Midkine-b regulates cell specification at the neural plate border in zebrafish
- Liedtke, D., and Winkler, C.
- Developmental Dynamics : an official publication of the American Association of Anatomists 237(1): 62-74 (Journal)
- Registered Authors
- Liedtke, Daniel, Winkler, Christoph
- neural crest, sensory neurons, heparin-binding growth factors, midkine, pleiotrophin, zebrafish
- MeSH Terms
- Gene Expression Regulation, Developmental/drug effects
- In Situ Hybridization
- Lithium Chloride/pharmacology
- Neural Crest/drug effects
- Neural Crest/embryology
- Neural Crest/metabolism*
- Neurons, Afferent/cytology
- Neurons, Afferent/drug effects
- Neurons, Afferent/metabolism
- Zebrafish Proteins/genetics*
- Zebrafish Proteins/metabolism
- p-Aminoazobenzene/analogs & derivatives
- 18058915 Full text @ Dev. Dyn.
Liedtke, D., and Winkler, C. (2008) Midkine-b regulates cell specification at the neural plate border in zebrafish. Developmental Dynamics : an official publication of the American Association of Anatomists. 237(1):62-74.
Midkines compose a family of secreted, heparin-binding growth factors with neurotrophic activity in vitro, but largely unknown functions in mammals in vivo. Here we show that one member of this family, Midkine-b (Mdkb), is responsible for establishment of the neural plate border in zebrafish. We propose that MdkB acts downstream of several signaling factors, most notably retinoic acid, implicated in neural crest cell (ncc) induction and refines a zone of competence for ncc and Rohon-Beard (RB) sensory neuron formation. Overexpression of Mdkb expands the cell numbers of various ncc precursor subtypes and results in a significant increase in the number of RB neurons at the neural plate border. On the other hand, Morpholino-mediated knockdown of Mdkb leads to a dramatic reduction of ncc and a loss of sensory neurons. Our results imply that Mdkb is required for the earliest steps of cell specification at the neural plate border in zebrafish.
Genes / Markers
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Engineered Foreign Genes