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R-spondins engage heparan sulfate proteoglycans to potentiate WNT signaling
R-spondins (RSPOs) amplify WNT signaling during development and regenerative responses. We previously demonstrated that RSPOs 2 and 3 potentiate WNT/β-catenin signaling in cells lacking leucine-rich repeat-containing G-protein coupled receptors (LGRs) 4, 5 and 6 (Lebensohn and Rohatgi, 2018). We now...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7239654/ https://www.ncbi.nlm.nih.gov/pubmed/32432544 http://dx.doi.org/10.7554/eLife.54469 |
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author | Dubey, Ramin van Kerkhof, Peter Jordens, Ingrid Malinauskas, Tomas Pusapati, Ganesh V McKenna, Joseph K Li, Dan Carette, Jan E Ho, Mitchell Siebold, Christian Maurice, Madelon Lebensohn, Andres M Rohatgi, Rajat |
author_facet | Dubey, Ramin van Kerkhof, Peter Jordens, Ingrid Malinauskas, Tomas Pusapati, Ganesh V McKenna, Joseph K Li, Dan Carette, Jan E Ho, Mitchell Siebold, Christian Maurice, Madelon Lebensohn, Andres M Rohatgi, Rajat |
author_sort | Dubey, Ramin |
collection | PubMed |
description | R-spondins (RSPOs) amplify WNT signaling during development and regenerative responses. We previously demonstrated that RSPOs 2 and 3 potentiate WNT/β-catenin signaling in cells lacking leucine-rich repeat-containing G-protein coupled receptors (LGRs) 4, 5 and 6 (Lebensohn and Rohatgi, 2018). We now show that heparan sulfate proteoglycans (HSPGs) act as alternative co-receptors for RSPO3 using a combination of ligand mutagenesis and ligand engineering. Mutations in RSPO3 residues predicted to contact HSPGs impair its signaling capacity. Conversely, the HSPG-binding domains of RSPO3 can be entirely replaced with an antibody that recognizes heparan sulfate (HS) chains attached to multiple HSPGs without diminishing WNT-potentiating activity in cultured cells and intestinal organoids. A genome-wide screen for mediators of RSPO3 signaling in cells lacking LGRs 4, 5 and 6 failed to reveal other receptors. We conclude that HSPGs are RSPO co-receptors that potentiate WNT signaling in the presence and absence of LGRs. |
format | Online Article Text |
id | pubmed-7239654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-72396542020-05-22 R-spondins engage heparan sulfate proteoglycans to potentiate WNT signaling Dubey, Ramin van Kerkhof, Peter Jordens, Ingrid Malinauskas, Tomas Pusapati, Ganesh V McKenna, Joseph K Li, Dan Carette, Jan E Ho, Mitchell Siebold, Christian Maurice, Madelon Lebensohn, Andres M Rohatgi, Rajat eLife Cell Biology R-spondins (RSPOs) amplify WNT signaling during development and regenerative responses. We previously demonstrated that RSPOs 2 and 3 potentiate WNT/β-catenin signaling in cells lacking leucine-rich repeat-containing G-protein coupled receptors (LGRs) 4, 5 and 6 (Lebensohn and Rohatgi, 2018). We now show that heparan sulfate proteoglycans (HSPGs) act as alternative co-receptors for RSPO3 using a combination of ligand mutagenesis and ligand engineering. Mutations in RSPO3 residues predicted to contact HSPGs impair its signaling capacity. Conversely, the HSPG-binding domains of RSPO3 can be entirely replaced with an antibody that recognizes heparan sulfate (HS) chains attached to multiple HSPGs without diminishing WNT-potentiating activity in cultured cells and intestinal organoids. A genome-wide screen for mediators of RSPO3 signaling in cells lacking LGRs 4, 5 and 6 failed to reveal other receptors. We conclude that HSPGs are RSPO co-receptors that potentiate WNT signaling in the presence and absence of LGRs. eLife Sciences Publications, Ltd 2020-05-20 /pmc/articles/PMC7239654/ /pubmed/32432544 http://dx.doi.org/10.7554/eLife.54469 Text en http://creativecommons.org/publicdomain/zero/1.0/ http://creativecommons.org/publicdomain/zero/1.0/This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (http://creativecommons.org/publicdomain/zero/1.0/) . |
spellingShingle | Cell Biology Dubey, Ramin van Kerkhof, Peter Jordens, Ingrid Malinauskas, Tomas Pusapati, Ganesh V McKenna, Joseph K Li, Dan Carette, Jan E Ho, Mitchell Siebold, Christian Maurice, Madelon Lebensohn, Andres M Rohatgi, Rajat R-spondins engage heparan sulfate proteoglycans to potentiate WNT signaling |
title | R-spondins engage heparan sulfate proteoglycans to potentiate WNT signaling |
title_full | R-spondins engage heparan sulfate proteoglycans to potentiate WNT signaling |
title_fullStr | R-spondins engage heparan sulfate proteoglycans to potentiate WNT signaling |
title_full_unstemmed | R-spondins engage heparan sulfate proteoglycans to potentiate WNT signaling |
title_short | R-spondins engage heparan sulfate proteoglycans to potentiate WNT signaling |
title_sort | r-spondins engage heparan sulfate proteoglycans to potentiate wnt signaling |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7239654/ https://www.ncbi.nlm.nih.gov/pubmed/32432544 http://dx.doi.org/10.7554/eLife.54469 |
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