Evidence map›Paper›PMID 29403501›Full record

ArticleFrontiers in immunology2018

High-Resolution Mapping and Dynamics of the Transcriptome, Transcription Factors, and Transcription Co-Factor Networks in Classically and Alternatively Activated Macrophages.

Amitabh Das, Chul-Su Yang, Sarder Arifuzzaman, Sojin Kim, Sun Young Kim, Kyoung Hwa Jung, Young Seek Lee, Young Gyu Chai

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

51 citing papers in PubMed, 1 synthesis or guideline pooled it, 73 citations in OpenAlex.

  1. Lipopolysaccharide-mediated macrophage polarization, conserved pathogenesis, and implications for peripheral neuropathy: a systematic review.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Pooled it
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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

8 authors at 1 institution in 1 country.

Amitabh DasInstitute of Natural Science and Technology, Hanyang University, Ansan, South Korea.
Chul-Su YangDepartment of Molecular and Life Sciences, Hanyang University, Ansan, South Korea.
Sarder ArifuzzamanDepartment of Bionanotechnology, Hanyang University, Seoul, South Korea.
Sojin KimDepartment of Molecular and Life Sciences, Hanyang University, Ansan, South Korea.
Sun Young KimDepartment of Molecular and Life Sciences, Hanyang University, Ansan, South Korea.
Kyoung Hwa JungInstitute of Natural Science and Technology, Hanyang University, Ansan, South Korea.
Young Seek LeeDepartment of Molecular and Life Sciences, Hanyang University, Ansan, South Korea.
Young Gyu ChaiDepartment of Molecular and Life Sciences, Hanyang University, Ansan, South Korea.
Hanyang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophages are the prime innate immune cells of the inflammatory response, and the combination of multiple signaling inputs derived from the recognition of host factors [e.g., interferon-g (IFN-γ)] and invading pathogen products (e.g., toll-like receptors (TLRs) agonists) are required to maintain essential macrophage function. The profound effects on biological outcomes of inflammation associated with IFN-γ pretreatment ("priming") and TLR4 ligand bacterial lipopolysaccharide (LPS)-induced macrophage activation (M1 or classical activation) have long been recognized, but the underlying mechanisms are not well defined. Therefore, we analyzed gene expression profiles of macrophages and identified genes, transcription factors (TFs), and transcription co-factors (TcoFs) that are uniquely or highly expressed in IFN-γ-mediated TLR4 ligand LPS-inducible versus only TLR4 ligand LPS-inducible primary macrophages. This macrophage gene expression has not been observed in macrophage cell lines. We also showed that interleukin (IL)-4 and IL-13 (M2 or alternative activation) elicited the induction of a distinct subset of genes related to M2 macrophage polarization. Importantly, this macrophage gene expression was also associated with promoter conservation. In particular, our approach revealed novel roles for the TFs and TcoFs in response to inflammation. We believe that the systematic approach presented herein is an important framework to better understand the transcriptional machinery of different macrophage subtypes.

Indexed as

AnimalsBone Marrow CellsCell LineGene Expression ProfilingInterferon-gammaInterleukin-13LipopolysaccharidesMacrophage ActivationMacrophagesMiceMice, Inbred C57BLRAW 264.7 CellsToll-Like Receptor 4Transcription FactorsIFNG protein, mouseInterferon-gammaInterleukin-13LipopolysaccharidesTlr4 protein, mouseToll-Like Receptor 4Transcription Factorsinterferon-glipopolysaccharidemacrophagesRNA-sequencingtranscription factors

Identifiers

PMID29403501
PMCPMC5778122
OpenAlexW2786007302

What OpenQuestion holds

Textmetadata
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.