Evidence map›Paper›PMID 40467844›Full record

ArticleCommunications biology2025

BHLHE40 contributes to allergic asthma progression in mice through NRTN downregulation in macrophages.

Bing Dai, Li Chen, Xiaowen Li, Qianlan Zhou, Qinzhen Zhang, Lina Han, Wenxin Shen, Qing Chang, Yuhong Zhao, Si Liu and 1 more

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Bing Dai *Department of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, China.
Li Chen *Department of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, China.
Xiaowen Li *Department of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, China.
Qianlan ZhouDepartment of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, China.
Qinzhen ZhangDepartment of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, China.
Lina HanDepartment of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, China.
Wenxin ShenDepartment of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, China.
Qing ChangLiaoning Key Laboratory of Precision Medical Research on Major Chronic Disease, Clinical Research Center of Shengjing Hospital of China Medical University, Shenyang, China.
Yuhong ZhaoDepartment of Clinical Epidemiology, Shengjing Hospital of China Medical University, Shenyang, China. zhaoyuhong@sj-hospital.org.ORCID http://orcid.org/0000-0003-4265-6692
Si LiuDepartment of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, China. liusi@sj-hospital.org.ORCID http://orcid.org/0009-0003-2812-3328
Lishen ShanDepartment of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, China. shanls@sj-hospital.org.ORCID http://orcid.org/0009-0005-8491-2449

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alternatively activated M2-like macrophages have a profound impact on asthma pathogenesis. Basic Helix-Loop-Helix Family Member E40 (BHLHE40), a dimeric transcriptional factor, plays a key regulation in macrophage functions. Here we show that ovalbumin (OVA)-challenged mice exhibited greater expression of BHLHE40 in lung tissues. Bhlhe40 knockdown reduced the pulmonary lesions and allergy-induced inflammation in asthmatic mice. Moreover, an inhibitory effect of Bhlhe40 knockdown on alternative activation was observed in vivo and in vitro. We show a downstream target Neurturin (Nrtn) of Bhlhe40. Dual luciferase assay and ChIP-qPCR assay indicated that BHLHE40 bound to Nrtn promoter and reduced its transcriptional activity. Simultaneous knockdown of Bhlhe40 and Nrtn recovered the alternative activation of macrophages and rescued the OVA-elicited asthma phenotype. NRTN downregulation offset the alleviative effects of Bhlhe40 knockdown on asthma. This study demonstrates that BHLHE40 promotes allergic asthma, and contributes to the alternative activation of macrophages in asthma by inhibiting Nrtn transcription.

Indexed as

AsthmaBasic Helix-Loop-Helix ProteinsMacrophagesAnimalsDisease Models, AnimalDisease ProgressionDown-RegulationFemaleGene Knockdown TechniquesHomeodomain ProteinsMiceMice, Inbred BALB COvalbuminBasic Helix-Loop-Helix ProteinsBhlhe40 protein, mouseHomeodomain ProteinsOvalbumin

Identifiers

PMID40467844
PMCPMC12137885

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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.