Trpv5/6 is vital for epithelial calcium uptake and bone formation
- Authors
- Vanoevelen, J., Janssens, A., Huitema, L.F., Hammond, C.L., Metz, J.R., Flik, G., Voets, T., and Schulte-Merker, S.
- ID
- ZDB-PUB-110628-15
- Date
- 2011
- Source
- FASEB journal : official publication of the Federation of American Societies for Experimental Biology 25(9): 3197-207 (Journal)
- Registered Authors
- Flik, Gert, Huitema, Leonie, Metz, Juriaan R., Schulte-Merker, Stefan
- Keywords
- zebrafish, osetogenesis
- MeSH Terms
-
- Animals
- Bone Development/genetics
- Bone Development/physiology*
- Calcium/metabolism*
- Embryo, Nonmammalian/metabolism
- Epithelium/embryology*
- Epithelium/metabolism*
- Gene Expression Regulation, Developmental/physiology
- HEK293 Cells
- Humans
- Molecular Sequence Data
- Mutation
- TRPV Cation Channels/genetics
- TRPV Cation Channels/metabolism*
- Zebrafish/embryology*
- Zebrafish Proteins/genetics
- Zebrafish Proteins/metabolism*
- PubMed
- 21670068 Full text @ FASEB J.
Calcium is an essential ion serving a multitude of physiological roles. Aside from its role as a second messenger, it is an essential component of the vertebrate bone matrix. Efficient uptake and storage of calcium are therefore indispensable for all vertebrates. Transient receptor potential family, vanilloid type (TRPV)5 and TRPV6 channels are known players in transcellular calcium uptake, but the exact contribution of this pathway is unclear. We used forward genetic screening in zebrafish (Danio rerio) to identify genes essential in bone formation and identified a lethal zebrafish mutant (matt-und-schlapp) with severe defects in bone formation, including lack of ossification of the vertebral column and craniofacial structures. Mutant embryos show a 68% reduction in calcium content, and systemic calcium homeostasis is disturbed when compared with siblings. The phenotype can be partially rescued by increasing ambient calcium levels to 25 mM. We identified the mutation as a loss-of-function mutation in the single orthologue of TRPV5 and 6, trpv5/6. Expression in HEK293 cells showed that Trpv5/6 is a calcium-selective channel capable of inward calcium transport at physiological concentrations whereas the mutant channel is not. Taken together, this study provides both genetic and functional evidence that transcellular epithelial calcium uptake is vital to sustain life and enable bone formation.