Assessment of Frizzled 6 membrane mobility by FRAP supports G protein coupling and reveals WNT-Frizzled selectivity
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
24873871
DOI
10.1016/j.cellsig.2014.05.012
PII: S0898-6568(14)00182-X
Knihovny.cz E-resources
- Keywords
- Class Frizzled, Fluorescence recovery after photobleaching, GPCRs, Heterotrimeric G proteins, WNT signaling,
- MeSH
- Cell Membrane metabolism MeSH
- Ethylmaleimide pharmacology MeSH
- Fluorescence Recovery After Photobleaching * MeSH
- Frizzled Receptors agonists genetics metabolism MeSH
- HEK293 Cells MeSH
- Heterotrimeric GTP-Binding Proteins metabolism MeSH
- Humans MeSH
- Pertussis Toxin toxicity MeSH
- Wnt-5a Protein MeSH
- GTP-Binding Protein alpha Subunits, Gi-Go metabolism MeSH
- Wnt Proteins genetics metabolism MeSH
- Proto-Oncogene Proteins genetics metabolism MeSH
- Recombinant Proteins genetics metabolism MeSH
- Signal Transduction drug effects MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Ethylmaleimide MeSH
- Frizzled Receptors MeSH
- FZD6 protein, human MeSH Browser
- Heterotrimeric GTP-Binding Proteins MeSH
- Pertussis Toxin MeSH
- Wnt-5a Protein MeSH
- GTP-Binding Protein alpha Subunits, Gi-Go MeSH
- Wnt Proteins MeSH
- Proto-Oncogene Proteins MeSH
- Recombinant Proteins MeSH
- WNT5A protein, human MeSH Browser
The WNT receptors of the Frizzled family comprise ten mammalian isoforms, bind WNT proteins and mediate downstream signaling to regulate stem cell fate, neuronal differentiation, cell survival and more. WNT-induced signaling pathways are either β-catenin-dependent or -independent, thereby dividing the 19 mammalian WNT proteins into two groups. So far hardly any quantitative, pharmacological information is available about WNT-FZD interaction profiles, affinities or mechanisms of signaling specification through distinct WNT/FZD pairings. This lack of knowledge originates from difficulties with WNT purification and a lack of suitable assays, such as ligand binding assays and FZD activity readouts. In order to minimize this gap, we employ fluorescence recovery after photobleaching (FRAP) to investigate WNT effects on the lateral mobility of FZD6-GFP in living cells. Pharmacological uncoupling of heterotrimeric G proteins by pertussis toxin and N-ethylmaleimide argues that changes in FZD6 mobility are related to putative precoupling of heterotrimeric Gi/o proteins to FZD6. We show that recombinant WNT-1, -2, 3A, -4, -5A, -7A, -9B and -10B affect FZD6 surface mobility and thus act on this receptor. WNT-5B and WNT-11, on the other hand, have no effect on FZD6 mobility and we conclude that they do not act through FZD6. We introduce here a novel way to assess WNT-FZD interaction by live cell imaging allowing further mapping of WNT-FZD interactions and challenging previous experimental limitations. Increased understanding of WNT-FZD selectivity provides important insight into the biological function of this crucial signaling system with importance in developmental biology, stem cell regulation oncogenesis, and human disease.
References provided by Crossref.org
WNT5B in Physiology and Disease
Agonist-induced dimer dissociation as a macromolecular step in G protein-coupled receptor signaling
WNT Stimulation Dissociates a Frizzled 4 Inactive-State Complex with Gα12/13