Evidence map›Paper›PMID 31152449›Full record

ArticleThe Journal of comparative neurology2019

DiI-mediated analysis of presynaptic and postsynaptic structures in human postmortem brain tissue.

Sujan C Das, Danli Chen, William Brandon Callor, Eric Christensen, Hilary Coon, Megan E Williams

Open access · greenAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 32% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
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  5. Review
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  7. Article
  8. Neural functions of small heat shock proteins.Neural regeneration research · 2022
    Review
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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

6 authors at 2 institutions in 1 country.

Sujan C DasDepartment of Psychiatry, University of Utah School of Medicine, Salt Lake City, Utah.
Danli ChenDepartment of Psychiatry, University of Utah School of Medicine, Salt Lake City, Utah.
William Brandon CallorUtah State Office of Medical Examiner, Utah Department of Health, Salt Lake City, Utah.
Eric ChristensenUtah State Office of Medical Examiner, Utah Department of Health, Salt Lake City, Utah.
Hilary CoonDepartment of Psychiatry, University of Utah School of Medicine, Salt Lake City, Utah.
Megan E WilliamsDepartment of Neurobiology and Anatomy, University of Utah School of Medicine, Salt Lake City, Utah.ORCID 0000-0002-5461-4126
University of Utah · USUtah Department of Health · US

Funding

Genetic analysis of high-risk Utah suicide pedigreesR01MH099134 · NIMH · UNIVERSITY OF UTAH · PI COON, HILARY · 2013 to 2017
$3.9M
The intellectual disability-associated gene kirrel3 in synapse developmentR01MH105426 · NIMH · UNIVERSITY OF UTAH · PI WILLIAMS, MEGAN ELISE · 2014 to 2018
$1.9M
NIMH NIH HHS R01 MH099134NIMH NIH HHS R01 MH105426
6 · The paper itself

Abstract

Most cognitive and psychiatric disorders are thought to be disorders of the synapse, yet the precise synapse defects remain unknown. Because synapses are highly specialized anatomical structures, defects in synapse formation and function can often be observed as changes in microscale neuroanatomy. Unfortunately, few methods are available for accurate analysis of synaptic structures in human postmortem tissues. Here, we present a methodological pipeline for assessing presynaptic and postsynaptic structures in human postmortem tissue that is accurate, rapid, and relatively inexpensive. Our method uses small tissue blocks from postmortem human brains, immersion fixation, lipophilic dye (DiI) labeling, and confocal microscopy. As proof of principle, we analyzed presynaptic and postsynaptic structures from hippocampi of 13 individuals aged 4 months to 71 years. Our results indicate that postsynaptic CA1 dendritic spine shape and density do not change in adults, while presynaptic DG mossy fiber boutons undergo significant structural rearrangements with normal aging. This suggests that mossy fiber synapses, which play a major role in learning and memory, may remain dynamic throughout life. Importantly, we find that human CA1 spine densities observed using this method on tissue that is up to 28 h postmortem is comparable to prior studies using tissue with much shorter postmortem intervals. Thus, the ease of our protocol and suitability on tissue with longer postmortem intervals should facilitate higher-powered studies of human presynaptic and postsynaptic structures in healthy and diseased states.

Indexed as

AdultAgedAutopsyChild, PreschoolFemaleHippocampusHumansInfantMaleMiddle AgedPresynaptic TerminalsStaining and LabelingSynapsesYoung Adultdendritic spineDiIhippocampusmossy fiber boutonpostmortem

Identifiers

PMID31152449
PMCPMC6790174
OpenAlexW2947727369

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.