Cargando…

Genetically encoded tools for in vivo G‐protein‐coupled receptor agonist detection at cellular resolution

G‐protein‐coupled receptors (GPCRs) are the most abundant receptor type in the human body and are responsible for regulating many physiological processes, such as sensation, cognition, muscle contraction and metabolism. Further, GPCRs are widely expressed in the brain where their agonists make up a...

Descripción completa

Detalles Bibliográficos
Autores principales: Kroning, Kayla E., Wang, Wenjing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9708909/
https://www.ncbi.nlm.nih.gov/pubmed/36446954
http://dx.doi.org/10.1002/ctm2.1124
_version_ 1784841044941078528
author Kroning, Kayla E.
Wang, Wenjing
author_facet Kroning, Kayla E.
Wang, Wenjing
author_sort Kroning, Kayla E.
collection PubMed
description G‐protein‐coupled receptors (GPCRs) are the most abundant receptor type in the human body and are responsible for regulating many physiological processes, such as sensation, cognition, muscle contraction and metabolism. Further, GPCRs are widely expressed in the brain where their agonists make up a large number of neurotransmitters and neuromodulators. Due to the importance of GPCRs in human physiology, genetically encoded sensors have been engineered to detect GPCR agonists at cellular resolution in vivo. These sensors can be placed into two main categories: those that offer real‐time information on the signalling dynamics of GPCR agonists and those that integrate the GPCR agonist signal into a permanent, quantifiable mark that can be used to detect GPCR agonist localisation in a large brain area. In this review, we discuss the various designs of real‐time and integration sensors, their advantages and limitations, and some in vivo applications. We also discuss the potential of using real‐time and integrator sensors together to identify neuronal circuits affected by endogenous GPCR agonists and perform detailed characterisations of the spatiotemporal dynamics of GPCR agonist release in those circuits. By using these sensors together, the overall knowledge of GPCR‐mediated signalling can be expanded.
format Online
Article
Text
id pubmed-9708909
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-97089092022-12-02 Genetically encoded tools for in vivo G‐protein‐coupled receptor agonist detection at cellular resolution Kroning, Kayla E. Wang, Wenjing Clin Transl Med Reviews G‐protein‐coupled receptors (GPCRs) are the most abundant receptor type in the human body and are responsible for regulating many physiological processes, such as sensation, cognition, muscle contraction and metabolism. Further, GPCRs are widely expressed in the brain where their agonists make up a large number of neurotransmitters and neuromodulators. Due to the importance of GPCRs in human physiology, genetically encoded sensors have been engineered to detect GPCR agonists at cellular resolution in vivo. These sensors can be placed into two main categories: those that offer real‐time information on the signalling dynamics of GPCR agonists and those that integrate the GPCR agonist signal into a permanent, quantifiable mark that can be used to detect GPCR agonist localisation in a large brain area. In this review, we discuss the various designs of real‐time and integration sensors, their advantages and limitations, and some in vivo applications. We also discuss the potential of using real‐time and integrator sensors together to identify neuronal circuits affected by endogenous GPCR agonists and perform detailed characterisations of the spatiotemporal dynamics of GPCR agonist release in those circuits. By using these sensors together, the overall knowledge of GPCR‐mediated signalling can be expanded. John Wiley and Sons Inc. 2022-11-29 /pmc/articles/PMC9708909/ /pubmed/36446954 http://dx.doi.org/10.1002/ctm2.1124 Text en © 2022 The Authors. Clinical and Translational Medicine published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Kroning, Kayla E.
Wang, Wenjing
Genetically encoded tools for in vivo G‐protein‐coupled receptor agonist detection at cellular resolution
title Genetically encoded tools for in vivo G‐protein‐coupled receptor agonist detection at cellular resolution
title_full Genetically encoded tools for in vivo G‐protein‐coupled receptor agonist detection at cellular resolution
title_fullStr Genetically encoded tools for in vivo G‐protein‐coupled receptor agonist detection at cellular resolution
title_full_unstemmed Genetically encoded tools for in vivo G‐protein‐coupled receptor agonist detection at cellular resolution
title_short Genetically encoded tools for in vivo G‐protein‐coupled receptor agonist detection at cellular resolution
title_sort genetically encoded tools for in vivo g‐protein‐coupled receptor agonist detection at cellular resolution
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9708909/
https://www.ncbi.nlm.nih.gov/pubmed/36446954
http://dx.doi.org/10.1002/ctm2.1124
work_keys_str_mv AT kroningkaylae geneticallyencodedtoolsforinvivogproteincoupledreceptoragonistdetectionatcellularresolution
AT wangwenjing geneticallyencodedtoolsforinvivogproteincoupledreceptoragonistdetectionatcellularresolution