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Live-Cell FRET Imaging Reveals a Role of Extracellular Signal-Regulated Kinase Activity Dynamics in Thymocyte Motility
Extracellular signal-regulated kinase (ERK) plays critical roles in T cell development in the thymus. Nevertheless, the dynamics of ERK activity and the role of ERK in regulating thymocyte motility remain largely unknown due to technical limitations. To visualize ERK activity in thymocytes, we here...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6277225/ https://www.ncbi.nlm.nih.gov/pubmed/30508722 http://dx.doi.org/10.1016/j.isci.2018.11.025 |
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author | Konishi, Yoshinobu Terai, Kenta Furuta, Yasuhide Kiyonari, Hiroshi Abe, Takaya Ueda, Yoshihiro Kinashi, Tatsuo Hamazaki, Yoko Takaori-Kondo, Akifumi Matsuda, Michiyuki |
author_facet | Konishi, Yoshinobu Terai, Kenta Furuta, Yasuhide Kiyonari, Hiroshi Abe, Takaya Ueda, Yoshihiro Kinashi, Tatsuo Hamazaki, Yoko Takaori-Kondo, Akifumi Matsuda, Michiyuki |
author_sort | Konishi, Yoshinobu |
collection | PubMed |
description | Extracellular signal-regulated kinase (ERK) plays critical roles in T cell development in the thymus. Nevertheless, the dynamics of ERK activity and the role of ERK in regulating thymocyte motility remain largely unknown due to technical limitations. To visualize ERK activity in thymocytes, we here developed knockin reporter mice expressing a Förster/fluorescence resonance energy transfer (FRET)-based biosensor for ERK from the ROSA26 locus. Live imaging of thymocytes isolated from the reporter mice revealed that ERK regulates thymocyte motility in a subtype-specific manner. Negative correlation between ERK activity and motility was observed in CD4/CD8 double-positive thymocytes and CD8 single-positive thymocytes, but not in CD4 single-positive thymocytes. Interestingly, however, the temporal deviations of ERK activity from the average correlate with the motility of CD4 single-positive thymocytes. Thus, live-cell FRET imaging will open a window to understanding the dynamic nature and the diverse functions of ERK signaling in T cell biology. |
format | Online Article Text |
id | pubmed-6277225 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-62772252018-12-14 Live-Cell FRET Imaging Reveals a Role of Extracellular Signal-Regulated Kinase Activity Dynamics in Thymocyte Motility Konishi, Yoshinobu Terai, Kenta Furuta, Yasuhide Kiyonari, Hiroshi Abe, Takaya Ueda, Yoshihiro Kinashi, Tatsuo Hamazaki, Yoko Takaori-Kondo, Akifumi Matsuda, Michiyuki iScience Article Extracellular signal-regulated kinase (ERK) plays critical roles in T cell development in the thymus. Nevertheless, the dynamics of ERK activity and the role of ERK in regulating thymocyte motility remain largely unknown due to technical limitations. To visualize ERK activity in thymocytes, we here developed knockin reporter mice expressing a Förster/fluorescence resonance energy transfer (FRET)-based biosensor for ERK from the ROSA26 locus. Live imaging of thymocytes isolated from the reporter mice revealed that ERK regulates thymocyte motility in a subtype-specific manner. Negative correlation between ERK activity and motility was observed in CD4/CD8 double-positive thymocytes and CD8 single-positive thymocytes, but not in CD4 single-positive thymocytes. Interestingly, however, the temporal deviations of ERK activity from the average correlate with the motility of CD4 single-positive thymocytes. Thus, live-cell FRET imaging will open a window to understanding the dynamic nature and the diverse functions of ERK signaling in T cell biology. Elsevier 2018-11-20 /pmc/articles/PMC6277225/ /pubmed/30508722 http://dx.doi.org/10.1016/j.isci.2018.11.025 Text en © 2018 The Authors 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 | Article Konishi, Yoshinobu Terai, Kenta Furuta, Yasuhide Kiyonari, Hiroshi Abe, Takaya Ueda, Yoshihiro Kinashi, Tatsuo Hamazaki, Yoko Takaori-Kondo, Akifumi Matsuda, Michiyuki Live-Cell FRET Imaging Reveals a Role of Extracellular Signal-Regulated Kinase Activity Dynamics in Thymocyte Motility |
title | Live-Cell FRET Imaging Reveals a Role of Extracellular Signal-Regulated Kinase Activity Dynamics in Thymocyte Motility |
title_full | Live-Cell FRET Imaging Reveals a Role of Extracellular Signal-Regulated Kinase Activity Dynamics in Thymocyte Motility |
title_fullStr | Live-Cell FRET Imaging Reveals a Role of Extracellular Signal-Regulated Kinase Activity Dynamics in Thymocyte Motility |
title_full_unstemmed | Live-Cell FRET Imaging Reveals a Role of Extracellular Signal-Regulated Kinase Activity Dynamics in Thymocyte Motility |
title_short | Live-Cell FRET Imaging Reveals a Role of Extracellular Signal-Regulated Kinase Activity Dynamics in Thymocyte Motility |
title_sort | live-cell fret imaging reveals a role of extracellular signal-regulated kinase activity dynamics in thymocyte motility |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6277225/ https://www.ncbi.nlm.nih.gov/pubmed/30508722 http://dx.doi.org/10.1016/j.isci.2018.11.025 |
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