PUBLICATION
Tmem2 Regulates Embryonic Vegf Signaling by Controlling Hyaluronic Acid Turnover
- Authors
- De Angelis, J.E., Lagendijk, A.K., Chen, H., Tromp, A., Bower, N.I., Tunny, K.A., Brooks, A.J., Bakkers, J., Francois, M., Yap, A.S., Simons, C., Wicking, C., Hogan, B.M., Smith, K.A.
- ID
- ZDB-PUB-170125-2
- Date
- 2017
- Source
- Developmental Cell 40: 123-136 (Journal)
- Registered Authors
- Bakkers, Jeroen, Hogan, Ben M., Smith, Kelly
- Keywords
- VEGF, angiogenesis, extracellular matrix, hyaluronic acid, tmem2, zebrafish
- MeSH Terms
-
- Embryo, Nonmammalian/metabolism*
- Signal Transduction*
- Mutation/genetics
- Zebrafish Proteins/chemistry
- Zebrafish Proteins/metabolism*
- Endothelial Cells/metabolism
- Animals
- Neovascularization, Physiologic
- Polymerization
- Hyaluronic Acid/metabolism*
- Membrane Proteins/chemistry
- Membrane Proteins/metabolism*
- Vascular Endothelial Growth Factor A/metabolism*
- Zebrafish/embryology*
- Zebrafish/metabolism*
- Arteries/metabolism
- Phenotype
- Torso/blood supply
- Veins/metabolism
- PubMed
- 28118600 Full text @ Dev. Cell
Citation
De Angelis, J.E., Lagendijk, A.K., Chen, H., Tromp, A., Bower, N.I., Tunny, K.A., Brooks, A.J., Bakkers, J., Francois, M., Yap, A.S., Simons, C., Wicking, C., Hogan, B.M., Smith, K.A. (2017) Tmem2 Regulates Embryonic Vegf Signaling by Controlling Hyaluronic Acid Turnover. Developmental Cell. 40:123-136.
Abstract
Angiogenesis is responsible for tissue vascularization during development, as well as in pathological contexts, including cancer and ischemia. Vascular endothelial growth factors (VEGFs) regulate angiogenesis by acting through VEGF receptors to induce endothelial cell signaling. VEGF is processed in the extracellular matrix (ECM), but the complexity of ECM control of VEGF signaling and angiogenesis remains far from understood. In a forward genetic screen, we identified angiogenesis defects in tmem2 zebrafish mutants that lack both arterial and venous Vegf/Vegfr/Erk signaling. Strikingly, tmem2 mutants display increased hyaluronic acid (HA) surrounding developing vessels. Angiogenesis in tmem2 mutants was rescued, or restored after failed sprouting, by degrading this increased HA. Furthermore, oligomerized HA or overexpression of Vegfc rescued angiogenesis in tmem2 mutants. Based on these data, and the known structure of Tmem2, we find that Tmem2 regulates HA turnover to promote normal Vegf signaling during developmental angiogenesis.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping