in mouse limb bud mesenchyme induces polydactyly and rescues hypodactyly mice. Matrix Biol.26,224-233. 4. Amarilio, R., Viukov, S. V., Sharir, A., Eshkar-Oren, I.,Johnson, R. S. and Zelzer, E. (2007). HIF1alpha regulation of Sox9 is necessary to maintain differentiation of hypoxic prechondrogenic cells during early skeletogenesis. Development134,3917-3928. 5. Ambler, C. A., Nowicki, J. L., Burke, A. C. and Bautch, V. L. (2001). Assembly of trunk and limb blood vessels involves extensive migration and vasculogenesis of somite-derived angioblasts. Dev. Biol.234,352-364.
Cited by
97 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|