Brag2 differentially regulates β1- and β3-integrin-dependent adhesion in endothelial cells and is involved in developmental and pathological angiogenesis
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- 作者：Yosif Manavski (2)
Guillaume Carmona (2) (7)
Katrin Bennewitz (3)
Zhongshu Tang (4)
Fan Zhang (5)
Atsuko Sakurai (6)
Andreas M. Zeiher (1)
J. Silvio Gutkind (6)
Xuri Li (4)
Jens Kroll (3) (8)
Stefanie Dimmeler (2)
Emmanouil Chavakis (1) (2) - 关键词：Angiogenesis ; Brag2 ; Endocytosis ; Integrins ; Migration
- 刊名：Basic Research in Cardiology
- 出版年：2014
- 出版时间：March 2014
- 年：2014
- 卷：109
- 期：2
- 全文大小：5,125 KB
- 作者单位：Yosif Manavski (2)
Guillaume Carmona (2) (7)
Katrin Bennewitz (3)
Zhongshu Tang (4)
Fan Zhang (5)
Atsuko Sakurai (6)
Andreas M. Zeiher (1)
J. Silvio Gutkind (6)
Xuri Li (4)
Jens Kroll (3) (8)
Stefanie Dimmeler (2)
Emmanouil Chavakis (1) (2)
2. Institute of Cardiovascular Regeneration, Goethe University Frankfurt, Frankfurt, Germany
7. David H Koch Institute for Integrative Cancer Research at Massachusetts Institute of Technology, Cambridge, MA, 02139-4307, USA
3. Department of Vascular Biology and Tumor Angiogenesis, Center for Biomedicine and Medical Technology Mannheim (CBTM), Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany
4. State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-Sen University, Guangzhou, 510060, People’s Republic of China
5. NEI, National Institutes of Health, Bethesda, MD, USA
6. Oral and Pharyngeal Cancer Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA
1. Department of Internal Medicine III, Cardiology, Goethe University of Frankfurt, Theodor-Stern-Kai 7, 60590, Frankfurt, Germany
8. Division of Vascular Oncology and Metastasis, German Cancer Research Center (DKFZ-ZMBH Alliance), Heidelberg, Germany - ISSN：1435-1803
文摘
β1-Integrins are essential for angiogenesis. The mechanisms regulating integrin function in endothelial cells (EC) and their contribution to angiogenesis remain elusive. Brag2 is a guanine nucleotide exchange factor for the small Arf-GTPases Arf5 and Arf6. The role of Brag2 in EC and angiogenesis and the underlying molecular mechanisms remain unclear. siRNA-mediated Brag2-silencing reduced EC angiogenic sprouting and migration. Brag2-siRNA transfection differentially affected α5β1- and αVβ3-integrin function: specifically, Brag2-silencing increased focal/fibrillar adhesions and adhesion on β1-integrin ligands (fibronectin and collagen), while reducing the adhesion on the αVβ3-integrin ligand, vitronectin. Consistent with these results, Brag2-silencing enhanced surface expression of α5β1-integrin, while reducing surface expression of αVβ3-integrin. Mechanistically, Brag2-mediated αVβ3-integrin-recycling and β1-integrin endocytosis and specifically of the active/matrix-bound α5β1-integrin present in fibrillar/focal adhesions (FA), suggesting that Brag2 contributes to the disassembly of FA via β1-integrin endocytosis. Arf5 and Arf6 are promoting downstream of Brag2 angiogenic sprouting, β1-integrin endocytosis and the regulation of FA. In vivo silencing of the Brag2-orthologues in zebrafish embryos using morpholinos perturbed vascular development. Furthermore, in vivo intravitreal injection of plasmids containing Brag2-shRNA reduced pathological ischemia-induced retinal and choroidal neovascularization. These data reveal that Brag2 is essential for developmental and pathological angiogenesis by promoting EC sprouting through regulation of adhesion by mediating β1-integrin internalization and link for the first time the process of β1-integrin endocytosis with angiogenesis.