Cargando…

Organization of Presynaptic Autophagy-Related Processes

Brain synapses pose special challenges on the quality control of their protein machineries as they are far away from the neuronal soma, display a high potential for plastic adaptation and have a high energy demand to fulfill their physiological tasks. This applies in particular to the presynaptic pa...

Descripción completa

Detalles Bibliográficos
Autores principales: Gundelfinger, Eckart D., Karpova, Anna, Pielot, Rainer, Garner, Craig C., Kreutz, Michael R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968026/
https://www.ncbi.nlm.nih.gov/pubmed/35368245
http://dx.doi.org/10.3389/fnsyn.2022.829354
_version_ 1784678957931560960
author Gundelfinger, Eckart D.
Karpova, Anna
Pielot, Rainer
Garner, Craig C.
Kreutz, Michael R.
author_facet Gundelfinger, Eckart D.
Karpova, Anna
Pielot, Rainer
Garner, Craig C.
Kreutz, Michael R.
author_sort Gundelfinger, Eckart D.
collection PubMed
description Brain synapses pose special challenges on the quality control of their protein machineries as they are far away from the neuronal soma, display a high potential for plastic adaptation and have a high energy demand to fulfill their physiological tasks. This applies in particular to the presynaptic part where neurotransmitter is released from synaptic vesicles, which in turn have to be recycled and refilled in a complex membrane trafficking cycle. Pathways to remove outdated and damaged proteins include the ubiquitin-proteasome system acting in the cytoplasm as well as membrane-associated endolysosomal and the autophagy systems. Here we focus on the latter systems and review what is known about the spatial organization of autophagy and endolysomal processes within the presynapse. We provide an inventory of which components of these degradative systems were found to be present in presynaptic boutons and where they might be anchored to the presynaptic apparatus. We identify three presynaptic structures reported to interact with known constituents of membrane-based protein-degradation pathways and therefore may serve as docking stations. These are (i) scaffolding proteins of the cytomatrix at the active zone, such as Bassoon or Clarinet, (ii) the endocytic machinery localized mainly at the peri-active zone, and (iii) synaptic vesicles. Finally, we sketch scenarios, how presynaptic autophagic cargos are tagged and recruited and which cellular mechanisms may govern membrane-associated protein turnover in the presynapse.
format Online
Article
Text
id pubmed-8968026
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-89680262022-04-01 Organization of Presynaptic Autophagy-Related Processes Gundelfinger, Eckart D. Karpova, Anna Pielot, Rainer Garner, Craig C. Kreutz, Michael R. Front Synaptic Neurosci Neuroscience Brain synapses pose special challenges on the quality control of their protein machineries as they are far away from the neuronal soma, display a high potential for plastic adaptation and have a high energy demand to fulfill their physiological tasks. This applies in particular to the presynaptic part where neurotransmitter is released from synaptic vesicles, which in turn have to be recycled and refilled in a complex membrane trafficking cycle. Pathways to remove outdated and damaged proteins include the ubiquitin-proteasome system acting in the cytoplasm as well as membrane-associated endolysosomal and the autophagy systems. Here we focus on the latter systems and review what is known about the spatial organization of autophagy and endolysomal processes within the presynapse. We provide an inventory of which components of these degradative systems were found to be present in presynaptic boutons and where they might be anchored to the presynaptic apparatus. We identify three presynaptic structures reported to interact with known constituents of membrane-based protein-degradation pathways and therefore may serve as docking stations. These are (i) scaffolding proteins of the cytomatrix at the active zone, such as Bassoon or Clarinet, (ii) the endocytic machinery localized mainly at the peri-active zone, and (iii) synaptic vesicles. Finally, we sketch scenarios, how presynaptic autophagic cargos are tagged and recruited and which cellular mechanisms may govern membrane-associated protein turnover in the presynapse. Frontiers Media S.A. 2022-03-17 /pmc/articles/PMC8968026/ /pubmed/35368245 http://dx.doi.org/10.3389/fnsyn.2022.829354 Text en Copyright © 2022 Gundelfinger, Karpova, Pielot, Garner and Kreutz. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Gundelfinger, Eckart D.
Karpova, Anna
Pielot, Rainer
Garner, Craig C.
Kreutz, Michael R.
Organization of Presynaptic Autophagy-Related Processes
title Organization of Presynaptic Autophagy-Related Processes
title_full Organization of Presynaptic Autophagy-Related Processes
title_fullStr Organization of Presynaptic Autophagy-Related Processes
title_full_unstemmed Organization of Presynaptic Autophagy-Related Processes
title_short Organization of Presynaptic Autophagy-Related Processes
title_sort organization of presynaptic autophagy-related processes
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968026/
https://www.ncbi.nlm.nih.gov/pubmed/35368245
http://dx.doi.org/10.3389/fnsyn.2022.829354
work_keys_str_mv AT gundelfingereckartd organizationofpresynapticautophagyrelatedprocesses
AT karpovaanna organizationofpresynapticautophagyrelatedprocesses
AT pielotrainer organizationofpresynapticautophagyrelatedprocesses
AT garnercraigc organizationofpresynapticautophagyrelatedprocesses
AT kreutzmichaelr organizationofpresynapticautophagyrelatedprocesses