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Ecrg4 peptide is the ligand of multiple scavenger receptors

Esophageal cancer-related gene 4 (Ecrg4) encodes a hormone-like peptide that is believed to be involved in a variety of physiological phenomena, including tumour suppression. Recent progress in the study of Ecrg4 has shown that Ecrg4 is a proinflammatory factor and induces the expression of several...

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Autores principales: Moriguchi, Tetsuo, Takeda, Shuji, Iwashita, Shinzo, Enomoto, Kei, Sawamura, Tatsuya, Koshimizu, Uichi, Kondo, Toru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840397/
https://www.ncbi.nlm.nih.gov/pubmed/29511297
http://dx.doi.org/10.1038/s41598-018-22440-4
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author Moriguchi, Tetsuo
Takeda, Shuji
Iwashita, Shinzo
Enomoto, Kei
Sawamura, Tatsuya
Koshimizu, Uichi
Kondo, Toru
author_facet Moriguchi, Tetsuo
Takeda, Shuji
Iwashita, Shinzo
Enomoto, Kei
Sawamura, Tatsuya
Koshimizu, Uichi
Kondo, Toru
author_sort Moriguchi, Tetsuo
collection PubMed
description Esophageal cancer-related gene 4 (Ecrg4) encodes a hormone-like peptide that is believed to be involved in a variety of physiological phenomena, including tumour suppression. Recent progress in the study of Ecrg4 has shown that Ecrg4 is a proinflammatory factor and induces the expression of several cytokines and chemokines in macrophages/microglia. However, the detailed molecular mechanisms of Ecrg4 signalling, especially the Ecrg4 receptors, remain poorly understood. Here, using retrovirus-mediated expression cloning, we identified lectin-like oxidised low-density lipoprotein receptor-1 (LOX-1) as a membrane protein that binds amino acid residues 71–132 of Ecrg4 (Ecrg4(71–132)). Moreover, in addition to LOX-1, several scavenger receptors, such as Scarf1, Cd36 and Stabilin-1, facilitated the efficient internalisation of Ecrg4(71–132) into cells. A broad competitive inhibitor of scavenger receptors, polyinosinic acid, reduced both the binding of Ecrg4(71–132) and the activation of NF-κB in microglia. This activation was dependent on MyD88, an adaptor protein that recruits signalling proteins to Toll-like receptors (TLRs), with the consequent induction of various immune responses. These data suggest that multiple scavenger receptors recognise Ecrg4(71–132) and transduce its signals, together with TLRs, in microglia.
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spelling pubmed-58403972018-03-13 Ecrg4 peptide is the ligand of multiple scavenger receptors Moriguchi, Tetsuo Takeda, Shuji Iwashita, Shinzo Enomoto, Kei Sawamura, Tatsuya Koshimizu, Uichi Kondo, Toru Sci Rep Article Esophageal cancer-related gene 4 (Ecrg4) encodes a hormone-like peptide that is believed to be involved in a variety of physiological phenomena, including tumour suppression. Recent progress in the study of Ecrg4 has shown that Ecrg4 is a proinflammatory factor and induces the expression of several cytokines and chemokines in macrophages/microglia. However, the detailed molecular mechanisms of Ecrg4 signalling, especially the Ecrg4 receptors, remain poorly understood. Here, using retrovirus-mediated expression cloning, we identified lectin-like oxidised low-density lipoprotein receptor-1 (LOX-1) as a membrane protein that binds amino acid residues 71–132 of Ecrg4 (Ecrg4(71–132)). Moreover, in addition to LOX-1, several scavenger receptors, such as Scarf1, Cd36 and Stabilin-1, facilitated the efficient internalisation of Ecrg4(71–132) into cells. A broad competitive inhibitor of scavenger receptors, polyinosinic acid, reduced both the binding of Ecrg4(71–132) and the activation of NF-κB in microglia. This activation was dependent on MyD88, an adaptor protein that recruits signalling proteins to Toll-like receptors (TLRs), with the consequent induction of various immune responses. These data suggest that multiple scavenger receptors recognise Ecrg4(71–132) and transduce its signals, together with TLRs, in microglia. Nature Publishing Group UK 2018-03-06 /pmc/articles/PMC5840397/ /pubmed/29511297 http://dx.doi.org/10.1038/s41598-018-22440-4 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Moriguchi, Tetsuo
Takeda, Shuji
Iwashita, Shinzo
Enomoto, Kei
Sawamura, Tatsuya
Koshimizu, Uichi
Kondo, Toru
Ecrg4 peptide is the ligand of multiple scavenger receptors
title Ecrg4 peptide is the ligand of multiple scavenger receptors
title_full Ecrg4 peptide is the ligand of multiple scavenger receptors
title_fullStr Ecrg4 peptide is the ligand of multiple scavenger receptors
title_full_unstemmed Ecrg4 peptide is the ligand of multiple scavenger receptors
title_short Ecrg4 peptide is the ligand of multiple scavenger receptors
title_sort ecrg4 peptide is the ligand of multiple scavenger receptors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840397/
https://www.ncbi.nlm.nih.gov/pubmed/29511297
http://dx.doi.org/10.1038/s41598-018-22440-4
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