PUBLICATION
Expression profile of IGF paralog genes in liver and muscle of a GH-transgenic zebrafish
- Authors
- Felix Nornberg, B., Azevedo Figueiredo, M., Fernando Marins, L.
- ID
- ZDB-PUB-160101-5
- Date
- 2016
- Source
- General and comparative endocrinology 226: 36-41 (Journal)
- Registered Authors
- Keywords
- Growth hormone (GH), Insulin-like growth factor (IGF) system, JAK/STAT, MEK/ERK, PI3K/Akt, Transgenic zebrafish
- MeSH Terms
-
- Animals
- Animals, Genetically Modified
- Growth Hormone/genetics
- Growth Hormone/metabolism*
- Liver/metabolism*
- Muscle, Skeletal/metabolism*
- Phosphatidylinositol 3-Kinases/metabolism
- Phosphorylation
- Signal Transduction/genetics
- Somatomedins/genetics
- Somatomedins/metabolism*
- Zebrafish/genetics
- Zebrafish/metabolism*
- PubMed
- 26718079 Full text @ Gen. Comp. Endocrinol.
Citation
Felix Nornberg, B., Azevedo Figueiredo, M., Fernando Marins, L. (2016) Expression profile of IGF paralog genes in liver and muscle of a GH-transgenic zebrafish. General and comparative endocrinology. 226:36-41.
Abstract
The objective of this study was to investigate the relationship between IGFs produced in the liver and skeletal muscle with muscle hypertrophy previously observed in a line of GH-transgenic zebrafish. In this sense, we evaluated the expression of genes related to the IGF system in liver and muscle of transgenics, as well as the main intracellular signaling pathways used by GH/IGF axis. Our results showed an increase in expression of igf1a, igf2a, and igf2b genes in the liver. Moreover, there was a decrease in the expression of igf1ra and an increase in muscle igf2r of transgenics, indicating a negative response of muscle tissue with respect to excess circulating IGFs. Muscle IGFs expression analyses revealed a significant increase only for igf2b, accompanied by a parallel induction of igfbp5a gene. The presence of IGFBP5a may potentiate the IGF2 action in muscle cells differentiation. Regarding JAK/STAT-related genes, we observed an alteration in the expression profile of both stat3 and stat5a in transgenic fish liver. No changes were observed in the muscle, suggesting that both tissues respond differently to GH-transgenesis. Western blotting analyses indicated an imbalance between the phosphorylation levels of the proliferative (MEK/ERK) and hypertrophic (PI3K/Akt) pathways, in favor of the latter. In summary, the results of this study suggest that the hypertrophy caused by GH-transgenesis in zebrafish may be due to circulating IGFs produced by the liver, with an important participation of muscle IGF2b. This group of IGFs appears to be favoring the hypertrophic intracellular pathway in muscle tissue of transgenic zebrafish.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping