Evidence map›Paper›PMID 35368245›Full record

ReviewFrontiers in synaptic neuroscience2022

Organization of Presynaptic Autophagy-Related Processes.

Eckart D Gundelfinger, Anna Karpova, Rainer Pielot, Craig C Garner, Michael R Kreutz

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in synaptic neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.1field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Oxysterols in Central and Peripheral Synaptic Communication.Advances in experimental medicine and biology · 2024
    Article
  6. Article
  7. Article
  8. S-SCAM is essential for synapse formation.Frontiers in cellular neuroscience · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 1 country.

Eckart D GundelfingerResearch Group Neuroplasticity, Leibniz Institute for Neurobiology, Magdeburg, Germany.
Anna KarpovaResearch Group Neuroplasticity, Leibniz Institute for Neurobiology, Magdeburg, Germany.
Rainer PielotInstitute of Pharmacology and Toxicology, Medical Faculty, Otto von Guericke University, Magdeburg, Germany.
Craig C GarnerGerman Center for Neurodegenerative Diseases (DZNE), Berlin, Germany.
Michael R KreutzResearch Group Neuroplasticity, Leibniz Institute for Neurobiology, Magdeburg, Germany.
Leibniz Institute for Neurobiology · DECenter for Behavioral Brain Sciences · DEGerman Center for Neurodegenerative Diseases · DEUniversity Medical Center Hamburg-Eppendorf · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

active zone (AZ)amphisomeautophagyBassoonendocytic zoneendolysosomal systempresynaptic proteostasissynaptic vesicle (SV)

Identifiers

PMID35368245
PMCPMC8968026
OpenAlexW4221021485

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.