Fast axonal transport of the proteasome complex depends on membrane interaction and molecular motor function
Protein degradation by the ubiquitin-proteasome system in neurons depends on the correct delivery of the proteasome complex. In neurodegenerative diseases, aggregation and accumulation of proteins in axons link transport defects with degradation impairments; however, the transport properties of prot...
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2014
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Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00219533_v127_n7_p1537_Otero http://hdl.handle.net/20.500.12110/paper_00219533_v127_n7_p1537_Otero |
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paper:paper_00219533_v127_n7_p1537_Otero2023-06-08T14:43:45Z Fast axonal transport of the proteasome complex depends on membrane interaction and molecular motor function Cromberg, Lucas Eneas Bruno, Luciana Falzone, Tomás Luis Axonal transport Kinesin-1 Membrane interaction Molecular motors Proteasome Vesicles molecular motor proteasome ubiquitin proteasome animal tissue article axoneme clearance controlled study degenerative disease diffusion Golgi complex in vivo study intracellular membrane lysosome mitochondrion molecular interaction motor unit mouse nerve fiber transport nonhuman priority journal protein degradation synapse vesicle viscoelasticity animal C57BL mouse cell culture cytology hippocampus intracellular membrane metabolism nerve fiber nerve fiber transport physiology sciatic nerve synaptosome transport at the cellular level Animals Axonal Transport Axons Biological Transport Cells, Cultured Hippocampus Intracellular Membranes Mice Mice, Inbred C57BL Proteasome Endopeptidase Complex Sciatic Nerve Synaptic Vesicles Synaptosomes Protein degradation by the ubiquitin-proteasome system in neurons depends on the correct delivery of the proteasome complex. In neurodegenerative diseases, aggregation and accumulation of proteins in axons link transport defects with degradation impairments; however, the transport properties of proteasomes remain unknown. Here, using in vivo experiments, we reveal the fast anterograde transport of assembled and functional 26S proteasome complexes. A high-resolution tracking system to follow fluorescent proteasomes revealed three types of motion: actively driven proteasome axonal transport, diffusive behavior in a viscoelastic axonema and proteasome-confined motion. We show that active proteasome transport depends on motor function because knockdown of the KIF5B motor subunit resulted in impairment of the anterograde proteasome flux and the density of segmental velocities. Finally, we reveal that neuronal proteasomes interact with intracellular membranes and identify the coordinated transport of fluorescent proteasomes with synaptic precursor vesicles, Golgi-derived vesicles, lysosomes and mitochondria. Taken together, our results reveal fast axonal transport as a new mechanism of proteasome delivery that depends on membrane cargo 'hitch-hiking' and the function of molecular motors. We further hypothesize that defects in proteasome transport could promote abnormal protein clearance in neurodegenerative diseases. © 2014.Published by The Company of Biologists Ltd. Fil:Cromberg, L.E. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Bruno, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Falzone, T.L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2014 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00219533_v127_n7_p1537_Otero http://hdl.handle.net/20.500.12110/paper_00219533_v127_n7_p1537_Otero |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
Axonal transport Kinesin-1 Membrane interaction Molecular motors Proteasome Vesicles molecular motor proteasome ubiquitin proteasome animal tissue article axoneme clearance controlled study degenerative disease diffusion Golgi complex in vivo study intracellular membrane lysosome mitochondrion molecular interaction motor unit mouse nerve fiber transport nonhuman priority journal protein degradation synapse vesicle viscoelasticity animal C57BL mouse cell culture cytology hippocampus intracellular membrane metabolism nerve fiber nerve fiber transport physiology sciatic nerve synaptosome transport at the cellular level Animals Axonal Transport Axons Biological Transport Cells, Cultured Hippocampus Intracellular Membranes Mice Mice, Inbred C57BL Proteasome Endopeptidase Complex Sciatic Nerve Synaptic Vesicles Synaptosomes |
spellingShingle |
Axonal transport Kinesin-1 Membrane interaction Molecular motors Proteasome Vesicles molecular motor proteasome ubiquitin proteasome animal tissue article axoneme clearance controlled study degenerative disease diffusion Golgi complex in vivo study intracellular membrane lysosome mitochondrion molecular interaction motor unit mouse nerve fiber transport nonhuman priority journal protein degradation synapse vesicle viscoelasticity animal C57BL mouse cell culture cytology hippocampus intracellular membrane metabolism nerve fiber nerve fiber transport physiology sciatic nerve synaptosome transport at the cellular level Animals Axonal Transport Axons Biological Transport Cells, Cultured Hippocampus Intracellular Membranes Mice Mice, Inbred C57BL Proteasome Endopeptidase Complex Sciatic Nerve Synaptic Vesicles Synaptosomes Cromberg, Lucas Eneas Bruno, Luciana Falzone, Tomás Luis Fast axonal transport of the proteasome complex depends on membrane interaction and molecular motor function |
topic_facet |
Axonal transport Kinesin-1 Membrane interaction Molecular motors Proteasome Vesicles molecular motor proteasome ubiquitin proteasome animal tissue article axoneme clearance controlled study degenerative disease diffusion Golgi complex in vivo study intracellular membrane lysosome mitochondrion molecular interaction motor unit mouse nerve fiber transport nonhuman priority journal protein degradation synapse vesicle viscoelasticity animal C57BL mouse cell culture cytology hippocampus intracellular membrane metabolism nerve fiber nerve fiber transport physiology sciatic nerve synaptosome transport at the cellular level Animals Axonal Transport Axons Biological Transport Cells, Cultured Hippocampus Intracellular Membranes Mice Mice, Inbred C57BL Proteasome Endopeptidase Complex Sciatic Nerve Synaptic Vesicles Synaptosomes |
description |
Protein degradation by the ubiquitin-proteasome system in neurons depends on the correct delivery of the proteasome complex. In neurodegenerative diseases, aggregation and accumulation of proteins in axons link transport defects with degradation impairments; however, the transport properties of proteasomes remain unknown. Here, using in vivo experiments, we reveal the fast anterograde transport of assembled and functional 26S proteasome complexes. A high-resolution tracking system to follow fluorescent proteasomes revealed three types of motion: actively driven proteasome axonal transport, diffusive behavior in a viscoelastic axonema and proteasome-confined motion. We show that active proteasome transport depends on motor function because knockdown of the KIF5B motor subunit resulted in impairment of the anterograde proteasome flux and the density of segmental velocities. Finally, we reveal that neuronal proteasomes interact with intracellular membranes and identify the coordinated transport of fluorescent proteasomes with synaptic precursor vesicles, Golgi-derived vesicles, lysosomes and mitochondria. Taken together, our results reveal fast axonal transport as a new mechanism of proteasome delivery that depends on membrane cargo 'hitch-hiking' and the function of molecular motors. We further hypothesize that defects in proteasome transport could promote abnormal protein clearance in neurodegenerative diseases. © 2014.Published by The Company of Biologists Ltd. |
author |
Cromberg, Lucas Eneas Bruno, Luciana Falzone, Tomás Luis |
author_facet |
Cromberg, Lucas Eneas Bruno, Luciana Falzone, Tomás Luis |
author_sort |
Cromberg, Lucas Eneas |
title |
Fast axonal transport of the proteasome complex depends on membrane interaction and molecular motor function |
title_short |
Fast axonal transport of the proteasome complex depends on membrane interaction and molecular motor function |
title_full |
Fast axonal transport of the proteasome complex depends on membrane interaction and molecular motor function |
title_fullStr |
Fast axonal transport of the proteasome complex depends on membrane interaction and molecular motor function |
title_full_unstemmed |
Fast axonal transport of the proteasome complex depends on membrane interaction and molecular motor function |
title_sort |
fast axonal transport of the proteasome complex depends on membrane interaction and molecular motor function |
publishDate |
2014 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00219533_v127_n7_p1537_Otero http://hdl.handle.net/20.500.12110/paper_00219533_v127_n7_p1537_Otero |
work_keys_str_mv |
AT cromberglucaseneas fastaxonaltransportoftheproteasomecomplexdependsonmembraneinteractionandmolecularmotorfunction AT brunoluciana fastaxonaltransportoftheproteasomecomplexdependsonmembraneinteractionandmolecularmotorfunction AT falzonetomasluis fastaxonaltransportoftheproteasomecomplexdependsonmembraneinteractionandmolecularmotorfunction |
_version_ |
1768544987087110144 |