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Agonist-Directed Desensitization of the β(2)-Adrenergic Receptor

The β(2)-adrenergic receptor (β(2)AR) agonists with reduced tachyphylaxis may offer new therapeutic agents with improved tolerance profile. However, receptor desensitization assays are often inferred at the single signaling molecule level, thus ligand-directed desensitization is poorly understood. H...

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Detalles Bibliográficos
Autores principales: Goral, Vasiliy, Jin, Yan, Sun, Haiyan, Ferrie, Ann M., Wu, Qi, Fang, Ye
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3082563/
https://www.ncbi.nlm.nih.gov/pubmed/21541288
http://dx.doi.org/10.1371/journal.pone.0019282
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author Goral, Vasiliy
Jin, Yan
Sun, Haiyan
Ferrie, Ann M.
Wu, Qi
Fang, Ye
author_facet Goral, Vasiliy
Jin, Yan
Sun, Haiyan
Ferrie, Ann M.
Wu, Qi
Fang, Ye
author_sort Goral, Vasiliy
collection PubMed
description The β(2)-adrenergic receptor (β(2)AR) agonists with reduced tachyphylaxis may offer new therapeutic agents with improved tolerance profile. However, receptor desensitization assays are often inferred at the single signaling molecule level, thus ligand-directed desensitization is poorly understood. Here we report a label-free biosensor whole cell assay with microfluidics to determine ligand-directed desensitization of the β(2)AR. Together with mechanistic deconvolution using small molecule inhibitors, the receptor desensitization and resensitization patterns under the short-term agonist exposure manifested the long-acting agonism of salmeterol, and differentiated the mechanisms of agonist-directed desensitization between a full agonist epinephrine and a partial agonist pindolol. This study reveals the cellular mechanisms of agonist-selective β(2)AR desensitization at the whole cell level.
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spelling pubmed-30825632011-05-03 Agonist-Directed Desensitization of the β(2)-Adrenergic Receptor Goral, Vasiliy Jin, Yan Sun, Haiyan Ferrie, Ann M. Wu, Qi Fang, Ye PLoS One Research Article The β(2)-adrenergic receptor (β(2)AR) agonists with reduced tachyphylaxis may offer new therapeutic agents with improved tolerance profile. However, receptor desensitization assays are often inferred at the single signaling molecule level, thus ligand-directed desensitization is poorly understood. Here we report a label-free biosensor whole cell assay with microfluidics to determine ligand-directed desensitization of the β(2)AR. Together with mechanistic deconvolution using small molecule inhibitors, the receptor desensitization and resensitization patterns under the short-term agonist exposure manifested the long-acting agonism of salmeterol, and differentiated the mechanisms of agonist-directed desensitization between a full agonist epinephrine and a partial agonist pindolol. This study reveals the cellular mechanisms of agonist-selective β(2)AR desensitization at the whole cell level. Public Library of Science 2011-04-26 /pmc/articles/PMC3082563/ /pubmed/21541288 http://dx.doi.org/10.1371/journal.pone.0019282 Text en Goral et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Goral, Vasiliy
Jin, Yan
Sun, Haiyan
Ferrie, Ann M.
Wu, Qi
Fang, Ye
Agonist-Directed Desensitization of the β(2)-Adrenergic Receptor
title Agonist-Directed Desensitization of the β(2)-Adrenergic Receptor
title_full Agonist-Directed Desensitization of the β(2)-Adrenergic Receptor
title_fullStr Agonist-Directed Desensitization of the β(2)-Adrenergic Receptor
title_full_unstemmed Agonist-Directed Desensitization of the β(2)-Adrenergic Receptor
title_short Agonist-Directed Desensitization of the β(2)-Adrenergic Receptor
title_sort agonist-directed desensitization of the β(2)-adrenergic receptor
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3082563/
https://www.ncbi.nlm.nih.gov/pubmed/21541288
http://dx.doi.org/10.1371/journal.pone.0019282
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