Sclerostin Binds to LRP5/6 and Antagonizes Canonical Wnt Signaling
UConn Health · University of Missouri–Kansas City · +1 more institution
Abstract
The loss of the SOST gene product sclerostin leads to sclerosteosis characterized by high bone mass. In this report, we found that sclerostin could antagonize canonical Wnt signaling in human embryonic kidney A293T cells and mouse osteoblastic MC3T3 cells. This sclerostin-mediated antagonism could be reversed by overexpression of Wnt co-receptor low density lipoprotein receptor-related protein (LRP) 5. In addition, we found that sclerostin bound to LRP5 as well as LRP6 and identified the first two YWTD-EGF repeat domains of LRP5 as being responsible for the binding. Although these two repeat domains are required for transduction of canonical Wnt signals, canonical Wnt did not appear to compete with sclerostin…
Citation impact
- FWCI
- 16.68
- Percentile
- 100%
- References
- 40
Authors
8Topics & keywords
- Sclerostin
- Wnt signaling pathway
- LRP5
- Cell biology
- LRP6
- Chemistry
- Internal medicine
- Biology