Evidence map›Paper›PMID 32757372›Full record

ArticleNeuropsychopharmacology reports2020

A live imaging-friendly slice culture method using collagen membranes.

Ari Ogaki, Tasuku Araki, Masaya Ishikawa, Yuji Ikegaya, Ryuta Koyama

Open access · goldAbstract read
In one paragraph

Article in Neuropsychopharmacology reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

5 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Assessing Microglial Dynamics by Live Imaging.Frontiers in immunology · 2021
    Review
  5. 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 2 institutions in 1 country.

Ari OgakiLaboratory of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
Tasuku ArakiLaboratory of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
Masaya IshikawaIsehara Research Laboratory, Technology and Development Division, Kanto Chemical Co., Inc, Suzukawa, Isehara, Kanagawa, Japan.
Yuji IkegayaLaboratory of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
Ryuta KoyamaLaboratory of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.ORCID 0000-0001-7108-174X
The University of Tokyo · JPKanto Chemical (Japan) · JP

Funding

MOLECULAR GENETICS OF LIPOPROTEIN LIPASEF05TW003988 · FIC · UNIVERSITY OF WASHINGTON · PI AUWERX, JOHAN H · 1987 to 1988
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6 · The paper itself

Abstract

aimOrganotypic brain slice culture preserves the geographical position of neurons and neuronal circuits. The slice cultures also maintain both non-neuronal cell types and the surrounding extracellular matrix. The interface method has been widely used for slice cultures, in which brain slices are placed on semiporous polytetrafluoroethylene (PTFE) membranes. However, a low optical transparency of PTFE membrane makes it difficult to perform live imaging of deep regions of slice cultures using an inverted microscope. To overcome the issue, we evaluated the suitability of using collagen membranes for slice cultures, especially focusing on live imaging of the cellular dynamics of green fluorescent protein (GFP)-expressing microglia.

methodsEntorhinohippocampal slices were cultured on either collagen or PTFE membranes. The influence of membrane type on the ability to observe deep regions of slice cultures was examined by live imaging using an inverted microscope.

resultsCollagen membranes were thinner and had better optical transparency compared with PTFE membranes. There were no differences in cell viability, density of neurons or microglia. The densify of visible short branches of microglia in live imaging was higher in collagen membranes than PTFE membranes.

conclusionCollagen membranes are suitable for live imaging of cellular dynamics in slice cultures using an inverted microscope.

Indexed as

Membranes, ArtificialAnimalsAnimals, NewbornCollagenHippocampusMiceMice, Inbred C57BLMice, TransgenicOrgan Culture TechniquesCollagenMembranes, Artificialhippocampusimagingmicrogliaslice culturetime-lapse imaging

Identifiers

PMID32757372
PMCPMC7722644
OpenAlexW3047437840

What OpenQuestion holds

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LicenceCC BY
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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.