Evidence map›Paper›PMID 39023421›Full record

ArticleImmunity, inflammation and disease2024

Rat nasal mucosa-derived ectodermal mesenchymal stem cells: A new therapeutic option for chronic rhinosinusitis.

Liujin Li, ZhaoHui Liu, ChunLin Zhang, YiLin Long, TianWen Yang

Abstract read
In one paragraph

Article in Immunity, inflammation and disease, 2024. 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

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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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

5 authors.

Liujin LiAffiliated Hospital of Zunyi Medical University, Zunyi, China.ORCID 0009-0008-7363-2785
ZhaoHui LiuAffiliated Hospital of Zunyi Medical University, Zunyi, China.
ChunLin ZhangAffiliated Hospital of Zunyi Medical University, Zunyi, China.
YiLin LongAffiliated Hospital of Zunyi Medical University, Zunyi, China.
TianWen YangAffiliated Hospital of Zunyi Medical University, Zunyi, China.

Funding

Guizhou Provincial Health Care Commission on Provincial Medical Key Disciplines in 2023-2024 xm040191Zunyi Science and Technology Programme Zun Shi Ke He HZ Zi (2021) No. 75
6 · The paper itself

Abstract

objectiveTo investigate the effect of nasal mucosa-derived ectodermal mesenchymal stem cells (NM-EMSCs) on the inflammatory state of rats with chronic rhinosinusitis (CRS) and the underlying therapeutic mechanism.

methodsNM-EMSCs were isolated and extracted to construct a rat model of CRS. Fifteen Sprague‒Dawley (SD) rats were randomly divided into three groups: CK + NS group rats were injected locally with saline in the nasal mucosa; CRS + NS group rats were injected locally with saline in the nasal mucosa; and CRS + EMSCs group rats were injected locally with NM-EMSCs in the nasal mucosa. One rat from the CRS + EMSCs group was randomly euthanized at 2, 4, and 6 days after injection, and the nasal mucosa tissues were collected for HE staining, Masson's trichrome staining, and periodic acid-Schiff staining.

resultsNM-EMSCs specifically expressing CD73, CD105, and CD90 were successfully isolated from the nasal mucosa of rats and were able to differentiate into adipocytes, osteoblasts, and chondrocytes. After saline and NM-EMSC injection, compared with those in the blank control CK + NS group, the nasal mucosa in the CRS + NS and CRS + EMSC groups exhibited obvious thickening, a large amount of inflammatory cell infiltration, and increased collagen and mucin distribution. Four days post-NM-EMSC injection, the thickening of the nasal mucosa in the CRS group was gradually alleviated, the inflammatory cell infiltration gradually decreased, and the distribution of collagen and mucin and the collagen-positive area gradually decreased. Moreover, only a small number of inflammatory cells were visible, and the distribution of mucins was limited to 6 days post-NM-EMSC injection.

conclusionNM-EMSCs effectively attenuated inflammation in the nasal mucosa of CRS model rats.

Indexed as

Cell DifferentiationMesenchymal Stem CellsMesenchymal Stem Cell TransplantationNasal MucosaRats, Sprague-DawleyRhinitisSinusitisAnimalsCells, CulturedChronic DiseaseDisease Models, AnimalMaleRatsRhinosinusitiscell‐based therapychronic rhinosinusitisNM‐EMSCs

Identifiers

PMID39023421
PMCPMC11256880

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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.