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A Protocol for FRET-Based Live-Cell Imaging in Microglia

This protocol highlights the use of FRET-based biosensors to investigate signaling events during microglia activation in real time. Understanding microglia activation has gained momentum as it can help decipher signaling mechanisms underlying the neurodegenerative process occurring in neurological d...

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Detalles Bibliográficos
Autores principales: Socodato, Renato, Melo, Pedro, Ferraz-Nogueira, José P., Portugal, Camila C., Relvas, João B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757332/
https://www.ncbi.nlm.nih.gov/pubmed/33377041
http://dx.doi.org/10.1016/j.xpro.2020.100147
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author Socodato, Renato
Melo, Pedro
Ferraz-Nogueira, José P.
Portugal, Camila C.
Relvas, João B.
author_facet Socodato, Renato
Melo, Pedro
Ferraz-Nogueira, José P.
Portugal, Camila C.
Relvas, João B.
author_sort Socodato, Renato
collection PubMed
description This protocol highlights the use of FRET-based biosensors to investigate signaling events during microglia activation in real time. Understanding microglia activation has gained momentum as it can help decipher signaling mechanisms underlying the neurodegenerative process occurring in neurological disorders. Unlike more traditional methods widely employed in the microglia field, FRET allows microglia signaling events to be studied in real time with exquisite subcellular resolution. However, FRET-based live-cell imaging requires application-specific biosensors and specialized imaging systems, limiting its use in in vivo studies. For complete details on the use and execution of this protocol, please refer to Socodato et al. (2020), Portugal et al. (2017), and Socodato et al. (2018).
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spelling pubmed-77573322020-12-28 A Protocol for FRET-Based Live-Cell Imaging in Microglia Socodato, Renato Melo, Pedro Ferraz-Nogueira, José P. Portugal, Camila C. Relvas, João B. STAR Protoc Protocol This protocol highlights the use of FRET-based biosensors to investigate signaling events during microglia activation in real time. Understanding microglia activation has gained momentum as it can help decipher signaling mechanisms underlying the neurodegenerative process occurring in neurological disorders. Unlike more traditional methods widely employed in the microglia field, FRET allows microglia signaling events to be studied in real time with exquisite subcellular resolution. However, FRET-based live-cell imaging requires application-specific biosensors and specialized imaging systems, limiting its use in in vivo studies. For complete details on the use and execution of this protocol, please refer to Socodato et al. (2020), Portugal et al. (2017), and Socodato et al. (2018). Elsevier 2020-10-23 /pmc/articles/PMC7757332/ /pubmed/33377041 http://dx.doi.org/10.1016/j.xpro.2020.100147 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Socodato, Renato
Melo, Pedro
Ferraz-Nogueira, José P.
Portugal, Camila C.
Relvas, João B.
A Protocol for FRET-Based Live-Cell Imaging in Microglia
title A Protocol for FRET-Based Live-Cell Imaging in Microglia
title_full A Protocol for FRET-Based Live-Cell Imaging in Microglia
title_fullStr A Protocol for FRET-Based Live-Cell Imaging in Microglia
title_full_unstemmed A Protocol for FRET-Based Live-Cell Imaging in Microglia
title_short A Protocol for FRET-Based Live-Cell Imaging in Microglia
title_sort protocol for fret-based live-cell imaging in microglia
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757332/
https://www.ncbi.nlm.nih.gov/pubmed/33377041
http://dx.doi.org/10.1016/j.xpro.2020.100147
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