Evidence map›Paper›PMID 36594894›Full record

ArticleThe Journal of comparative neurology2023

Neurodegeneration in a novel invertebrate model system: Failed microtubule-mediated cell adhesion and unraveling of macroglia.

Ruth Fabian-Fine, Anna M Aiken, Julia R Aug, Jason D Boucher, Danielle C Butler, Liam J Clancy, Shaun A Clem, Samantha C Crotty, Abigail M Dalpe, Elizabeth J Donzello-Jewett and 18 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

28 authors at 1 institution in 1 country.

Ruth Fabian-FineDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Anna M AikenDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Julia R AugDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Jason D BoucherDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Danielle C ButlerDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Liam J ClancyDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Shaun A ClemDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Samantha C CrottyDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Abigail M DalpeDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Elizabeth J Donzello-JewettDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Taylor M GalgayDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Bonnie K GillisDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Brigid W HeinrichDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Kai R HinesDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Jordan E KimmelDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Joseph M McGrathDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Marissa M MilesDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Jordyn A MoreyDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Isaiah A OrtizDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Kevin Q PhamDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Liam C QuinnDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Colin J RadicanDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Nolan T SpeidelDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Bailey J ThomasDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Angela R TroisiDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Joshua L WeissDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Kayne V WentzheimerDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.
Adam L WeaverDepartment of Biology and Neuroscience, Saint Michael's College, Colchester, Vermont, USA.ORCID 0000-0002-0545-2183
Saint Michael's College · US

Funding

Vermont INBRE Administrative Supplement 2024 AWD 118P20GM103449 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI CHRISTOPHER S FRANCKLYN · 2012 to 2026
$58.4M
NIGMS NIH HHS P20 GM103449
6 · The paper itself

Abstract

Neurodegenerative diseases are among the main causes of death in the United States, leading to irreversible disintegration of neurons. Despite intense international research efforts, cellular mechanisms that initiate neurodegeneration remain elusive, thus inhibiting the development of effective preventative and early onset medical treatment. To identify underlying cellular mechanisms that initiate neuron degeneration, it is critical to identify histological and cellular hallmarks that can be linked to underlying biochemical processes. Due to the poor tissue preservation of degenerating mammalian brain tissue, our knowledge regarding histopathological hallmarks of early to late degenerative stages is only fragmentary. Here, we introduce a novel model organism to study histological hallmarks of neurodegeneration, the spider Cupiennius salei. We utilized toluidine blue-stained 0.9-μm serial semithin and 50-nm ultrathin sections of young and old spider nervous tissue. Our findings suggest that the initial stages of neurodegeneration in spiders may be triggered by (1) dissociation of neuron- and glia-derived microtubules, and (2) the weakening of microtubule-associated desmosomal junctions that lead to the unraveling of neuron-insulating macroglia, compromising the structural integrity of affected neurons. The involvement of macroglia in the disposal of neuronal debris described here-although different in the proposed transport mechanisms-shows resemblance to the mammalian glymphatic system. We propose that this model system is highly suitable to investigate invertebrate neurodegenerative processes from early onset to scar formation and that this knowledge may be useful for the study of neurodegeneration in mammalian tissue.

Indexed as

NeuronsSpidersAnimalsBrainCell AdhesionInvertebratesMammalsMicrotubulescell adhesionCupiennius saleidesmosomesmacrogliamicrotubules

Identifiers

PMID36594894
PMCPMC10037207
OpenAlexW4313488491

What OpenQuestion holds

Textmetadata
LicenceTDM
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 OpenQuestion graph.