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Cystatin B Involvement in Synapse Physiology of Rodent Brains and Human Cerebral Organoids
Cystatin B (CSTB) is a ubiquitous protein belonging to a superfamily of protease inhibitors. CSTB may play a critical role in brain physiology because its mutations cause progressive myoclonic epilepsy-1A (EPM1A), the most common form of progressive myoclonic epilepsy. However, the molecular mechani...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707391/ https://www.ncbi.nlm.nih.gov/pubmed/31467503 http://dx.doi.org/10.3389/fnmol.2019.00195 |
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author | Penna, Eduardo Cerciello, Angela Chambery, Angela Russo, Rosita Cernilogar, Filippo M. Pedone, Emilia Maria Perrone-Capano, Carla Cappello, Silvia Di Giaimo, Rossella Crispino, Marianna |
author_facet | Penna, Eduardo Cerciello, Angela Chambery, Angela Russo, Rosita Cernilogar, Filippo M. Pedone, Emilia Maria Perrone-Capano, Carla Cappello, Silvia Di Giaimo, Rossella Crispino, Marianna |
author_sort | Penna, Eduardo |
collection | PubMed |
description | Cystatin B (CSTB) is a ubiquitous protein belonging to a superfamily of protease inhibitors. CSTB may play a critical role in brain physiology because its mutations cause progressive myoclonic epilepsy-1A (EPM1A), the most common form of progressive myoclonic epilepsy. However, the molecular mechanisms underlying the role of CSTB in the central nervous system (CNS) are largely unknown. To investigate the possible involvement of CSTB in the synaptic plasticity, we analyzed its expression in synaptosomes as a model system in studying the physiology of the synaptic regions of the CNS. We found that CSTB is not only present in the synaptosomes isolated from rat and mouse brain cortex, but also secreted into the medium in a depolarization-controlled manner. In addition, using biorthogonal noncanonical amino acid tagging (BONCAT) procedure, we demonstrated, for the first time, that CSTB is locally synthesized in the synaptosomes. The synaptic localization of CSTB was confirmed in a human 3D model of cortical development, namely cerebral organoids. Altogether, these results suggest that CSTB may play a role in the brain plasticity and open a new perspective in studying the involvement of CSTB deregulation in neurodegenerative and neuropsychiatric diseases. |
format | Online Article Text |
id | pubmed-6707391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67073912019-08-29 Cystatin B Involvement in Synapse Physiology of Rodent Brains and Human Cerebral Organoids Penna, Eduardo Cerciello, Angela Chambery, Angela Russo, Rosita Cernilogar, Filippo M. Pedone, Emilia Maria Perrone-Capano, Carla Cappello, Silvia Di Giaimo, Rossella Crispino, Marianna Front Mol Neurosci Neuroscience Cystatin B (CSTB) is a ubiquitous protein belonging to a superfamily of protease inhibitors. CSTB may play a critical role in brain physiology because its mutations cause progressive myoclonic epilepsy-1A (EPM1A), the most common form of progressive myoclonic epilepsy. However, the molecular mechanisms underlying the role of CSTB in the central nervous system (CNS) are largely unknown. To investigate the possible involvement of CSTB in the synaptic plasticity, we analyzed its expression in synaptosomes as a model system in studying the physiology of the synaptic regions of the CNS. We found that CSTB is not only present in the synaptosomes isolated from rat and mouse brain cortex, but also secreted into the medium in a depolarization-controlled manner. In addition, using biorthogonal noncanonical amino acid tagging (BONCAT) procedure, we demonstrated, for the first time, that CSTB is locally synthesized in the synaptosomes. The synaptic localization of CSTB was confirmed in a human 3D model of cortical development, namely cerebral organoids. Altogether, these results suggest that CSTB may play a role in the brain plasticity and open a new perspective in studying the involvement of CSTB deregulation in neurodegenerative and neuropsychiatric diseases. Frontiers Media S.A. 2019-08-16 /pmc/articles/PMC6707391/ /pubmed/31467503 http://dx.doi.org/10.3389/fnmol.2019.00195 Text en Copyright © 2019 Penna, Cerciello, Chambery, Russo, Cernilogar, Pedone, Perrone-Capano, Cappello, Di Giaimo and Crispino. 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(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 | Neuroscience Penna, Eduardo Cerciello, Angela Chambery, Angela Russo, Rosita Cernilogar, Filippo M. Pedone, Emilia Maria Perrone-Capano, Carla Cappello, Silvia Di Giaimo, Rossella Crispino, Marianna Cystatin B Involvement in Synapse Physiology of Rodent Brains and Human Cerebral Organoids |
title | Cystatin B Involvement in Synapse Physiology of Rodent Brains and Human Cerebral Organoids |
title_full | Cystatin B Involvement in Synapse Physiology of Rodent Brains and Human Cerebral Organoids |
title_fullStr | Cystatin B Involvement in Synapse Physiology of Rodent Brains and Human Cerebral Organoids |
title_full_unstemmed | Cystatin B Involvement in Synapse Physiology of Rodent Brains and Human Cerebral Organoids |
title_short | Cystatin B Involvement in Synapse Physiology of Rodent Brains and Human Cerebral Organoids |
title_sort | cystatin b involvement in synapse physiology of rodent brains and human cerebral organoids |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707391/ https://www.ncbi.nlm.nih.gov/pubmed/31467503 http://dx.doi.org/10.3389/fnmol.2019.00195 |
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