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A Cre-dependent reporter mouse for quantitative real-time imaging of Protein Kinase A activity dynamics
Intracellular signaling dynamics play a crucial role in cell function. Protein kinase A (PKA) is a key signaling molecule that has diverse functions, from regulating metabolism and brain activity to guiding development and cancer progression. We previously developed an optical reporter, FLIM-AKAR, t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10635033/ https://www.ncbi.nlm.nih.gov/pubmed/37961214 http://dx.doi.org/10.1101/2023.10.31.565028 |
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author | Tilden, Elizabeth I. Maduskar, Aditi Oldenborg, Anna Sabatini, Bernardo L. Chen, Yao |
author_facet | Tilden, Elizabeth I. Maduskar, Aditi Oldenborg, Anna Sabatini, Bernardo L. Chen, Yao |
author_sort | Tilden, Elizabeth I. |
collection | PubMed |
description | Intracellular signaling dynamics play a crucial role in cell function. Protein kinase A (PKA) is a key signaling molecule that has diverse functions, from regulating metabolism and brain activity to guiding development and cancer progression. We previously developed an optical reporter, FLIM-AKAR, that allows for quantitative imaging of PKA activity via fluorescence lifetime imaging microscopy and photometry. However, using viral infection or electroporation for the delivery of FLIM-AKAR is invasive, cannot easily target sparse or hard-to-transfect/infect cell types, and results in variable expression. Here, we developed a reporter mouse, FL-AK, which expresses FLIM-AKAR in a Cre-dependent manner from the ROSA26 locus. FL-AK provides robust and consistent expression of FLIM-AKAR over time. Functionally, the mouse line reports an increase in PKA activity in response to activation of both G(αs) and G(αq)-coupled receptors in brain slices. In vivo, FL-AK reports PKA phosphorylation in response to neuromodulator receptor activation. Thus, FL-AK provides a quantitative, robust, and flexible method to reveal the dynamics of PKA activity in diverse cell types. |
format | Online Article Text |
id | pubmed-10635033 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-106350332023-11-13 A Cre-dependent reporter mouse for quantitative real-time imaging of Protein Kinase A activity dynamics Tilden, Elizabeth I. Maduskar, Aditi Oldenborg, Anna Sabatini, Bernardo L. Chen, Yao bioRxiv Article Intracellular signaling dynamics play a crucial role in cell function. Protein kinase A (PKA) is a key signaling molecule that has diverse functions, from regulating metabolism and brain activity to guiding development and cancer progression. We previously developed an optical reporter, FLIM-AKAR, that allows for quantitative imaging of PKA activity via fluorescence lifetime imaging microscopy and photometry. However, using viral infection or electroporation for the delivery of FLIM-AKAR is invasive, cannot easily target sparse or hard-to-transfect/infect cell types, and results in variable expression. Here, we developed a reporter mouse, FL-AK, which expresses FLIM-AKAR in a Cre-dependent manner from the ROSA26 locus. FL-AK provides robust and consistent expression of FLIM-AKAR over time. Functionally, the mouse line reports an increase in PKA activity in response to activation of both G(αs) and G(αq)-coupled receptors in brain slices. In vivo, FL-AK reports PKA phosphorylation in response to neuromodulator receptor activation. Thus, FL-AK provides a quantitative, robust, and flexible method to reveal the dynamics of PKA activity in diverse cell types. Cold Spring Harbor Laboratory 2023-11-02 /pmc/articles/PMC10635033/ /pubmed/37961214 http://dx.doi.org/10.1101/2023.10.31.565028 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Tilden, Elizabeth I. Maduskar, Aditi Oldenborg, Anna Sabatini, Bernardo L. Chen, Yao A Cre-dependent reporter mouse for quantitative real-time imaging of Protein Kinase A activity dynamics |
title | A Cre-dependent reporter mouse for quantitative real-time imaging of Protein Kinase A activity dynamics |
title_full | A Cre-dependent reporter mouse for quantitative real-time imaging of Protein Kinase A activity dynamics |
title_fullStr | A Cre-dependent reporter mouse for quantitative real-time imaging of Protein Kinase A activity dynamics |
title_full_unstemmed | A Cre-dependent reporter mouse for quantitative real-time imaging of Protein Kinase A activity dynamics |
title_short | A Cre-dependent reporter mouse for quantitative real-time imaging of Protein Kinase A activity dynamics |
title_sort | cre-dependent reporter mouse for quantitative real-time imaging of protein kinase a activity dynamics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10635033/ https://www.ncbi.nlm.nih.gov/pubmed/37961214 http://dx.doi.org/10.1101/2023.10.31.565028 |
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