Evidence map›Paper›PMID 27400875›Full record

ArticleJournal of neuroinflammation2016

Transcriptome sequencing reveals that LPS-triggered transcriptional responses in established microglia BV2 cell lines are poorly representative of primary microglia.

Amitabh Das, Sun Hwa Kim, Sarder Arifuzzaman, Taeho Yoon, Jin Choul Chai, Young Seek Lee, Kyoung Sun Park, Kyoung Hwa Jung, Young Gyu Chai

Open access · goldAbstract read
In one paragraph

Article in Journal of neuroinflammation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed
5.1field-weighted citation impact, top 5% 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

94 citing papers in PubMed, 154 citations in OpenAlex.

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  14. Forced polarisation of microglia by IL-13 is modified by inflammatory and microenvironmental context.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
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34 more citing papers are in PubMed but not listed here.

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

9 authors at 1 institution in 1 country.

Amitabh DasInstitute of Natural Science and Technology, Hanyang University, Ansan, 15588, Republic of Korea.
Sun Hwa KimDepartment of Molecular and Life Sciences, Hanyang University, Ansan, 15588, Republic of Korea.
Sarder ArifuzzamanDepartment of Bionanotechnology, Hanyang University, Seoul, 04673, Republic of Korea.
Taeho YoonDepartment of Molecular and Life Sciences, Hanyang University, Ansan, 15588, Republic of Korea.
Jin Choul ChaiDepartment of Molecular and Life Sciences, Hanyang University, Ansan, 15588, Republic of Korea.
Young Seek LeeDepartment of Molecular and Life Sciences, Hanyang University, Ansan, 15588, Republic of Korea.
Kyoung Sun ParkInstitute of Natural Science and Technology, Hanyang University, Ansan, 15588, Republic of Korea.
Kyoung Hwa JungInstitute of Natural Science and Technology, Hanyang University, Ansan, 15588, Republic of Korea. khjung2@gmail.com.
Young Gyu ChaiDepartment of Molecular and Life Sciences, Hanyang University, Ansan, 15588, Republic of Korea. ygchai@hanyang.ac.kr.
Hanyang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicroglia are resident myeloid cells in the CNS that are activated by infection, neuronal injury, and inflammation. Established BV2 microglial cell lines have been the primary in vitro models used to study neuroinflammation for more than a decade because they reduce the requirement of continuously maintaining cell preparations and animal experimentation models. However, doubt has recently been raised regarding the value of BV2 cell lines as a model system.

methodsWe used triplicate RNA sequencing (RNA-seq) to investigate the molecular signature of primary and BV2 microglial cell lines using two transcriptomic techniques: global transcriptomic biological triplicate RNA-seq and quantitative real-time PCR. We analyzed differentially expressed genes (DEGs) to identify transcription factor (TF) motifs (-950 to +50 bp of the 5' upstream promoters) and epigenetic mechanisms.

resultsSequencing assessment and quality evaluation revealed that primary microglia have a distinct transcriptomic signature and express a unique cluster of transcripts in response to lipopolysaccharide. This microglial signature was not observed in BV2 microglial cell lines. Importantly, we observed that previously unidentified TFs (i.e., IRF2, IRF5, IRF8, STAT1, STAT2, and STAT5A) and the epigenetic regulators KDM1A, NSD3, and SETDB2 were significantly and selectively expressed in primary microglia (PM). Although transcriptomic alterations known to occur in BV2 microglial cell lines were identified in PM, we also observed several novel transcriptomic alterations in PM that are not frequently observed in BV2 microglial cell lines.

conclusionsCollectively, these unprecedented findings demonstrate that established BV2 microglial cell lines are probably a poor representation of PM, and we establish a resource for future studies of neuroinflammation.

Indexed as

Analysis of VarianceAnimalsAnimals, NewbornBrainCells, CulturedCytokinesDose-Response Relationship, DrugGene Expression RegulationLipopolysaccharidesMiceMicrogliaRNA, MessengerSignal TransductionTime FactorsToll-Like Receptor 4Transcription FactorsCytokinesLipopolysaccharidesRNA, MessengerTlr4 protein, mouseToll-Like Receptor 4Transcription FactorsGene regulationInnate immunityMicrogliaRNA sequencingTranscription factors

Identifiers

PMID27400875
PMCPMC4940985
OpenAlexW2462327766

What OpenQuestion holds

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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 OpenQuestion graph.