Evidence map›Paper›PMID 40595215›Full record

ArticleScientific reports2025

Extracellular vesicles derived from Lactobacillus gasseri GFC-1220 alleviate inflammation via the TLR4/NF-κB signaling pathway in LPS-stimulated RAW264.7 macrophages.

Jin-Ah Koh, Minh Ha Le, Hyo-Jun Lee, Jin-Woo Min, Mi Jung Kim, Hee-Cheol Kang, Yeon-Ju Kim

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
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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

7 authors.

Jin-Ah Koh *JOR R&D Co.Ltd, 99, Masan 1-Gil, Jinwi-myeon, Pyeongtaek-si, Gyeonggi-do, Republic of Korea.
Minh Ha Le *Graduate School of Biotechnology, and College of Life Science, Kyung Hee University, Yongin-si, 17104, Gyeonggi-do, Republic of Korea.
Hyo-Jun LeeGraduate School of Biotechnology, and College of Life Science, Kyung Hee University, Yongin-si, 17104, Gyeonggi-do, Republic of Korea.
Jin-Woo MinGFC Life Science Co.,Ltd, Hwaseong, 18471, Republic of Korea.
Mi Jung KimGFC Life Science Co.,Ltd, Hwaseong, 18471, Republic of Korea.
Hee-Cheol KangGFC Life Science Co.,Ltd, Hwaseong, 18471, Republic of Korea.
Yeon-Ju KimGraduate School of Biotechnology, and College of Life Science, Kyung Hee University, Yongin-si, 17104, Gyeonggi-do, Republic of Korea. yeonjukim@khu.ac.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studies on the impact of gram-positive extracellular vesicles have paved the way for novel medical advancements. These vesicles serve as efficient carriers of microbial molecules to target cells, thereby influencing human pathophysiological processes. Thus, this study aimed to investigate the anti-inflammatory properties of extracellular vesicles derived from Lactobacillus gasseri GFC-1220 (LEVs) in lipopolysaccharide (LPS)-stimulated RAW264.7 macrophages. LEVs were characterized using transmission electron microscopy, nanoparticle tracking analysis, and dynamic light scattering measurements to examine their morphology, size, and concentration. We further assessed the anti-inflammatory effects of LEVs and their underlying mechanism in LPS-stimulated RAW264.7 macrophages. Our findings revealed that LEVs did not cause cytotoxic effects and significantly decreased the level of mitochondria superoxide and reactive oxygen species production. In addition, these vesicles effectively inhibited the LPS-induced activation of TLR4/NF-κB signaling pathway, consequently suppressing the secretion and expression of various pro-inflammatory mediators and cytokines. These included a reduction in the production of NO and PGE

Indexed as

Extracellular VesiclesInflammationLactobacillus gasseriMacrophagesNF-kappa BSignal TransductionToll-Like Receptor 4AnimalsAnti-Inflammatory AgentsCytokinesLipopolysaccharidesMiceRAW 264.7 CellsReactive Oxygen SpeciesAnti-Inflammatory AgentsCytokinesLipopolysaccharidesNF-kappa BReactive Oxygen SpeciesTlr4 protein, mouseToll-Like Receptor 4Anti-inflammatory effectsExtracellular vesiclesLactobacillus gasseri GFC-1220Macrophages

Identifiers

PMID40595215
PMCPMC12215889

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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.