Evidence map›Paper›PMID 29105376›Full record

ArticleImmunity, inflammation and disease2018

Transcriptional and translational-uncoupling in regulation of the CXCL12 and its receptors CXCR4, 7 in THP-1 monocytes and macrophages.

Lu Yu, Liangli Yu, Quynhchi Pham, Thomas T Y Wang

Open access · goldAbstract read
In one paragraph

Article in Immunity, inflammation and disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-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

4 citing papers in PubMed, 10 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

Lu YuDepartment of Nutrition and Food Science, University of Maryland, College Park, Maryland, 20742, USA.ORCID 0000-0001-7901-8390
Liangli YuDepartment of Nutrition and Food Science, University of Maryland, College Park, Maryland, 20742, USA.
Quynhchi PhamUSDA, Diet, Genomics and Immunology Laboratory, Beltsville Human Nutrition Research Center, ARS, Beltsville, Maryland, 20705, USA.
Thomas T Y WangUSDA, Diet, Genomics and Immunology Laboratory, Beltsville Human Nutrition Research Center, ARS, Beltsville, Maryland, 20705, USA.
Beltsville Human Nutrition Research Center · USCenter for Food Safety and Applied Nutrition · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe chemokine CXCL12 and its receptors CXCR4 and 7 play crucial roles in the immune system. In the present study, regulation of this pathway was further examined using the in-vitro model of undifferentiated human THP-1 monocytes (u-THP-1) and phorbol 12-myristate 13-acetate (PMA)-differentiated THP-1 macrophages (d-THP-1), to assess the effects of differentiation and the TLR4 ligand lipopolysaccharide (LPS) on the pathway. METHODS/

resultsDifferentiation did not affect the CXCR4, 7 mRNA levels. Interestingly, the CXCL12 and CXCR7 proteins but not CXCR4 were found to be up-regulated during differentiation. LPS, through CD14-dependent pathway, induced CXCL12 and CXCR4, 7 mRNA levels to a greater magnitude in d- than u-THP-1. The induction effect on CXCL12 stimulated by LPS was confirmed using ELISA. Increased migration of u-THP-1 was observed using conditioned medium from LPS-treated d-THP-1. Additionally, d-THP-1, although expressed higher CXCR7 protein levels, failed to migrate toward CXCL12. In contrast, LPS did not affect CXCR4, 7 protein levels.

conclusionHence, this study indicated that CXCL12, CXCR4, and CXCR7 were differentially expressed and regulated in u-THP-1 and d-THP-1 cells in response to external stimuli. Importantly, we reported here a novel observation that uncoupling exists between transcriptional and translational regulation of CXCR4, 7 expressions by differentiation and TLR stimuli.

Indexed as

Chemokine CXCL12HumansLipopolysaccharidesMacrophagesMonocytesProtein BiosynthesisReceptors, CXCRReceptors, CXCR4THP-1 CellsTranscription, GeneticACKR3 protein, humanChemokine CXCL12CXCL12 protein, humanCXCR4 protein, humanLipopolysaccharidesReceptors, CXCRReceptors, CXCR4CXCL12CXCR4CXCR7LipopolysaccharideTHP-1

Identifiers

PMID29105376
PMCPMC5818454
OpenAlexW2765412817

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Registered trials

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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.