Evidence map›Paper›PMID 37488799›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2023

[LRG1 inhibits hepatic macrophage activation by enhancing TGF-β1 signaling to alleviate MAFLD in mice].

L Xu, J Han, Z Yang, Y Yang, J Chen, X Wu, Q Wang, Y Hong

Open access · greenAbstract readEnglish Abstract
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. High glucose induces pro-inflammatory polarization of macrophages by inhibiting immune-responsive gene 1 expression.Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2025
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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.

L XuDepartment of Histology and Embryology, School of Basic Medical Sciences, Guizhou Medical University, Guiyang 550025, China.
J HanDepartment of Histology and Embryology, School of Basic Medical Sciences, Guizhou Medical University, Guiyang 550025, China.
Z YangDepartment of Histology and Embryology, School of Basic Medical Sciences, Guizhou Medical University, Guiyang 550025, China.
Y YangDepartment of Histology and Embryology, School of Basic Medical Sciences, Guizhou Medical University, Guiyang 550025, China.
J ChenDepartment of Histology and Embryology, School of Basic Medical Sciences, Guizhou Medical University, Guiyang 550025, China.
X WuClinical Laboratory, Jinyang Hospital, Guizhou Medical University, Guiyang 550025, China.
Q WangDepartment of Histology and Embryology, School of Basic Medical Sciences, Guizhou Medical University, Guiyang 550025, China.
Y HongDepartment of Histology and Embryology, School of Basic Medical Sciences, Guizhou Medical University, Guiyang 550025, China.
Guiyang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo explore the effect of leucine-rich α-2-glycoprotein (LRG1) derived from hepatocytes on activation of hepatic M1 Kupffer cells.

methodsA metabolic dysfunction-associated fatty liver disease (MAFLD) model was established in BALB/c mice by high-fat diet (HFD) feeding for 16 weeks. Oleic acid was used to induce steatosis in primary cultures of mouse hepatocytes. The mRNA and protein expressions of LRG1 in mouse liver tissues and hepatocytes were detected by real-time PCR and Western blotting. Primary hepatic macrophages were stimulated with the conditioned medium (CM) from steatotic hepatocyte along with LRG1 or transforming growth factor-β1 (TGF-β1), or both for 24 h, and the expression levels of inducible nitric oxide synthase (iNOS) was detected with Western botting, and the mRNA expressions of iNOS, chemokine ligand 1 (CXCL-1) and interleukin-1β (IL-1β) were measured by RT-PCR. The MAFLD mice were injected with LRG1 (

resultsThe mRNA and protein expression levels of LRG1 were significantly downregulated in the liver tissues of MAFLD mice and steatotic hepatocytes (

conclusionLRG1 inhibits hepatic macrophage infiltration by enhancing TGF-β1 signaling to alleviate fatty liver inflammation in MAFLD mice.

Indexed as

Non-alcoholic Fatty Liver DiseaseTransforming Growth Factor beta1AnimalsCulture Media, ConditionedGlycoproteinsMacrophage ActivationMiceSignal TransductionCulture Media, ConditionedGlycoproteinsLRG1 protein, mouseTransforming Growth Factor beta1hepatic macrophagesleucine-rich α-2-glycoprotein 1metabolic dysfunction-associated fatty liver diseasesteatosistransforming growth factor-β1

Identifiers

PMID37488799
PMCPMC10366524
OpenAlexW4385230710

What OpenQuestion holds

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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.