Evidence map›Paper›PMID 32315669›Full record

ArticleJournal of neuroscience methods2020

Isolation, culture, and downstream characterization of primary microglia and astrocytes from adult rodent brain and spinal cord.

Nilesh M Agalave, Brandon T Lane, Prapti H Mody, Thomas A Szabo-Pardi, Michael D Burton

Open access · greenAbstract read
In one paragraph

Article in Journal of neuroscience methods, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 59 citations in OpenAlex.

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  11. Isolation of Primary Brain Cells: Challenges and Solutions.Archives of clinical and biomedical research · 2025
    Article
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  14. Mouse serum albumin induces neuronal apoptosis and tauopathies.Acta neuropathologica communications · 2024
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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

5 authors at 1 institution in 1 country.

Nilesh M AgalaveNeuroimmunology and Behavior Laboratory, School of Behavioral and Brain Sciences, Center for Advanced Pain Studies, University of Texas at Dallas, Richardson, Texas, USA.
Brandon T LaneNeuroimmunology and Behavior Laboratory, School of Behavioral and Brain Sciences, Center for Advanced Pain Studies, University of Texas at Dallas, Richardson, Texas, USA.
Prapti H ModyNeuroimmunology and Behavior Laboratory, School of Behavioral and Brain Sciences, Center for Advanced Pain Studies, University of Texas at Dallas, Richardson, Texas, USA.
Thomas A Szabo-PardiNeuroimmunology and Behavior Laboratory, School of Behavioral and Brain Sciences, Center for Advanced Pain Studies, University of Texas at Dallas, Richardson, Texas, USA.
Michael D BurtonNeuroimmunology and Behavior Laboratory, School of Behavioral and Brain Sciences, Center for Advanced Pain Studies, University of Texas at Dallas, Richardson, Texas, USA. Electronic address: Michael.Burton@utdallas.edu.
The University of Texas at Dallas · US

Funding

Mechanisms involved in postoperative recovery: a focus on pain, delirium, and neuroinflammationR35GM147094 · NIGMS · UNIVERSITY OF TEXAS DALLAS · PI Michael D Burton · 2022 to 2026
$1.9M
The Role of Cell-specific TLR-4 Signaling in Developing Chronic PainK22NS096030 · NINDS · UNIVERSITY OF TEXAS DALLAS · PI BURTON, MICHAEL D · 2016 to 2019
$838k
NIGMS NIH HHS R35 GM147094NINDS NIH HHS K22 NS096030
6 · The paper itself

Abstract

backgroundNeuroimmunologists aspire to understand the interactions between neurons, microglia, and astrocytes in the CNS. To study these cells, researchers work with either immortalized cell lines or primary cells acquired from animal tissue. Primary cells reflect in vivo characteristics and functionality compared to immortalized cells; however, they are challenging to acquire and maintain. NEW

methodEstablished protocols to harvest primary glia use neonatal rodents, here we provide a method for simultaneously isolating microglia and astrocytes from brain and/or spinal cord from adult rodents. We utilized a discontinuous percoll density gradient enabling easy discrimination of these cell populations without enzymatic digestion or complex sorting techniques.

resultsWe found cells isolated from the percoll interface between 70 %-50 % were microglia, as they express ionizing calcium-binding adaptor molecule 1 (Iba1) in immunocytochemistry and CD11b COMPARISON WITH EXISTING

methodsOur method allows for rapid isolation of both microglia and astrocytes in one protocol with relatively few resources, preserves cellular phenotype, and yields high cell numbers without magnetic or antibody sorting.

conclusionHere we show a novel, single protocol to isolate microglia and astrocytes from brain and spinal cord tissue, allowing for culturing and other downstream applications from the cells of animals of various ages, which will be useful for researchers investigating these two major glial cell types from the brain or spinal cord of the same rodent.

Indexed as

AstrocytesMicrogliaAnimalsBrainGlial Fibrillary Acidic ProteinRodentiaSpinal CordGlial Fibrillary Acidic ProteinAstrocytesCultureELISAFlow cytometryIL-6ImmunocytochemistryIsolationMicroglia

Identifiers

PMID32315669
PMCPMC7293863
OpenAlexW3016318794

What OpenQuestion holds

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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.