Cytoneme-mediated transport of active Wnt5b-Ror2 complexes in zebrafish
dc.contributor.author | Zhang, C | |
dc.contributor.author | Brunt, L | |
dc.contributor.author | Ono, Y | |
dc.contributor.author | Rogers, S | |
dc.contributor.author | Scholpp, S | |
dc.date.accessioned | 2024-01-16T09:59:35Z | |
dc.date.issued | 2023-12-20 | |
dc.date.updated | 2024-01-16T09:04:11Z | |
dc.description.abstract | Chemical signalling is the primary means by which cells communicate in the embryo. The underlying principle refers to a group of ligand-producing cells and a group of cells that respond to this signal because they express the appropriate receptors1,2. In the zebrafish embryo, Wnt5b binds to the receptor Ror2 to trigger the Wnt-planar cell polarity (PCP) signalling pathway to regulate tissue polarity and cell migration3,4. However, it remains unclear how this lipophilic ligand is transported from the source cells through the aqueous extracellular space to the target tissue. In this study, we provide evidence that Wnt5b, together with Ror2, is loaded on long protrusions called cytonemes. Our data further suggest that the active Wnt5b-Ror2 complexes form in the producing cell and are handed over from these cytonemes to the receiving cell. Then, the receiving cell has the capacity to initiate Wnt-PCP signalling, irrespective of its functional Ror2 receptor status. On the tissue level, we further show that cytoneme-dependent spreading of active Wnt5b-Ror2 affects convergence and extension in the zebrafish gastrula. We suggest that cytoneme-mediated transfer of ligand-receptor complexes is a vital mechanism for paracrine signalling. This may prompt a reevaluation of the conventional concept of characterizing responsive and non-responsive tissues solely on the basis of the expression of receptors. | en_GB |
dc.description.sponsorship | Chinese Scholarship Council (CSC) | en_GB |
dc.description.sponsorship | Biotechnology and Biological Sciences Research Council (BBSRC) | en_GB |
dc.description.sponsorship | Living Systems Institute, University of Exeter | en_GB |
dc.description.sponsorship | Medical Research Council (MRC) | en_GB |
dc.format.extent | 126-133 | |
dc.format.medium | Print-Electronic | |
dc.identifier.citation | Vol. 625(7993), pp. 126-133 | en_GB |
dc.identifier.doi | https://doi.org/10.1038/s41586-023-06850-7 | |
dc.identifier.grantnumber | BB/S016295/1 | en_GB |
dc.identifier.grantnumber | BB/X008401/1 | en_GB |
dc.identifier.grantnumber | BB/R013764/1 | en_GB |
dc.identifier.grantnumber | MR/S007970/1 | en_GB |
dc.identifier.uri | http://hdl.handle.net/10871/135033 | |
dc.identifier | ORCID: 0000-0002-7257-0120 (Ono, Yosuke) | |
dc.identifier | ORCID: 0000-0002-4901-4740 (Rogers, Sally) | |
dc.identifier | ORCID: 0000-0002-4903-9657 (Scholpp, Steffen) | |
dc.language.iso | en | en_GB |
dc.publisher | Nature Research | en_GB |
dc.relation.url | https://www.ncbi.nlm.nih.gov/pubmed/38123680 | en_GB |
dc.rights | © The Author(s) 2023. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. | en_GB |
dc.title | Cytoneme-mediated transport of active Wnt5b-Ror2 complexes in zebrafish | en_GB |
dc.type | Article | en_GB |
dc.date.available | 2024-01-16T09:59:35Z | |
dc.contributor.editor | Scholpp, S | |
dc.identifier.issn | 0028-0836 | |
exeter.place-of-publication | England | |
dc.description | This is the final version. Available on open access from Nature Research via the DOI in this record | en_GB |
dc.description | Data availability; Microscopy data reported in this paper and any information required to re-analyse the data reported in this paper are presented within the paper or are available from the corresponding author upon reasonable request. Source data are provided with this paper. | en_GB |
dc.identifier.eissn | 1476-4687 | |
dc.identifier.journal | Nature | en_GB |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | en_GB |
dcterms.dateAccepted | 2023-11-08 | |
rioxxterms.version | VoR | en_GB |
rioxxterms.licenseref.startdate | 2023-12-20 | |
rioxxterms.type | Journal Article/Review | en_GB |
refterms.dateFCD | 2024-01-16T09:55:37Z | |
refterms.versionFCD | VoR | |
refterms.dateFOA | 2024-01-16T10:00:00Z | |
refterms.panel | A | en_GB |
refterms.dateFirstOnline | 2023-12-20 |
Files in this item
This item appears in the following Collection(s)
Except where otherwise noted, this item's licence is described as © The Author(s) 2023. Open Access. This article is licensed under a Creative Commons Attribution
4.0 International License, which permits use, sharing, adaptation, distribution
and reproduction in any medium or format, as long as you give appropriate
credit to the original author(s) and the source, provide a link to the Creative Commons licence,
and indicate if changes were made. The images or other third party material in this article are
included in the article’s Creative Commons licence, unless indicated otherwise in a credit line
to the material. If material is not included in the article’s Creative Commons licence and your
intended use is not permitted by statutory regulation or exceeds the permitted use, you will
need to obtain permission directly from the copyright holder. To view a copy of this licence,
visit http://creativecommons.org/licenses/by/4.0/.