Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Ma, Xiaoyuan, Verweij, Eléonore W. E., Siderius, Marco, Leurs, Rob, Vischer, Henry F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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
_version_ 1783743913749643264
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
work_keys_str_mv AT maxiaoyuan identificationoftspan4asnovelhistamineh4receptorinteractor
AT verweijeleonorewe identificationoftspan4asnovelhistamineh4receptorinteractor
AT sideriusmarco identificationoftspan4asnovelhistamineh4receptorinteractor
AT leursrob identificationoftspan4asnovelhistamineh4receptorinteractor
AT vischerhenryf identificationoftspan4asnovelhistamineh4receptorinteractor