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AMPK Amplifies IL2–STAT5 Signaling to Maintain Stability of Regulatory T Cells in Aged Mice

AMP-activated protein kinase (AMPK), an important regulator of the aging process, is expressed in various immune cells. However, its role in regulatory T cell (Treg) stability during aging is poorly understood. Here, we addressed the role of AMPK in Treg function and stability during aging by genera...

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Autores principales: Pokhrel, Ram Hari, Kang, Ben, Timilshina, Maheshwor, Chang, Jae-Hoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604214/
https://www.ncbi.nlm.nih.gov/pubmed/36293240
http://dx.doi.org/10.3390/ijms232012384
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author Pokhrel, Ram Hari
Kang, Ben
Timilshina, Maheshwor
Chang, Jae-Hoon
author_facet Pokhrel, Ram Hari
Kang, Ben
Timilshina, Maheshwor
Chang, Jae-Hoon
author_sort Pokhrel, Ram Hari
collection PubMed
description AMP-activated protein kinase (AMPK), an important regulator of the aging process, is expressed in various immune cells. However, its role in regulatory T cell (Treg) stability during aging is poorly understood. Here, we addressed the role of AMPK in Treg function and stability during aging by generating Treg-specific AMPKα1 knockout mice. In this study, we found that AMPKα1-deficient Tregs failed to control inflammation as effectively as normal Tregs did during aging. AMPK knockout from Tregs reduces STAT5 phosphorylation in response to interleukin (IL)-2 stimulation, thereby destabilizing Tregs by decreasing CD25 expression. Thus, our study addressed the role of AMPK in Tregs in sensing IL-2 signaling to amplify STAT5 phosphorylation, which, in turn, supports Treg stability by maintaining CD25 expression and controlling inflamm-aging.
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spelling pubmed-96042142022-10-27 AMPK Amplifies IL2–STAT5 Signaling to Maintain Stability of Regulatory T Cells in Aged Mice Pokhrel, Ram Hari Kang, Ben Timilshina, Maheshwor Chang, Jae-Hoon Int J Mol Sci Article AMP-activated protein kinase (AMPK), an important regulator of the aging process, is expressed in various immune cells. However, its role in regulatory T cell (Treg) stability during aging is poorly understood. Here, we addressed the role of AMPK in Treg function and stability during aging by generating Treg-specific AMPKα1 knockout mice. In this study, we found that AMPKα1-deficient Tregs failed to control inflammation as effectively as normal Tregs did during aging. AMPK knockout from Tregs reduces STAT5 phosphorylation in response to interleukin (IL)-2 stimulation, thereby destabilizing Tregs by decreasing CD25 expression. Thus, our study addressed the role of AMPK in Tregs in sensing IL-2 signaling to amplify STAT5 phosphorylation, which, in turn, supports Treg stability by maintaining CD25 expression and controlling inflamm-aging. MDPI 2022-10-16 /pmc/articles/PMC9604214/ /pubmed/36293240 http://dx.doi.org/10.3390/ijms232012384 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pokhrel, Ram Hari
Kang, Ben
Timilshina, Maheshwor
Chang, Jae-Hoon
AMPK Amplifies IL2–STAT5 Signaling to Maintain Stability of Regulatory T Cells in Aged Mice
title AMPK Amplifies IL2–STAT5 Signaling to Maintain Stability of Regulatory T Cells in Aged Mice
title_full AMPK Amplifies IL2–STAT5 Signaling to Maintain Stability of Regulatory T Cells in Aged Mice
title_fullStr AMPK Amplifies IL2–STAT5 Signaling to Maintain Stability of Regulatory T Cells in Aged Mice
title_full_unstemmed AMPK Amplifies IL2–STAT5 Signaling to Maintain Stability of Regulatory T Cells in Aged Mice
title_short AMPK Amplifies IL2–STAT5 Signaling to Maintain Stability of Regulatory T Cells in Aged Mice
title_sort ampk amplifies il2–stat5 signaling to maintain stability of regulatory t cells in aged mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604214/
https://www.ncbi.nlm.nih.gov/pubmed/36293240
http://dx.doi.org/10.3390/ijms232012384
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