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Role of Caspase-10-P13tBID axis in erythropoiesis regulation

Red blood cell production is negatively controlled by the rate of apoptosis at the stage of CFU-E/pro-erythroblast differentiation, depending on the balance between erythropoietin (EPO) levels and activation of the Fas/FasL pathway. At this stage, activation of transient caspases through depolarizat...

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Autores principales: Lamarque, Mathilde, Gautier, Emilie-Fleur, Rodrigues, François, Guillem, Flavia, Bayard, Elisa, Broussard, Cédric, Maciel Trovati, Thiago, Arlet, Jean-Benoît, Mayeux, Patrick, Hermine, Olivier, Courtois, Geneviève
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9883265/
https://www.ncbi.nlm.nih.gov/pubmed/36202990
http://dx.doi.org/10.1038/s41418-022-01066-0
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author Lamarque, Mathilde
Gautier, Emilie-Fleur
Rodrigues, François
Guillem, Flavia
Bayard, Elisa
Broussard, Cédric
Maciel Trovati, Thiago
Arlet, Jean-Benoît
Mayeux, Patrick
Hermine, Olivier
Courtois, Geneviève
author_facet Lamarque, Mathilde
Gautier, Emilie-Fleur
Rodrigues, François
Guillem, Flavia
Bayard, Elisa
Broussard, Cédric
Maciel Trovati, Thiago
Arlet, Jean-Benoît
Mayeux, Patrick
Hermine, Olivier
Courtois, Geneviève
author_sort Lamarque, Mathilde
collection PubMed
description Red blood cell production is negatively controlled by the rate of apoptosis at the stage of CFU-E/pro-erythroblast differentiation, depending on the balance between erythropoietin (EPO) levels and activation of the Fas/FasL pathway. At this stage, activation of transient caspases through depolarization via mitochondrial outer membrane permeabilization (MOMP) is also required for terminal erythroid differentiation. Molecular mechanisms regulating the differential levels of MOMP during differentiation and apoptosis, however, remain poorly understood. Here we show a novel and essential role for the caspase-10-P13-tBID axis in erythroid terminal differentiation. Caspase-10 (but not caspase-8, which is activated during apoptosis) is activated at the early stages of erythroid terminal differentiation leading to the cleavage of P22-BID into P18-tBID, and later into P13-tBID. Erythropoietin (EPO) by inducing casein kinase I alpha (CKIα) expression, which in turn phosphorylates P18-tBID, prevents the generation of MYR-P15-tBID (leading to apoptosis) and allows the generation of P13-tBID by caspase-10. Unlike P15-tBID, P13-tBID is not myristoylated and as such, does not irreversibly anchor the mitochondrial membrane resulting in a transient MOMP. Likewise, transduction of a P13-tBID fragment induces rapid and strong erythroid terminal differentiation. Thus, EPO modulates the pattern of BID cleavage to control the level of MOMP and determines the fate of erythroblasts between apoptosis and differentiation. This pathway is impaired in 5q- myelodysplastic syndromes because of CK1α haplo-insufficiency and may contribute to erythroid differentiation arrest and high sensitivity of this disease to lenalidomide (LEN).
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spelling pubmed-98832652023-01-29 Role of Caspase-10-P13tBID axis in erythropoiesis regulation Lamarque, Mathilde Gautier, Emilie-Fleur Rodrigues, François Guillem, Flavia Bayard, Elisa Broussard, Cédric Maciel Trovati, Thiago Arlet, Jean-Benoît Mayeux, Patrick Hermine, Olivier Courtois, Geneviève Cell Death Differ Article Red blood cell production is negatively controlled by the rate of apoptosis at the stage of CFU-E/pro-erythroblast differentiation, depending on the balance between erythropoietin (EPO) levels and activation of the Fas/FasL pathway. At this stage, activation of transient caspases through depolarization via mitochondrial outer membrane permeabilization (MOMP) is also required for terminal erythroid differentiation. Molecular mechanisms regulating the differential levels of MOMP during differentiation and apoptosis, however, remain poorly understood. Here we show a novel and essential role for the caspase-10-P13-tBID axis in erythroid terminal differentiation. Caspase-10 (but not caspase-8, which is activated during apoptosis) is activated at the early stages of erythroid terminal differentiation leading to the cleavage of P22-BID into P18-tBID, and later into P13-tBID. Erythropoietin (EPO) by inducing casein kinase I alpha (CKIα) expression, which in turn phosphorylates P18-tBID, prevents the generation of MYR-P15-tBID (leading to apoptosis) and allows the generation of P13-tBID by caspase-10. Unlike P15-tBID, P13-tBID is not myristoylated and as such, does not irreversibly anchor the mitochondrial membrane resulting in a transient MOMP. Likewise, transduction of a P13-tBID fragment induces rapid and strong erythroid terminal differentiation. Thus, EPO modulates the pattern of BID cleavage to control the level of MOMP and determines the fate of erythroblasts between apoptosis and differentiation. This pathway is impaired in 5q- myelodysplastic syndromes because of CK1α haplo-insufficiency and may contribute to erythroid differentiation arrest and high sensitivity of this disease to lenalidomide (LEN). Nature Publishing Group UK 2022-10-06 2023-01 /pmc/articles/PMC9883265/ /pubmed/36202990 http://dx.doi.org/10.1038/s41418-022-01066-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lamarque, Mathilde
Gautier, Emilie-Fleur
Rodrigues, François
Guillem, Flavia
Bayard, Elisa
Broussard, Cédric
Maciel Trovati, Thiago
Arlet, Jean-Benoît
Mayeux, Patrick
Hermine, Olivier
Courtois, Geneviève
Role of Caspase-10-P13tBID axis in erythropoiesis regulation
title Role of Caspase-10-P13tBID axis in erythropoiesis regulation
title_full Role of Caspase-10-P13tBID axis in erythropoiesis regulation
title_fullStr Role of Caspase-10-P13tBID axis in erythropoiesis regulation
title_full_unstemmed Role of Caspase-10-P13tBID axis in erythropoiesis regulation
title_short Role of Caspase-10-P13tBID axis in erythropoiesis regulation
title_sort role of caspase-10-p13tbid axis in erythropoiesis regulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9883265/
https://www.ncbi.nlm.nih.gov/pubmed/36202990
http://dx.doi.org/10.1038/s41418-022-01066-0
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