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Dynamics of the mouse brain cortical synaptic proteome during postnatal brain development
Development of the brain involves the formation and maturation of numerous synapses. This process requires prominent changes of the synaptic proteome and potentially involves thousands of different proteins at every synapse. To date the proteome analysis of synapse development has been studied spars...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066275/ https://www.ncbi.nlm.nih.gov/pubmed/27748445 http://dx.doi.org/10.1038/srep35456 |
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author | Gonzalez-Lozano, Miguel A. Klemmer, Patricia Gebuis, Titia Hassan, Chopie van Nierop, Pim van Kesteren, Ronald E. Smit, August B. Li, Ka Wan |
author_facet | Gonzalez-Lozano, Miguel A. Klemmer, Patricia Gebuis, Titia Hassan, Chopie van Nierop, Pim van Kesteren, Ronald E. Smit, August B. Li, Ka Wan |
author_sort | Gonzalez-Lozano, Miguel A. |
collection | PubMed |
description | Development of the brain involves the formation and maturation of numerous synapses. This process requires prominent changes of the synaptic proteome and potentially involves thousands of different proteins at every synapse. To date the proteome analysis of synapse development has been studied sparsely. Here, we analyzed the cortical synaptic membrane proteome of juvenile postnatal days 9 (P9), P15, P21, P27, adolescent (P35) and different adult ages P70, P140 and P280 of C57Bl6/J mice. Using a quantitative proteomics workflow we quantified 1560 proteins of which 696 showed statistically significant differences over time. Synaptic proteins generally showed increased levels during maturation, whereas proteins involved in protein synthesis generally decreased in abundance. In several cases, proteins from a single functional molecular entity, e.g., subunits of the NMDA receptor, showed differences in their temporal regulation, which may reflect specific synaptic development features of connectivity, strength and plasticity. SNARE proteins, Snap 29/47 and Stx 7/8/12, showed higher expression in immature animals. Finally, we evaluated the function of Cxadr that showed high expression levels at P9 and a fast decline in expression during neuronal development. Knock down of the expression of Cxadr in cultured primary mouse neurons revealed a significant decrease in synapse density. |
format | Online Article Text |
id | pubmed-5066275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50662752016-10-26 Dynamics of the mouse brain cortical synaptic proteome during postnatal brain development Gonzalez-Lozano, Miguel A. Klemmer, Patricia Gebuis, Titia Hassan, Chopie van Nierop, Pim van Kesteren, Ronald E. Smit, August B. Li, Ka Wan Sci Rep Article Development of the brain involves the formation and maturation of numerous synapses. This process requires prominent changes of the synaptic proteome and potentially involves thousands of different proteins at every synapse. To date the proteome analysis of synapse development has been studied sparsely. Here, we analyzed the cortical synaptic membrane proteome of juvenile postnatal days 9 (P9), P15, P21, P27, adolescent (P35) and different adult ages P70, P140 and P280 of C57Bl6/J mice. Using a quantitative proteomics workflow we quantified 1560 proteins of which 696 showed statistically significant differences over time. Synaptic proteins generally showed increased levels during maturation, whereas proteins involved in protein synthesis generally decreased in abundance. In several cases, proteins from a single functional molecular entity, e.g., subunits of the NMDA receptor, showed differences in their temporal regulation, which may reflect specific synaptic development features of connectivity, strength and plasticity. SNARE proteins, Snap 29/47 and Stx 7/8/12, showed higher expression in immature animals. Finally, we evaluated the function of Cxadr that showed high expression levels at P9 and a fast decline in expression during neuronal development. Knock down of the expression of Cxadr in cultured primary mouse neurons revealed a significant decrease in synapse density. Nature Publishing Group 2016-10-17 /pmc/articles/PMC5066275/ /pubmed/27748445 http://dx.doi.org/10.1038/srep35456 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Gonzalez-Lozano, Miguel A. Klemmer, Patricia Gebuis, Titia Hassan, Chopie van Nierop, Pim van Kesteren, Ronald E. Smit, August B. Li, Ka Wan Dynamics of the mouse brain cortical synaptic proteome during postnatal brain development |
title | Dynamics of the mouse brain cortical synaptic proteome during postnatal brain development |
title_full | Dynamics of the mouse brain cortical synaptic proteome during postnatal brain development |
title_fullStr | Dynamics of the mouse brain cortical synaptic proteome during postnatal brain development |
title_full_unstemmed | Dynamics of the mouse brain cortical synaptic proteome during postnatal brain development |
title_short | Dynamics of the mouse brain cortical synaptic proteome during postnatal brain development |
title_sort | dynamics of the mouse brain cortical synaptic proteome during postnatal brain development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066275/ https://www.ncbi.nlm.nih.gov/pubmed/27748445 http://dx.doi.org/10.1038/srep35456 |
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