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Identification of TSPAN4 as Novel Histamine H(4) Receptor Interactor
The histamine H(4) receptor (H(4)R) is a G protein-coupled receptor that is predominantly expressed on immune cells and considered to be an important drug target for various inflammatory disorders. Like most GPCRs, the H(4)R activates G proteins and recruits β-arrestins upon phosphorylation by GPCR...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8394291/ https://www.ncbi.nlm.nih.gov/pubmed/34439793 http://dx.doi.org/10.3390/biom11081127 |
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author | Ma, Xiaoyuan Verweij, Eléonore W. E. Siderius, Marco Leurs, Rob Vischer, Henry F. |
author_facet | Ma, Xiaoyuan Verweij, Eléonore W. E. Siderius, Marco Leurs, Rob Vischer, Henry F. |
author_sort | Ma, Xiaoyuan |
collection | PubMed |
description | The histamine H(4) receptor (H(4)R) is a G protein-coupled receptor that is predominantly expressed on immune cells and considered to be an important drug target for various inflammatory disorders. Like most GPCRs, the H(4)R activates G proteins and recruits β-arrestins upon phosphorylation by GPCR kinases to induce cellular signaling in response to agonist stimulation. However, in the last decade, novel GPCR-interacting proteins have been identified that may regulate GPCR functioning. In this study, a split-ubiquitin membrane yeast two-hybrid assay was used to identify H(4)R interactors in a Jurkat T cell line cDNA library. Forty-three novel H(4)R interactors were identified, of which 17 have also been previously observed in MYTH screens to interact with other GPCR subtypes. The interaction of H(4)R with the tetraspanin TSPAN4 was confirmed in transfected cells using bioluminescence resonance energy transfer, bimolecular fluorescence complementation, and co-immunoprecipitation. Histamine stimulation reduced the interaction between H(4)R and TSPAN4, but TSPAN4 did not affect H(4)R-mediated G protein signaling. Nonetheless, the identification of novel GPCR interactors by MYTH is a starting point to further investigate the regulation of GPCR signaling. |
format | Online Article Text |
id | pubmed-8394291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83942912021-08-28 Identification of TSPAN4 as Novel Histamine H(4) Receptor Interactor Ma, Xiaoyuan Verweij, Eléonore W. E. Siderius, Marco Leurs, Rob Vischer, Henry F. Biomolecules Article The histamine H(4) receptor (H(4)R) is a G protein-coupled receptor that is predominantly expressed on immune cells and considered to be an important drug target for various inflammatory disorders. Like most GPCRs, the H(4)R activates G proteins and recruits β-arrestins upon phosphorylation by GPCR kinases to induce cellular signaling in response to agonist stimulation. However, in the last decade, novel GPCR-interacting proteins have been identified that may regulate GPCR functioning. In this study, a split-ubiquitin membrane yeast two-hybrid assay was used to identify H(4)R interactors in a Jurkat T cell line cDNA library. Forty-three novel H(4)R interactors were identified, of which 17 have also been previously observed in MYTH screens to interact with other GPCR subtypes. The interaction of H(4)R with the tetraspanin TSPAN4 was confirmed in transfected cells using bioluminescence resonance energy transfer, bimolecular fluorescence complementation, and co-immunoprecipitation. Histamine stimulation reduced the interaction between H(4)R and TSPAN4, but TSPAN4 did not affect H(4)R-mediated G protein signaling. Nonetheless, the identification of novel GPCR interactors by MYTH is a starting point to further investigate the regulation of GPCR signaling. MDPI 2021-07-30 /pmc/articles/PMC8394291/ /pubmed/34439793 http://dx.doi.org/10.3390/biom11081127 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ma, Xiaoyuan Verweij, Eléonore W. E. Siderius, Marco Leurs, Rob Vischer, Henry F. Identification of TSPAN4 as Novel Histamine H(4) Receptor Interactor |
title | Identification of TSPAN4 as Novel Histamine H(4) Receptor Interactor |
title_full | Identification of TSPAN4 as Novel Histamine H(4) Receptor Interactor |
title_fullStr | Identification of TSPAN4 as Novel Histamine H(4) Receptor Interactor |
title_full_unstemmed | Identification of TSPAN4 as Novel Histamine H(4) Receptor Interactor |
title_short | Identification of TSPAN4 as Novel Histamine H(4) Receptor Interactor |
title_sort | identification of tspan4 as novel histamine h(4) receptor interactor |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8394291/ https://www.ncbi.nlm.nih.gov/pubmed/34439793 http://dx.doi.org/10.3390/biom11081127 |
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