PUBLICATION
The PDZ Protein Na+/H+ Exchanger Regulatory Factor-1 (NHERF1) Regulates Planar Cell Polarity and Motile Cilia Organization
- Authors
- Treat, A.C., Wheeler, D.S., Stolz, D.B., Tsang, M., Friedman, P.A., Romero, G.
- ID
- ZDB-PUB-160408-1
- Date
- 2016
- Source
- PLoS One 11(4): e0153144 (Journal)
- Registered Authors
- Tsang, Michael
- Keywords
- Cilia, Hydrocephalus, Cell membranes, Embryos, Immunoprecipitation, Tetracyclines, Zebrafish, Wnt signaling cascade
- MeSH Terms
-
- Animals
- CHO Cells
- Cell Polarity
- Cilia/physiology
- Cilia/ultrastructure*
- Cricetulus
- Gene Knockdown Techniques
- Hydrocephalus/genetics*
- Hydrocephalus/veterinary
- Mice
- Phosphoproteins/chemistry
- Phosphoproteins/genetics*
- Phosphoproteins/metabolism*
- Sodium-Hydrogen Exchangers/chemistry
- Sodium-Hydrogen Exchangers/genetics*
- Sodium-Hydrogen Exchangers/metabolism*
- Wnt Signaling Pathway
- Zebrafish
- PubMed
- 27055101 Full text @ PLoS One
Citation
Treat, A.C., Wheeler, D.S., Stolz, D.B., Tsang, M., Friedman, P.A., Romero, G. (2016) The PDZ Protein Na+/H+ Exchanger Regulatory Factor-1 (NHERF1) Regulates Planar Cell Polarity and Motile Cilia Organization. PLoS One. 11(4):e0153144.
Abstract
Directional flow of the cerebrospinal fluid requires coordinated movement of the motile cilia of the ependymal epithelium that lines the cerebral ventricles. Here we report that mice lacking the Na+/H+ Exchanger Regulatory Factor 1 (NHERF1/Slc9a3r1, also known as EBP50) develop profound communicating hydrocephalus associated with fewer and disorganized ependymal cilia. Knockdown of NHERF1/slc9a3r1 in zebrafish embryos also causes severe hydrocephalus of the hindbrain and impaired ciliogenesis in the otic vesicle. Ultrastructural analysis did not reveal defects in the shape or organization of individual cilia. Similar phenotypes have been described in animals with deficiencies in Wnt signaling and the Planar Cell Polarity (PCP) pathway. We show that NHERF1 binds the PCP core genes Frizzled (Fzd) and Vangl. We further show that NHERF1 assembles a ternary complex with Fzd4 and Vangl2 and promotes translocation of Vangl2 to the plasma membrane, in particular to the apical surface of ependymal cells. Taken together, these results strongly support an important role for NHERF1 in the regulation of PCP signaling and the development of functional motile cilia.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping