Evidence map›Paper›PMID 38256090›Full record

ArticleInternational journal of molecular sciences2024

Porcine β-Defensin 114: Creating a Dichotomous Response to Inflammation.

Guoqi Su, Sheng Huang, Shan Jiang, Li Chen, Feiyun Yang, Zuohua Liu, Guixue Wang, Jinxiu Huang

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Porcine β-Defensin 2 Expressed inAnimals : an open access journal from MDPI · 2025
    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

8 authors at 2 institutions in 1 country.

Guoqi SuChongqing Academy of Animal Sciences, Chongqing 402460, China.
Sheng HuangChongqing Academy of Animal Sciences, Chongqing 402460, China.
Shan JiangChongqing Academy of Animal Sciences, Chongqing 402460, China.
Li ChenChongqing Academy of Animal Sciences, Chongqing 402460, China.
Feiyun YangChongqing Academy of Animal Sciences, Chongqing 402460, China.
Zuohua LiuChongqing Academy of Animal Sciences, Chongqing 402460, China.
Guixue WangKey Laboratory of Biorheological Science & Technology, Ministry of Education, State & Local Joint Engineering Laboratory for Vascular Implants, College of Bioengineering, Chongqing University, Chongqing 402460, China.ORCID 0000-0002-9192-8757
Jinxiu HuangChongqing Academy of Animal Sciences, Chongqing 402460, China.
Chongqing Academy of Animal Science · CNChongqing University · CN

Funding

National Key Research and Development Plan 2022YFC2105003Research Institutions Performance Guidance Project cstc2021jxjl80001
6 · The paper itself

Abstract

The immunity-related functions of defensins seem to be dependent on environmental stimuli, the cell type, and the concentration of peptides. However, the function and mechanism of porcine β-defensin 114 (pBD114) in regulating the inflammatory response to macrophages are unclear. Therefore, the modulatory effects of porcine pBD114 on the inflammatory response were investigated by treating the mouse monocyte macrophage cell line RAW264.7 with different concentrations of pBD114 with or without lipopolysaccharide (LPS). RNA-seq analysis was performed to investigate the mechanisms underlying pBD114's regulation of inflammatory responses in macrophages. In addition, the inflammatory response-modulating effects of pBD114 were also further verified with a mouse assay. The results showed that 100 μg/mL of pBD114 significantly promoted the secretion of TNF-α and IL-10 in RAW264.7. However, the LPS-induced increase in TNFα in the RAW264.7 cell cultures was significantly decreased with 10 μg/mL of pBD114. These results suggest that pBD114 can exhibit pro-inflammatory activities under normal physiological conditions with 100 μg/mL of pBD114, and anti-inflammatory activities during an excessive inflammatory response with 10 μg/mL of pBD114. RNA-seq analysis was performed to gain further insights into the effects of pBD114 on the inflammatory response. Among the pBD114-promoting RAW264.7 pro-inflammatory responses, pBD114 significantly up-regulated 1170 genes and down-regulated 724 genes. KEGG enrichment showed that the differentially expressed genes (DEGs) were significantly enriched in the immune- and signal-transduction-related signaling pathways. Protein-Protein Interaction (PPI) and key driver analysis (KDA) analyses revealed that

Indexed as

beta-DefensinsAnimalsAnti-Inflammatory AgentsInflammationLipopolysaccharidesMiceSignal TransductionSwineAnti-Inflammatory Agentsbeta-DefensinsLipopolysaccharidesinflammatory responselipopolysaccharidemiceRAW264.7RNA-seq

Identifiers

PMID38256090
PMCPMC10816359
OpenAlexW4390882111

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.