PUBLICATION
Hematopoietic growth factors: the scenario in zebrafish
- Authors
- Pazhakh, V., Lieschke, G.J.
- ID
- ZDB-PUB-190216-2
- Date
- 2019
- Source
- Growth factors (Chur, Switzerland) 36(5-6): 196-212 (Review)
- Registered Authors
- Lieschke, Graham J., Pazhakh, Vahid
- Keywords
- Hematopoiesis, colony-stimulating factor, cytokine, growth factor, interleukin, zebrafish
- MeSH Terms
-
- Animals
- Hematopoiesis*
- Intercellular Signaling Peptides and Proteins/metabolism*
- Signal Transduction
- Zebrafish
- Zebrafish Proteins/metabolism*
- PubMed
- 30764671 Full text @ Growth Factors
Citation
Pazhakh, V., Lieschke, G.J. (2019) Hematopoietic growth factors: the scenario in zebrafish. Growth factors (Chur, Switzerland). 36(5-6):196-212.
Abstract
Humoral regulation by ligand/receptor interactions is a fundamental feature of vertebrate hematopoiesis. Zebrafish are an established vertebrate animal model of hematopoiesis, sharing with mammals conserved genetic, molecular and cell biological regulatory mechanisms. This comprehensive review considers zebrafish hematopoiesis from the perspective of the hematopoietic growth factors (HGFs), their receptors and their actions. Zebrafish possess multiple HGFs: CSF1 (M-CSF) and CSF3 (G-CSF), kit ligand (KL, SCF), erythropoietin (EPO), thrombopoietin (THPO/TPO), and the interleukins IL6, IL11, and IL34. Some ligands and/or receptor components have been duplicated by various mechanisms including the teleost whole genome duplication, adding complexity to the ligand/receptor interactions possible, but also providing examples of several different outcomes of ligand and receptor subfunctionalization or neofunctionalization. CSF2 (GM-CSF), IL3 and IL5 and their receptors are absent from zebrafish. Overall the humoral regulation of hematopoiesis in zebrafish displays considerable similarity with mammals, which can be applied in biological and disease modelling research.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping