Super-resolution microscopy compatible fluorescent probes reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics

Glucagon-like peptide-1 receptor is an important regulator of appetite and glucose homeostasis. Here the authors describe super-resolution microscopy and in vivo imaging compatible fluorescent probes, which reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics in islets and br...

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Main Authors: Julia Ast, Anastasia Arvaniti, Nicholas H. F. Fine, Daniela Nasteska, Fiona B. Ashford, Zania Stamataki, Zsombor Koszegi, Andrea Bacon, Ben J. Jones, Maria A. Lucey, Shugo Sasaki, Daniel I. Brierley, Benoit Hastoy, Alejandra Tomas, Giuseppe D’Agostino, Frank Reimann, Francis C. Lynn, Christopher A. Reissaus, Amelia K. Linnemann, Elisa D’Este, Davide Calebiro, Stefan Trapp, Kai Johnsson, Tom Podewin, Johannes Broichhagen, David J. Hodson
Format: Article
Language:English
Published: Nature Publishing Group 2020-01-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-020-14309-w
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spelling doaj-1bec881e08194ff3b4ad84658e0675292021-05-11T08:04:31ZengNature Publishing GroupNature Communications2041-17232020-01-0111111810.1038/s41467-020-14309-wSuper-resolution microscopy compatible fluorescent probes reveal endogenous glucagon-like peptide-1 receptor distribution and dynamicsJulia Ast0Anastasia Arvaniti1Nicholas H. F. Fine2Daniela Nasteska3Fiona B. Ashford4Zania Stamataki5Zsombor Koszegi6Andrea Bacon7Ben J. Jones8Maria A. Lucey9Shugo Sasaki10Daniel I. Brierley11Benoit Hastoy12Alejandra Tomas13Giuseppe D’Agostino14Frank Reimann15Francis C. Lynn16Christopher A. Reissaus17Amelia K. Linnemann18Elisa D’Este19Davide Calebiro20Stefan Trapp21Kai Johnsson22Tom Podewin23Johannes Broichhagen24David J. Hodson25Institute of Metabolism and Systems Research (IMSR), and Centre of Membrane Proteins and Receptors (COMPARE), University of BirminghamInstitute of Metabolism and Systems Research (IMSR), and Centre of Membrane Proteins and Receptors (COMPARE), University of BirminghamInstitute of Metabolism and Systems Research (IMSR), and Centre of Membrane Proteins and Receptors (COMPARE), University of BirminghamInstitute of Metabolism and Systems Research (IMSR), and Centre of Membrane Proteins and Receptors (COMPARE), University of BirminghamInstitute of Metabolism and Systems Research (IMSR), and Centre of Membrane Proteins and Receptors (COMPARE), University of BirminghamCentre for Liver Research, College of Medical and Dental Sciences, Institute for Immunology and Immunotherapy, University of BirminghamInstitute of Metabolism and Systems Research (IMSR), and Centre of Membrane Proteins and Receptors (COMPARE), University of BirminghamGenome Editing Facility, Technology Hub, University of BirminghamDivision of Diabetes, Endocrinology and Metabolism, Section of Investigative Medicine, Imperial College LondonDivision of Diabetes, Endocrinology and Metabolism, Section of Investigative Medicine, Imperial College LondonDiabetes Research Group, BC Children’s Hospital Research Institute, Vancouver, BC, Canada; Department of Surgery, University of British ColumbiaCentre for Cardiovascular and Metabolic Neuroscience, Department of Neuroscience, Physiology & Pharmacology, University College LondonOxford Centre for Diabetes, Endocrinology & Metabolism, University of OxfordDivision of Diabetes, Endocrinology and Metabolism, Section of Cell Biology and Functional Genomics, Imperial College LondonFaculty of Biology, Medicine and Health, University of ManchesterWellcome Trust-MRC Institute of Metabolic Science, University of CambridgeDiabetes Research Group, BC Children’s Hospital Research Institute, Vancouver, BC, Canada; Department of Surgery, University of British ColumbiaDepartment of Pediatrics, Indiana University School of MedicineDepartment of Pediatrics, Indiana University School of MedicineOptical Microscopy Facility, Max Planck Institute for Medical ResearchInstitute of Metabolism and Systems Research (IMSR), and Centre of Membrane Proteins and Receptors (COMPARE), University of BirminghamCentre for Cardiovascular and Metabolic Neuroscience, Department of Neuroscience, Physiology & Pharmacology, University College LondonDepartment of Chemical Biology, Max Planck Institute for Medical ResearchDepartment of Chemical Biology, Max Planck Institute for Medical ResearchDepartment of Chemical Biology, Max Planck Institute for Medical ResearchInstitute of Metabolism and Systems Research (IMSR), and Centre of Membrane Proteins and Receptors (COMPARE), University of BirminghamGlucagon-like peptide-1 receptor is an important regulator of appetite and glucose homeostasis. Here the authors describe super-resolution microscopy and in vivo imaging compatible fluorescent probes, which reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics in islets and brain.https://doi.org/10.1038/s41467-020-14309-w
collection DOAJ
language English
format Article
sources DOAJ
author Julia Ast
Anastasia Arvaniti
Nicholas H. F. Fine
Daniela Nasteska
Fiona B. Ashford
Zania Stamataki
Zsombor Koszegi
Andrea Bacon
Ben J. Jones
Maria A. Lucey
Shugo Sasaki
Daniel I. Brierley
Benoit Hastoy
Alejandra Tomas
Giuseppe D’Agostino
Frank Reimann
Francis C. Lynn
Christopher A. Reissaus
Amelia K. Linnemann
Elisa D’Este
Davide Calebiro
Stefan Trapp
Kai Johnsson
Tom Podewin
Johannes Broichhagen
David J. Hodson
spellingShingle Julia Ast
Anastasia Arvaniti
Nicholas H. F. Fine
Daniela Nasteska
Fiona B. Ashford
Zania Stamataki
Zsombor Koszegi
Andrea Bacon
Ben J. Jones
Maria A. Lucey
Shugo Sasaki
Daniel I. Brierley
Benoit Hastoy
Alejandra Tomas
Giuseppe D’Agostino
Frank Reimann
Francis C. Lynn
Christopher A. Reissaus
Amelia K. Linnemann
Elisa D’Este
Davide Calebiro
Stefan Trapp
Kai Johnsson
Tom Podewin
Johannes Broichhagen
David J. Hodson
Super-resolution microscopy compatible fluorescent probes reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics
Nature Communications
author_facet Julia Ast
Anastasia Arvaniti
Nicholas H. F. Fine
Daniela Nasteska
Fiona B. Ashford
Zania Stamataki
Zsombor Koszegi
Andrea Bacon
Ben J. Jones
Maria A. Lucey
Shugo Sasaki
Daniel I. Brierley
Benoit Hastoy
Alejandra Tomas
Giuseppe D’Agostino
Frank Reimann
Francis C. Lynn
Christopher A. Reissaus
Amelia K. Linnemann
Elisa D’Este
Davide Calebiro
Stefan Trapp
Kai Johnsson
Tom Podewin
Johannes Broichhagen
David J. Hodson
author_sort Julia Ast
title Super-resolution microscopy compatible fluorescent probes reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics
title_short Super-resolution microscopy compatible fluorescent probes reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics
title_full Super-resolution microscopy compatible fluorescent probes reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics
title_fullStr Super-resolution microscopy compatible fluorescent probes reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics
title_full_unstemmed Super-resolution microscopy compatible fluorescent probes reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics
title_sort super-resolution microscopy compatible fluorescent probes reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics
publisher Nature Publishing Group
series Nature Communications
issn 2041-1723
publishDate 2020-01-01
description Glucagon-like peptide-1 receptor is an important regulator of appetite and glucose homeostasis. Here the authors describe super-resolution microscopy and in vivo imaging compatible fluorescent probes, which reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics in islets and brain.
url https://doi.org/10.1038/s41467-020-14309-w
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