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Tissue-targeted R-spondin mimetics for liver regeneration

R-spondin (RSPO) proteins amplify Wnt signaling and stimulate regeneration in a variety of tissues. To repair tissue in a tissue-specific manner, tissue-targeted RSPO mimetic molecules are desired. Here, we mutated RSPO (RSPO2 F105R/F109A) to eliminate LGR binding while preserving ZNRF3/RNF43 bindin...

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Autores principales: Zhang, Zhengjian, Broderick, Caroline, Nishimoto, Marni, Yamaguchi, Teppei, Lee, Sung-Jin, Zhang, Haili, Chen, Hui, Patel, Mehaben, Ye, Jay, Ponce, Alberto, Brady, Jennifer, Baribault, Hélène, Li, Yang, Yeh, Wen-Chen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7435267/
https://www.ncbi.nlm.nih.gov/pubmed/32811902
http://dx.doi.org/10.1038/s41598-020-70912-3
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author Zhang, Zhengjian
Broderick, Caroline
Nishimoto, Marni
Yamaguchi, Teppei
Lee, Sung-Jin
Zhang, Haili
Chen, Hui
Patel, Mehaben
Ye, Jay
Ponce, Alberto
Brady, Jennifer
Baribault, Hélène
Li, Yang
Yeh, Wen-Chen
author_facet Zhang, Zhengjian
Broderick, Caroline
Nishimoto, Marni
Yamaguchi, Teppei
Lee, Sung-Jin
Zhang, Haili
Chen, Hui
Patel, Mehaben
Ye, Jay
Ponce, Alberto
Brady, Jennifer
Baribault, Hélène
Li, Yang
Yeh, Wen-Chen
author_sort Zhang, Zhengjian
collection PubMed
description R-spondin (RSPO) proteins amplify Wnt signaling and stimulate regeneration in a variety of tissues. To repair tissue in a tissue-specific manner, tissue-targeted RSPO mimetic molecules are desired. Here, we mutated RSPO (RSPO2 F105R/F109A) to eliminate LGR binding while preserving ZNRF3/RNF43 binding and targeted the mutated RSPO to a liver specific receptor, ASGR1. The resulting bi-specific molecule (αASGR1-RSPO2-RA) enhanced Wnt signaling effectively in vitro, and its activity was limited to ASGR1 expressing cells. Systemic administration of αASGR1-RSPO2-RA in mice specifically upregulated Wnt target genes and stimulated cell proliferation in liver but not intestine (which is more responsive to non-targeted RSPO2) in healthy mice, and improved liver function in diseased mice. These results not only suggest that a tissue-specific RSPO mimetic protein can stimulate regeneration in a cell-specific manner, but also provide a blueprint of how a tissue-specific molecule might be constructed for applications in a broader context.
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spelling pubmed-74352672020-08-21 Tissue-targeted R-spondin mimetics for liver regeneration Zhang, Zhengjian Broderick, Caroline Nishimoto, Marni Yamaguchi, Teppei Lee, Sung-Jin Zhang, Haili Chen, Hui Patel, Mehaben Ye, Jay Ponce, Alberto Brady, Jennifer Baribault, Hélène Li, Yang Yeh, Wen-Chen Sci Rep Article R-spondin (RSPO) proteins amplify Wnt signaling and stimulate regeneration in a variety of tissues. To repair tissue in a tissue-specific manner, tissue-targeted RSPO mimetic molecules are desired. Here, we mutated RSPO (RSPO2 F105R/F109A) to eliminate LGR binding while preserving ZNRF3/RNF43 binding and targeted the mutated RSPO to a liver specific receptor, ASGR1. The resulting bi-specific molecule (αASGR1-RSPO2-RA) enhanced Wnt signaling effectively in vitro, and its activity was limited to ASGR1 expressing cells. Systemic administration of αASGR1-RSPO2-RA in mice specifically upregulated Wnt target genes and stimulated cell proliferation in liver but not intestine (which is more responsive to non-targeted RSPO2) in healthy mice, and improved liver function in diseased mice. These results not only suggest that a tissue-specific RSPO mimetic protein can stimulate regeneration in a cell-specific manner, but also provide a blueprint of how a tissue-specific molecule might be constructed for applications in a broader context. Nature Publishing Group UK 2020-08-18 /pmc/articles/PMC7435267/ /pubmed/32811902 http://dx.doi.org/10.1038/s41598-020-70912-3 Text en © The Author(s) 2020 Open AccessThis 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/.
spellingShingle Article
Zhang, Zhengjian
Broderick, Caroline
Nishimoto, Marni
Yamaguchi, Teppei
Lee, Sung-Jin
Zhang, Haili
Chen, Hui
Patel, Mehaben
Ye, Jay
Ponce, Alberto
Brady, Jennifer
Baribault, Hélène
Li, Yang
Yeh, Wen-Chen
Tissue-targeted R-spondin mimetics for liver regeneration
title Tissue-targeted R-spondin mimetics for liver regeneration
title_full Tissue-targeted R-spondin mimetics for liver regeneration
title_fullStr Tissue-targeted R-spondin mimetics for liver regeneration
title_full_unstemmed Tissue-targeted R-spondin mimetics for liver regeneration
title_short Tissue-targeted R-spondin mimetics for liver regeneration
title_sort tissue-targeted r-spondin mimetics for liver regeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7435267/
https://www.ncbi.nlm.nih.gov/pubmed/32811902
http://dx.doi.org/10.1038/s41598-020-70912-3
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