Cargando…

The HSPB1-p62/SQSTM1 functional complex regulates the unconventional secretion and transcellular spreading of the HD-associated mutant huntingtin protein

Conformational diseases, such as Alzheimer, Parkinson and Huntington diseases, are part of a common class of neurological disorders characterized by the aggregation and progressive accumulation of proteins bearing aberrant conformations. Huntington disease (HD) has autosomal dominant inheritance and...

Descripción completa

Detalles Bibliográficos
Autores principales: Bonavita, R, Scerra, G, Di Martino, R, Nuzzo, S, Polishchuk, E, Di Gennaro, M, Williams, S V, Caporaso, M G, Caiazza, C, Polishchuk, R, D’Agostino, M, Fleming, A, Renna, M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10321397/
https://www.ncbi.nlm.nih.gov/pubmed/36971475
http://dx.doi.org/10.1093/hmg/ddad047
_version_ 1785068611359997952
author Bonavita, R
Scerra, G
Di Martino, R
Nuzzo, S
Polishchuk, E
Di Gennaro, M
Williams, S V
Caporaso, M G
Caiazza, C
Polishchuk, R
D’Agostino, M
Fleming, A
Renna, M
author_facet Bonavita, R
Scerra, G
Di Martino, R
Nuzzo, S
Polishchuk, E
Di Gennaro, M
Williams, S V
Caporaso, M G
Caiazza, C
Polishchuk, R
D’Agostino, M
Fleming, A
Renna, M
author_sort Bonavita, R
collection PubMed
description Conformational diseases, such as Alzheimer, Parkinson and Huntington diseases, are part of a common class of neurological disorders characterized by the aggregation and progressive accumulation of proteins bearing aberrant conformations. Huntington disease (HD) has autosomal dominant inheritance and is caused by mutations leading to an abnormal expansion in the polyglutamine (polyQ) tract of the huntingtin (HTT) protein, leading to the formation of HTT inclusion bodies in neurons of affected patients. Interestingly, recent experimental evidence is challenging the conventional view by which the disease pathogenesis is solely a consequence of the intracellular accumulation of mutant protein aggregates. These studies reveal that transcellular transfer of mutated huntingtin protein is able to seed oligomers involving even the wild-type (WT) forms of the protein. To date, there is still no successful strategy to treat HD. Here, we describe a novel functional role for the HSPB1-p62/SQSTM1 complex, which acts as a cargo loading platform, allowing the unconventional secretion of mutant HTT by extracellular vesicles. HSPB1 interacts preferentially with polyQ-expanded HTT compared with the WT protein and affects its aggregation. Furthermore, HSPB1 levels correlate with the rate of mutant HTT secretion, which is controlled by the activity of the PI3K/AKT/mTOR signalling pathway. Finally, we show that these HTT-containing vesicular structures are biologically active and able to be internalized by recipient cells, therefore providing an additional mechanism to explain the prion-like spreading properties of mutant HTT. These findings might also have implications for the turn-over of other disease-associated, aggregation-prone proteins.
format Online
Article
Text
id pubmed-10321397
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-103213972023-07-06 The HSPB1-p62/SQSTM1 functional complex regulates the unconventional secretion and transcellular spreading of the HD-associated mutant huntingtin protein Bonavita, R Scerra, G Di Martino, R Nuzzo, S Polishchuk, E Di Gennaro, M Williams, S V Caporaso, M G Caiazza, C Polishchuk, R D’Agostino, M Fleming, A Renna, M Hum Mol Genet Original Article Conformational diseases, such as Alzheimer, Parkinson and Huntington diseases, are part of a common class of neurological disorders characterized by the aggregation and progressive accumulation of proteins bearing aberrant conformations. Huntington disease (HD) has autosomal dominant inheritance and is caused by mutations leading to an abnormal expansion in the polyglutamine (polyQ) tract of the huntingtin (HTT) protein, leading to the formation of HTT inclusion bodies in neurons of affected patients. Interestingly, recent experimental evidence is challenging the conventional view by which the disease pathogenesis is solely a consequence of the intracellular accumulation of mutant protein aggregates. These studies reveal that transcellular transfer of mutated huntingtin protein is able to seed oligomers involving even the wild-type (WT) forms of the protein. To date, there is still no successful strategy to treat HD. Here, we describe a novel functional role for the HSPB1-p62/SQSTM1 complex, which acts as a cargo loading platform, allowing the unconventional secretion of mutant HTT by extracellular vesicles. HSPB1 interacts preferentially with polyQ-expanded HTT compared with the WT protein and affects its aggregation. Furthermore, HSPB1 levels correlate with the rate of mutant HTT secretion, which is controlled by the activity of the PI3K/AKT/mTOR signalling pathway. Finally, we show that these HTT-containing vesicular structures are biologically active and able to be internalized by recipient cells, therefore providing an additional mechanism to explain the prion-like spreading properties of mutant HTT. These findings might also have implications for the turn-over of other disease-associated, aggregation-prone proteins. Oxford University Press 2023-03-27 /pmc/articles/PMC10321397/ /pubmed/36971475 http://dx.doi.org/10.1093/hmg/ddad047 Text en © The Author(s) 2023. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Bonavita, R
Scerra, G
Di Martino, R
Nuzzo, S
Polishchuk, E
Di Gennaro, M
Williams, S V
Caporaso, M G
Caiazza, C
Polishchuk, R
D’Agostino, M
Fleming, A
Renna, M
The HSPB1-p62/SQSTM1 functional complex regulates the unconventional secretion and transcellular spreading of the HD-associated mutant huntingtin protein
title The HSPB1-p62/SQSTM1 functional complex regulates the unconventional secretion and transcellular spreading of the HD-associated mutant huntingtin protein
title_full The HSPB1-p62/SQSTM1 functional complex regulates the unconventional secretion and transcellular spreading of the HD-associated mutant huntingtin protein
title_fullStr The HSPB1-p62/SQSTM1 functional complex regulates the unconventional secretion and transcellular spreading of the HD-associated mutant huntingtin protein
title_full_unstemmed The HSPB1-p62/SQSTM1 functional complex regulates the unconventional secretion and transcellular spreading of the HD-associated mutant huntingtin protein
title_short The HSPB1-p62/SQSTM1 functional complex regulates the unconventional secretion and transcellular spreading of the HD-associated mutant huntingtin protein
title_sort hspb1-p62/sqstm1 functional complex regulates the unconventional secretion and transcellular spreading of the hd-associated mutant huntingtin protein
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10321397/
https://www.ncbi.nlm.nih.gov/pubmed/36971475
http://dx.doi.org/10.1093/hmg/ddad047
work_keys_str_mv AT bonavitar thehspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT scerrag thehspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT dimartinor thehspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT nuzzos thehspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT polishchuke thehspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT digennarom thehspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT williamssv thehspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT caporasomg thehspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT caiazzac thehspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT polishchukr thehspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT dagostinom thehspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT fleminga thehspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT rennam thehspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT bonavitar hspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT scerrag hspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT dimartinor hspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT nuzzos hspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT polishchuke hspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT digennarom hspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT williamssv hspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT caporasomg hspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT caiazzac hspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT polishchukr hspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT dagostinom hspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT fleminga hspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein
AT rennam hspb1p62sqstm1functionalcomplexregulatestheunconventionalsecretionandtranscellularspreadingofthehdassociatedmutanthuntingtinprotein