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HuR (Elavl1) and HuB (Elavl2) Stabilize Matrix Metalloproteinase-9 mRNA During Seizure-Induced Mmp-9 Expression in Neurons

Matrix metalloproteinase-9 (Mmp-9) is involved in different general and cell-type–specific processes, both in neuronal and non-neuronal cells. Moreover, it is implicated in an induction or progression of various human disorders, including diseases of the central nervous system. Mechanisms regulating...

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Autores principales: Zybura-Broda, Katarzyna, Wolder-Gontarek, Malgorzata, Ambrozek-Latecka, Magdalena, Choros, Artur, Bogusz, Agnieszka, Wilemska-Dziaduszycka, Joanna, Rylski, Marcin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5900018/
https://www.ncbi.nlm.nih.gov/pubmed/29686606
http://dx.doi.org/10.3389/fnins.2018.00224
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author Zybura-Broda, Katarzyna
Wolder-Gontarek, Malgorzata
Ambrozek-Latecka, Magdalena
Choros, Artur
Bogusz, Agnieszka
Wilemska-Dziaduszycka, Joanna
Rylski, Marcin
author_facet Zybura-Broda, Katarzyna
Wolder-Gontarek, Malgorzata
Ambrozek-Latecka, Magdalena
Choros, Artur
Bogusz, Agnieszka
Wilemska-Dziaduszycka, Joanna
Rylski, Marcin
author_sort Zybura-Broda, Katarzyna
collection PubMed
description Matrix metalloproteinase-9 (Mmp-9) is involved in different general and cell-type–specific processes, both in neuronal and non-neuronal cells. Moreover, it is implicated in an induction or progression of various human disorders, including diseases of the central nervous system. Mechanisms regulating activity-driven Mmp-9 expression in neurons are still not fully understood. Here, we show that stabilization of Mmp-9 mRNA is one of the factors responsible for the neuronal activity-evoked upregulation of Mmp-9 mRNA expression in hippocampal neurons. Furthermore, we demonstrate that the molecular mechanism related to this stabilization is dependent on the neuronal seizure-triggered transiently increased binding of the mRNA stability-inducing protein, HuR, to ARE1 and ARE4 motifs of the 3′UTR for Mmp-9 mRNA as well as the stably augmented association of another mRNA-stabilizing protein, HuB, to the ARE1 element of the 3′UTR. Intriguingly, we demonstrate further that both HuR and HuB are crucial for an incidence of Mmp-9 mRNA stabilization after neuronal activation. This study identifies Mmp-9 mRNA as the first HuB target regulated by mRNA stabilization in neurons. Moreover, these results are the first to describe an existence of HuR-dependent mRNA stabilization in neurons of the brain.
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spelling pubmed-59000182018-04-23 HuR (Elavl1) and HuB (Elavl2) Stabilize Matrix Metalloproteinase-9 mRNA During Seizure-Induced Mmp-9 Expression in Neurons Zybura-Broda, Katarzyna Wolder-Gontarek, Malgorzata Ambrozek-Latecka, Magdalena Choros, Artur Bogusz, Agnieszka Wilemska-Dziaduszycka, Joanna Rylski, Marcin Front Neurosci Neuroscience Matrix metalloproteinase-9 (Mmp-9) is involved in different general and cell-type–specific processes, both in neuronal and non-neuronal cells. Moreover, it is implicated in an induction or progression of various human disorders, including diseases of the central nervous system. Mechanisms regulating activity-driven Mmp-9 expression in neurons are still not fully understood. Here, we show that stabilization of Mmp-9 mRNA is one of the factors responsible for the neuronal activity-evoked upregulation of Mmp-9 mRNA expression in hippocampal neurons. Furthermore, we demonstrate that the molecular mechanism related to this stabilization is dependent on the neuronal seizure-triggered transiently increased binding of the mRNA stability-inducing protein, HuR, to ARE1 and ARE4 motifs of the 3′UTR for Mmp-9 mRNA as well as the stably augmented association of another mRNA-stabilizing protein, HuB, to the ARE1 element of the 3′UTR. Intriguingly, we demonstrate further that both HuR and HuB are crucial for an incidence of Mmp-9 mRNA stabilization after neuronal activation. This study identifies Mmp-9 mRNA as the first HuB target regulated by mRNA stabilization in neurons. Moreover, these results are the first to describe an existence of HuR-dependent mRNA stabilization in neurons of the brain. Frontiers Media S.A. 2018-04-09 /pmc/articles/PMC5900018/ /pubmed/29686606 http://dx.doi.org/10.3389/fnins.2018.00224 Text en Copyright © 2018 Zybura-Broda, Wolder-Gontarek, Ambrozek-Latecka, Choros, Bogusz, Wilemska-Dziaduszycka and Rylski. http://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 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 Neuroscience
Zybura-Broda, Katarzyna
Wolder-Gontarek, Malgorzata
Ambrozek-Latecka, Magdalena
Choros, Artur
Bogusz, Agnieszka
Wilemska-Dziaduszycka, Joanna
Rylski, Marcin
HuR (Elavl1) and HuB (Elavl2) Stabilize Matrix Metalloproteinase-9 mRNA During Seizure-Induced Mmp-9 Expression in Neurons
title HuR (Elavl1) and HuB (Elavl2) Stabilize Matrix Metalloproteinase-9 mRNA During Seizure-Induced Mmp-9 Expression in Neurons
title_full HuR (Elavl1) and HuB (Elavl2) Stabilize Matrix Metalloproteinase-9 mRNA During Seizure-Induced Mmp-9 Expression in Neurons
title_fullStr HuR (Elavl1) and HuB (Elavl2) Stabilize Matrix Metalloproteinase-9 mRNA During Seizure-Induced Mmp-9 Expression in Neurons
title_full_unstemmed HuR (Elavl1) and HuB (Elavl2) Stabilize Matrix Metalloproteinase-9 mRNA During Seizure-Induced Mmp-9 Expression in Neurons
title_short HuR (Elavl1) and HuB (Elavl2) Stabilize Matrix Metalloproteinase-9 mRNA During Seizure-Induced Mmp-9 Expression in Neurons
title_sort hur (elavl1) and hub (elavl2) stabilize matrix metalloproteinase-9 mrna during seizure-induced mmp-9 expression in neurons
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5900018/
https://www.ncbi.nlm.nih.gov/pubmed/29686606
http://dx.doi.org/10.3389/fnins.2018.00224
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