The Lifeact-EGFP mouse is a translationally controlled fluorescent reporter of T cell activation
It has become increasingly evident that T cell functions are subject to translational control in addition to transcriptional regulation. Live imaging of CD8+ T cells isolated from the Lifeact-EGFP mouse reveals that they exhibit a gain in fluorescence intensity following engagement of cognate tumour...
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Veröffentlicht in: | Journal of cell science 2020-01 |
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creator | Galeano Niño, Jorge Luis Tay, Szun S Tearle, Jacqueline L E Xie, Jianling Govendir, Matt A Kempe, Daryan Mazalo, Jessica Drew, Alexander P Colakoglu, Feyza Kummerfeld, Sarah K Proud, Christopher G Biro, Maté |
description | It has become increasingly evident that T cell functions are subject to translational control in addition to transcriptional regulation. Live imaging of CD8+ T cells isolated from the Lifeact-EGFP mouse reveals that they exhibit a gain in fluorescence intensity following engagement of cognate tumour target cells. The GFP signal increase is governed by Erk-dependent distal TCR signalling and its magnitude correlates with IFN-γ and TNF-α production, hallmarks of T cell activation. Enhanced fluorescence is due to increased translation of Lifeact-EGFP protein, without an associated increase in messenger RNA. Activation-induced gains in fluorescence are also observed in naïve and CD4+ T cells from the Lifeact-EGFP reporter, and are readily detected by both flow cytometry and live cell microscopy. This unique, translationally controlled reporter of effector T cell activation simultaneously enables tracking of cell morphology, F-actin dynamics and activation state in individual migrating T cells. It is a valuable addition to the limited number of reporters of T cell dynamics and activation, and opens the door to studies of translational activity and heterogeneities in functional T cell responses in situ. |
doi_str_mv | 10.1242/jcs.238014 |
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Live imaging of CD8+ T cells isolated from the Lifeact-EGFP mouse reveals that they exhibit a gain in fluorescence intensity following engagement of cognate tumour target cells. The GFP signal increase is governed by Erk-dependent distal TCR signalling and its magnitude correlates with IFN-γ and TNF-α production, hallmarks of T cell activation. Enhanced fluorescence is due to increased translation of Lifeact-EGFP protein, without an associated increase in messenger RNA. Activation-induced gains in fluorescence are also observed in naïve and CD4+ T cells from the Lifeact-EGFP reporter, and are readily detected by both flow cytometry and live cell microscopy. This unique, translationally controlled reporter of effector T cell activation simultaneously enables tracking of cell morphology, F-actin dynamics and activation state in individual migrating T cells. 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Live imaging of CD8+ T cells isolated from the Lifeact-EGFP mouse reveals that they exhibit a gain in fluorescence intensity following engagement of cognate tumour target cells. The GFP signal increase is governed by Erk-dependent distal TCR signalling and its magnitude correlates with IFN-γ and TNF-α production, hallmarks of T cell activation. Enhanced fluorescence is due to increased translation of Lifeact-EGFP protein, without an associated increase in messenger RNA. Activation-induced gains in fluorescence are also observed in naïve and CD4+ T cells from the Lifeact-EGFP reporter, and are readily detected by both flow cytometry and live cell microscopy. This unique, translationally controlled reporter of effector T cell activation simultaneously enables tracking of cell morphology, F-actin dynamics and activation state in individual migrating T cells. 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source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection; Company of Biologists |
title | The Lifeact-EGFP mouse is a translationally controlled fluorescent reporter of T cell activation |
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