PUBLICATION
Glycogen Synthase Kinase 3 beta in somites plays a role during the angiogenesis of zebrafish embryos
- Authors
- Lee, H.C., Lin, Y.Z., Lai, Y.T., Huang, W.J., Hu, J.R., Tsai, J.N., Tsai, H.J.
- ID
- ZDB-PUB-140728-21
- Date
- 2014
- Source
- The FEBS journal 281(19): 4367-83 (Journal)
- Registered Authors
- Tsai, Huai-Jen
- Keywords
- Angiogenesis, Gsk3b, Somite, Zebrafish, vegf
- MeSH Terms
-
- Animals
- Cleavage Stage, Ovum/enzymology
- Embryo, Nonmammalian/blood supply
- Embryo, Nonmammalian/enzymology
- Endothelium, Vascular/enzymology
- Gene Expression Regulation, Developmental
- Glycogen Synthase Kinase 3/physiology*
- Neovascularization, Physiologic*
- Phosphatidylinositol 3-Kinases/metabolism
- Proto-Oncogene Proteins c-akt/metabolism
- Signal Transduction
- Somites/enzymology*
- Vascular Endothelial Growth Factor A/metabolism
- Wnt Proteins/metabolism
- Zebrafish
- Zebrafish Proteins/physiology*
- PubMed
- 25056693 Full text @ FEBS J.
Citation
Lee, H.C., Lin, Y.Z., Lai, Y.T., Huang, W.J., Hu, J.R., Tsai, J.N., Tsai, H.J. (2014) Glycogen Synthase Kinase 3 beta in somites plays a role during the angiogenesis of zebrafish embryos. The FEBS journal. 281(19):4367-83.
Abstract
Glycogen synthase kinase 3 beta (Gsk3b) acts as a negative modulator in endothelial cells through the Wnt/β-catenin/PI3K/AKT/Gsk3b axis in cancer-induced angiogenesis. However, the function of Gsk3b during embryonic angiogenesis remains unclear. Here, either gsk3b knockdown by morpholino or Gsk3b loss of activity by LiCl treatment had serious phenotypic consequences, such as defects in the positioning and patterning of intersegmental (Se) blood vessels and reduction of vegfaa121 and vegfaa165 transcripts. In embryos treated with the PI3K inhibitor, angiogenesis was severely inhibited, along with reduced Wnt, phosphorylated AKT (pAKT) and phosphorylated Gsk3b (pGsk3b), suggesting that the remaining Gsk3b in somites could still degrade β-catenin, resulting in decreased vegfaa expression. However, in gsk3b-mRNA-overexpressed embryos, Se vessels ectopically sprouted by the increase of pGsk3b which prevented the degradation of β-catenin and promoted the increase of pAKT activity, thus increasing vegfaa expression in somites. Interestingly, the Gsk3b-dependent crosstalk between PI3K/AKT and Wnt/β-catenin suggests that Wnt/β-catenin and PI3K/AKT interaction controls embryonic angiogenesis by a positive feedback loop rather than a hierarchical framework such as that found in cancer-induced angiogenesis. Thus, both active and inactive forms of Gsk3b mediate the cooperative signaling between Wnt/β-catenin and PI3K/AKT to control VegfAa expression in somites during angiogenesis in zebrafish embryos. This article is protected by copyright. All rights reserved.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping