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The Association between α-Synuclein and α-Tubulin in Brain Synapses
α-synuclein is a small protein that is mainly expressed in the synaptic terminals of nervous tissue. Although its implication in neurodegeneration is well established, the physiological role of α-synuclein remains elusive. Given its involvement in the modulation of synaptic transmission and the emer...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8430732/ https://www.ncbi.nlm.nih.gov/pubmed/34502063 http://dx.doi.org/10.3390/ijms22179153 |
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author | Amadeo, Alida Pizzi, Sara Comincini, Alessandro Modena, Debora Calogero, Alessandra Maria Madaschi, Laura Faustini, Gaia Rolando, Chiara Bellucci, Arianna Pezzoli, Gianni Mazzetti, Samanta Cappelletti, Graziella |
author_facet | Amadeo, Alida Pizzi, Sara Comincini, Alessandro Modena, Debora Calogero, Alessandra Maria Madaschi, Laura Faustini, Gaia Rolando, Chiara Bellucci, Arianna Pezzoli, Gianni Mazzetti, Samanta Cappelletti, Graziella |
author_sort | Amadeo, Alida |
collection | PubMed |
description | α-synuclein is a small protein that is mainly expressed in the synaptic terminals of nervous tissue. Although its implication in neurodegeneration is well established, the physiological role of α-synuclein remains elusive. Given its involvement in the modulation of synaptic transmission and the emerging role of microtubules at the synapse, the current study aimed at investigating whether α-synuclein becomes involved with this cytoskeletal component at the presynapse. We first analyzed the expression of α-synuclein and its colocalization with α-tubulin in murine brain. Differences were found between cortical and striatal/midbrain areas, with substantia nigra pars compacta and corpus striatum showing the lowest levels of colocalization. Using a proximity ligation assay, we revealed the direct interaction of α-synuclein with α-tubulin in murine and in human brain. Finally, the previously unexplored interaction of the two proteins in vivo at the synapse was disclosed in murine striatal presynaptic boutons through multiple approaches, from confocal spinning disk to electron microscopy. Collectively, our data strongly suggest that the association with tubulin/microtubules might actually be an important physiological function for α-synuclein in the synapse, thus suggesting its potential role in a neuropathological context. |
format | Online Article Text |
id | pubmed-8430732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84307322021-09-11 The Association between α-Synuclein and α-Tubulin in Brain Synapses Amadeo, Alida Pizzi, Sara Comincini, Alessandro Modena, Debora Calogero, Alessandra Maria Madaschi, Laura Faustini, Gaia Rolando, Chiara Bellucci, Arianna Pezzoli, Gianni Mazzetti, Samanta Cappelletti, Graziella Int J Mol Sci Article α-synuclein is a small protein that is mainly expressed in the synaptic terminals of nervous tissue. Although its implication in neurodegeneration is well established, the physiological role of α-synuclein remains elusive. Given its involvement in the modulation of synaptic transmission and the emerging role of microtubules at the synapse, the current study aimed at investigating whether α-synuclein becomes involved with this cytoskeletal component at the presynapse. We first analyzed the expression of α-synuclein and its colocalization with α-tubulin in murine brain. Differences were found between cortical and striatal/midbrain areas, with substantia nigra pars compacta and corpus striatum showing the lowest levels of colocalization. Using a proximity ligation assay, we revealed the direct interaction of α-synuclein with α-tubulin in murine and in human brain. Finally, the previously unexplored interaction of the two proteins in vivo at the synapse was disclosed in murine striatal presynaptic boutons through multiple approaches, from confocal spinning disk to electron microscopy. Collectively, our data strongly suggest that the association with tubulin/microtubules might actually be an important physiological function for α-synuclein in the synapse, thus suggesting its potential role in a neuropathological context. MDPI 2021-08-25 /pmc/articles/PMC8430732/ /pubmed/34502063 http://dx.doi.org/10.3390/ijms22179153 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Amadeo, Alida Pizzi, Sara Comincini, Alessandro Modena, Debora Calogero, Alessandra Maria Madaschi, Laura Faustini, Gaia Rolando, Chiara Bellucci, Arianna Pezzoli, Gianni Mazzetti, Samanta Cappelletti, Graziella The Association between α-Synuclein and α-Tubulin in Brain Synapses |
title | The Association between α-Synuclein and α-Tubulin in Brain Synapses |
title_full | The Association between α-Synuclein and α-Tubulin in Brain Synapses |
title_fullStr | The Association between α-Synuclein and α-Tubulin in Brain Synapses |
title_full_unstemmed | The Association between α-Synuclein and α-Tubulin in Brain Synapses |
title_short | The Association between α-Synuclein and α-Tubulin in Brain Synapses |
title_sort | association between α-synuclein and α-tubulin in brain synapses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8430732/ https://www.ncbi.nlm.nih.gov/pubmed/34502063 http://dx.doi.org/10.3390/ijms22179153 |
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