Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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
_version_ 1783750772634157056
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
work_keys_str_mv AT amadeoalida theassociationbetweenasynucleinandatubulininbrainsynapses
AT pizzisara theassociationbetweenasynucleinandatubulininbrainsynapses
AT comincinialessandro theassociationbetweenasynucleinandatubulininbrainsynapses
AT modenadebora theassociationbetweenasynucleinandatubulininbrainsynapses
AT calogeroalessandramaria theassociationbetweenasynucleinandatubulininbrainsynapses
AT madaschilaura theassociationbetweenasynucleinandatubulininbrainsynapses
AT faustinigaia theassociationbetweenasynucleinandatubulininbrainsynapses
AT rolandochiara theassociationbetweenasynucleinandatubulininbrainsynapses
AT bellucciarianna theassociationbetweenasynucleinandatubulininbrainsynapses
AT pezzoligianni theassociationbetweenasynucleinandatubulininbrainsynapses
AT mazzettisamanta theassociationbetweenasynucleinandatubulininbrainsynapses
AT cappellettigraziella theassociationbetweenasynucleinandatubulininbrainsynapses
AT amadeoalida associationbetweenasynucleinandatubulininbrainsynapses
AT pizzisara associationbetweenasynucleinandatubulininbrainsynapses
AT comincinialessandro associationbetweenasynucleinandatubulininbrainsynapses
AT modenadebora associationbetweenasynucleinandatubulininbrainsynapses
AT calogeroalessandramaria associationbetweenasynucleinandatubulininbrainsynapses
AT madaschilaura associationbetweenasynucleinandatubulininbrainsynapses
AT faustinigaia associationbetweenasynucleinandatubulininbrainsynapses
AT rolandochiara associationbetweenasynucleinandatubulininbrainsynapses
AT bellucciarianna associationbetweenasynucleinandatubulininbrainsynapses
AT pezzoligianni associationbetweenasynucleinandatubulininbrainsynapses
AT mazzettisamanta associationbetweenasynucleinandatubulininbrainsynapses
AT cappellettigraziella associationbetweenasynucleinandatubulininbrainsynapses