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Unspecific CTL Killing Is Enhanced by High Glucose via TNF-Related Apoptosis-Inducing Ligand

TNF-related apoptosis inducing ligand (TRAIL) is expressed on cytotoxic T lymphocytes (CTLs) and TRAIL is linked to progression of diabetes. However, the impact of high glucose on TRAIL expression and its related killing function in CTLs still remains largely elusive. Here, we report that TRAIL is s...

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Autores principales: Yang, Wenjuan, Denger, Andreas, Diener, Caroline, Küppers, Frederic, Soriano-Baguet, Leticia, Schäfer, Gertrud, Yanamandra, Archana K., Zhao, Renping, Knörck, Arne, Schwarz, Eva C., Hart, Martin, Lammert, Frank, Roma, Leticia Prates, Brenner, Dirk, Christidis, Grigorios, Helms, Volkhard, Meese, Eckart, Hoth, Markus, Qu, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8899024/
https://www.ncbi.nlm.nih.gov/pubmed/35265081
http://dx.doi.org/10.3389/fimmu.2022.831680
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author Yang, Wenjuan
Denger, Andreas
Diener, Caroline
Küppers, Frederic
Soriano-Baguet, Leticia
Schäfer, Gertrud
Yanamandra, Archana K.
Zhao, Renping
Knörck, Arne
Schwarz, Eva C.
Hart, Martin
Lammert, Frank
Roma, Leticia Prates
Brenner, Dirk
Christidis, Grigorios
Helms, Volkhard
Meese, Eckart
Hoth, Markus
Qu, Bin
author_facet Yang, Wenjuan
Denger, Andreas
Diener, Caroline
Küppers, Frederic
Soriano-Baguet, Leticia
Schäfer, Gertrud
Yanamandra, Archana K.
Zhao, Renping
Knörck, Arne
Schwarz, Eva C.
Hart, Martin
Lammert, Frank
Roma, Leticia Prates
Brenner, Dirk
Christidis, Grigorios
Helms, Volkhard
Meese, Eckart
Hoth, Markus
Qu, Bin
author_sort Yang, Wenjuan
collection PubMed
description TNF-related apoptosis inducing ligand (TRAIL) is expressed on cytotoxic T lymphocytes (CTLs) and TRAIL is linked to progression of diabetes. However, the impact of high glucose on TRAIL expression and its related killing function in CTLs still remains largely elusive. Here, we report that TRAIL is substantially up-regulated in CTLs in environments with high glucose (HG) both in vitro and in vivo. Non-mitochondrial reactive oxygen species, NFκB and PI3K/Akt are essential in HG-induced TRAIL upregulation in CTLs. TRAIL(high) CTLs induce apoptosis of pancreatic beta cell line 1.4E7. Treatment with metformin and vitamin D reduces HG-enhanced expression of TRAIL in CTLs and coherently protects 1.4E7 cells from TRAIL-mediated apoptosis. Our work suggests that HG-induced TRAIL(high) CTLs might contribute to the destruction of pancreatic beta cells in a hyperglycemia condition.
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spelling pubmed-88990242022-03-08 Unspecific CTL Killing Is Enhanced by High Glucose via TNF-Related Apoptosis-Inducing Ligand Yang, Wenjuan Denger, Andreas Diener, Caroline Küppers, Frederic Soriano-Baguet, Leticia Schäfer, Gertrud Yanamandra, Archana K. Zhao, Renping Knörck, Arne Schwarz, Eva C. Hart, Martin Lammert, Frank Roma, Leticia Prates Brenner, Dirk Christidis, Grigorios Helms, Volkhard Meese, Eckart Hoth, Markus Qu, Bin Front Immunol Immunology TNF-related apoptosis inducing ligand (TRAIL) is expressed on cytotoxic T lymphocytes (CTLs) and TRAIL is linked to progression of diabetes. However, the impact of high glucose on TRAIL expression and its related killing function in CTLs still remains largely elusive. Here, we report that TRAIL is substantially up-regulated in CTLs in environments with high glucose (HG) both in vitro and in vivo. Non-mitochondrial reactive oxygen species, NFκB and PI3K/Akt are essential in HG-induced TRAIL upregulation in CTLs. TRAIL(high) CTLs induce apoptosis of pancreatic beta cell line 1.4E7. Treatment with metformin and vitamin D reduces HG-enhanced expression of TRAIL in CTLs and coherently protects 1.4E7 cells from TRAIL-mediated apoptosis. Our work suggests that HG-induced TRAIL(high) CTLs might contribute to the destruction of pancreatic beta cells in a hyperglycemia condition. Frontiers Media S.A. 2022-02-21 /pmc/articles/PMC8899024/ /pubmed/35265081 http://dx.doi.org/10.3389/fimmu.2022.831680 Text en Copyright © 2022 Yang, Denger, Diener, Küppers, Soriano-Baguet, Schäfer, Yanamandra, Zhao, Knörck, Schwarz, Hart, Lammert, Roma, Brenner, Christidis, Helms, Meese, Hoth and Qu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Yang, Wenjuan
Denger, Andreas
Diener, Caroline
Küppers, Frederic
Soriano-Baguet, Leticia
Schäfer, Gertrud
Yanamandra, Archana K.
Zhao, Renping
Knörck, Arne
Schwarz, Eva C.
Hart, Martin
Lammert, Frank
Roma, Leticia Prates
Brenner, Dirk
Christidis, Grigorios
Helms, Volkhard
Meese, Eckart
Hoth, Markus
Qu, Bin
Unspecific CTL Killing Is Enhanced by High Glucose via TNF-Related Apoptosis-Inducing Ligand
title Unspecific CTL Killing Is Enhanced by High Glucose via TNF-Related Apoptosis-Inducing Ligand
title_full Unspecific CTL Killing Is Enhanced by High Glucose via TNF-Related Apoptosis-Inducing Ligand
title_fullStr Unspecific CTL Killing Is Enhanced by High Glucose via TNF-Related Apoptosis-Inducing Ligand
title_full_unstemmed Unspecific CTL Killing Is Enhanced by High Glucose via TNF-Related Apoptosis-Inducing Ligand
title_short Unspecific CTL Killing Is Enhanced by High Glucose via TNF-Related Apoptosis-Inducing Ligand
title_sort unspecific ctl killing is enhanced by high glucose via tnf-related apoptosis-inducing ligand
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8899024/
https://www.ncbi.nlm.nih.gov/pubmed/35265081
http://dx.doi.org/10.3389/fimmu.2022.831680
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