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Single-Nucleotide Polymorphism 309T>G in the MDM2 Promoter Determines Functional Outcome After Stroke

BACKGROUND AND PURPOSE—: The E3 ubiquitin ligase MDM2 (murine double minute 2) is the main negative regulator of the p53 protein—a key player in neuronal apoptosis after ischemia. A functional single-nucleotide polymorphism in the human MDM2 gene promoter (rs2279744) regulates MDM2 protein expressio...

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Autores principales: Rodríguez, Cristina, Ramos-Araque, María E., Domínguez-Martínez, Marta, Sobrino, Tomás, Sánchez-Morán, Irene, Agulla, Jesús, Delgado-Esteban, María, Gómez-Sánchez, José C., Bolaños, Juan P., Castillo, José, Almeida, Angeles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6159670/
https://www.ncbi.nlm.nih.gov/pubmed/30355102
http://dx.doi.org/10.1161/STROKEAHA.118.022529
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author Rodríguez, Cristina
Ramos-Araque, María E.
Domínguez-Martínez, Marta
Sobrino, Tomás
Sánchez-Morán, Irene
Agulla, Jesús
Delgado-Esteban, María
Gómez-Sánchez, José C.
Bolaños, Juan P.
Castillo, José
Almeida, Angeles
author_facet Rodríguez, Cristina
Ramos-Araque, María E.
Domínguez-Martínez, Marta
Sobrino, Tomás
Sánchez-Morán, Irene
Agulla, Jesús
Delgado-Esteban, María
Gómez-Sánchez, José C.
Bolaños, Juan P.
Castillo, José
Almeida, Angeles
author_sort Rodríguez, Cristina
collection PubMed
description BACKGROUND AND PURPOSE—: The E3 ubiquitin ligase MDM2 (murine double minute 2) is the main negative regulator of the p53 protein—a key player in neuronal apoptosis after ischemia. A functional single-nucleotide polymorphism in the human MDM2 gene promoter (rs2279744) regulates MDM2 protein expression. We investigated whether the MDM2 SNP309, by controlling p53-mediated apoptosis, determines functional outcome after stroke. METHODS—: Primary cortical neurons were subjected to oxygen and glucose deprivation. Mice were subjected to ischemic (transient middle cerebral artery occlusion) or hemorrhagic (collagenase injection) stroke models. Protein and mRNA levels of MDM2 and p53 were measured in both neuronal and brain extracts. The interaction of MDM2 with p53 was disrupted by neuronal treatment with nutlin-3a. siRNA was used to knockdown MDM2 expression. We analyzed the link between the MDM2 SNP309 and functional outcome, measured by the modified Rankin Scale scores, in 2 independent hospital-based stroke cohorts: ischemic stroke cohort (408 patients) and intracerebral hemorrhage cohort (128 patients). RESULTS—: Experimental stroke and oxygen and glucose deprivation induced the expression of MDM2 in the brain and neurons, respectively. Moreover, oxygen and glucose deprivation promoted MDM2 binding with p53 in neurons. Disruption of the MDM2-p53 interaction with nutlin-3a, or MDM2 knockdown by siRNA, triggered p53 accumulation, which increased neuronal susceptibility to oxygen and glucose deprivation-induced apoptosis. Finally, we showed that patients harboring the G allele in the MDM2 promoter had higher MDM2 protein levels and showed better functional outcome after stroke than those harboring the T/T genotype. The T/T genotype was also associated with large infarct volume in ischemic stroke and increased lesion volume in patients with intracerebral hemorrhage. CONCLUSIONS—: Our results reveal a novel role for the MDM2-p53 interaction in neuronal apoptosis after ischemia and show that the MDM2 SNP309 determines the functional outcome of patients after stroke.
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spelling pubmed-61596702018-10-12 Single-Nucleotide Polymorphism 309T>G in the MDM2 Promoter Determines Functional Outcome After Stroke Rodríguez, Cristina Ramos-Araque, María E. Domínguez-Martínez, Marta Sobrino, Tomás Sánchez-Morán, Irene Agulla, Jesús Delgado-Esteban, María Gómez-Sánchez, José C. Bolaños, Juan P. Castillo, José Almeida, Angeles Stroke Original Contributions BACKGROUND AND PURPOSE—: The E3 ubiquitin ligase MDM2 (murine double minute 2) is the main negative regulator of the p53 protein—a key player in neuronal apoptosis after ischemia. A functional single-nucleotide polymorphism in the human MDM2 gene promoter (rs2279744) regulates MDM2 protein expression. We investigated whether the MDM2 SNP309, by controlling p53-mediated apoptosis, determines functional outcome after stroke. METHODS—: Primary cortical neurons were subjected to oxygen and glucose deprivation. Mice were subjected to ischemic (transient middle cerebral artery occlusion) or hemorrhagic (collagenase injection) stroke models. Protein and mRNA levels of MDM2 and p53 were measured in both neuronal and brain extracts. The interaction of MDM2 with p53 was disrupted by neuronal treatment with nutlin-3a. siRNA was used to knockdown MDM2 expression. We analyzed the link between the MDM2 SNP309 and functional outcome, measured by the modified Rankin Scale scores, in 2 independent hospital-based stroke cohorts: ischemic stroke cohort (408 patients) and intracerebral hemorrhage cohort (128 patients). RESULTS—: Experimental stroke and oxygen and glucose deprivation induced the expression of MDM2 in the brain and neurons, respectively. Moreover, oxygen and glucose deprivation promoted MDM2 binding with p53 in neurons. Disruption of the MDM2-p53 interaction with nutlin-3a, or MDM2 knockdown by siRNA, triggered p53 accumulation, which increased neuronal susceptibility to oxygen and glucose deprivation-induced apoptosis. Finally, we showed that patients harboring the G allele in the MDM2 promoter had higher MDM2 protein levels and showed better functional outcome after stroke than those harboring the T/T genotype. The T/T genotype was also associated with large infarct volume in ischemic stroke and increased lesion volume in patients with intracerebral hemorrhage. CONCLUSIONS—: Our results reveal a novel role for the MDM2-p53 interaction in neuronal apoptosis after ischemia and show that the MDM2 SNP309 determines the functional outcome of patients after stroke. Lippincott Williams & Wilkins 2018-10 2018-08-30 /pmc/articles/PMC6159670/ /pubmed/30355102 http://dx.doi.org/10.1161/STROKEAHA.118.022529 Text en © 2018 The Authors. Stroke is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial-NoDerivs (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited, the use is noncommercial, and no modifications or adaptations are made.
spellingShingle Original Contributions
Rodríguez, Cristina
Ramos-Araque, María E.
Domínguez-Martínez, Marta
Sobrino, Tomás
Sánchez-Morán, Irene
Agulla, Jesús
Delgado-Esteban, María
Gómez-Sánchez, José C.
Bolaños, Juan P.
Castillo, José
Almeida, Angeles
Single-Nucleotide Polymorphism 309T>G in the MDM2 Promoter Determines Functional Outcome After Stroke
title Single-Nucleotide Polymorphism 309T>G in the MDM2 Promoter Determines Functional Outcome After Stroke
title_full Single-Nucleotide Polymorphism 309T>G in the MDM2 Promoter Determines Functional Outcome After Stroke
title_fullStr Single-Nucleotide Polymorphism 309T>G in the MDM2 Promoter Determines Functional Outcome After Stroke
title_full_unstemmed Single-Nucleotide Polymorphism 309T>G in the MDM2 Promoter Determines Functional Outcome After Stroke
title_short Single-Nucleotide Polymorphism 309T>G in the MDM2 Promoter Determines Functional Outcome After Stroke
title_sort single-nucleotide polymorphism 309t>g in the mdm2 promoter determines functional outcome after stroke
topic Original Contributions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6159670/
https://www.ncbi.nlm.nih.gov/pubmed/30355102
http://dx.doi.org/10.1161/STROKEAHA.118.022529
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