The function and mechanism of Human nasal mucosa-derived mesenchymal stem cells in allergic rhinitis in mice.

IF 4.8 3区 医学 Q2 CELL BIOLOGY Inflammation Research Pub Date : 2024-10-01 Epub Date: 2024-08-24 DOI:10.1007/s00011-024-01933-1
Yuan Liu, Shengyang Liu, Linghui Meng, Li Fang, Jinzhuang Yu, Jing Yue, Tao Li, Yanyi Tu, Tianjiao Jiang, Peng Yu, Yu-Zhu Wan, Yongtian Lu, Li Shi
{"title":"The function and mechanism of Human nasal mucosa-derived mesenchymal stem cells in allergic rhinitis in mice.","authors":"Yuan Liu, Shengyang Liu, Linghui Meng, Li Fang, Jinzhuang Yu, Jing Yue, Tao Li, Yanyi Tu, Tianjiao Jiang, Peng Yu, Yu-Zhu Wan, Yongtian Lu, Li Shi","doi":"10.1007/s00011-024-01933-1","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>To investigate the immunomodulatory effects and potential mechanisms of human nasal mucosa-derived mesenchymal stem cells(hNMSCs) on mouse allergic rhinitis, and to compare them with human umbilical cord-derived mesenchymal stem cells (hUCMSCs).</p><p><strong>Method: </strong>hNMSCs and hUCMSCs were isolated and cultured for identification from human nasal mucosa and umbilical cord tissues. A co-culture system of LPS-stimulated RAW264.7 cells/mouse peritoneal macrophages and MSCs was employed.Changes in inflammatory factors in RAW264.7 cells and the culture medium as well as the expression of NF-κB signaling pathway in RAW264.7 cells were detected. Forty-eight BALB/c mice were randomly divided into control, OVA, hNMSCs, and hUCMSCs groups. An allergic rhinitis (AR) model was established through ovalbumin (OVA) stimulation and treated with hNMSCs and hUCMSCs. Subsequent assessments included related symptoms, biological changes, and the expression of the NF-κB signaling pathway in the nasal mucosa of mice.</p><p><strong>Results: </strong>MSCs can be successfully isolated from human nasal mucosa. Both hNMSCs and hUCMSCs interventions significantly reverseed the inflammation induced by LPS and suppressed the upregulation of the NF-κB signaling pathway in RAW264.7 cells. Treatment with hNMSCs and hUCMSCs alleviated mouse allergic symptoms, reduced levels of total IgE, OVA-specific IgE and IgG1 in mouse serum, TH2-type cytokines and chemokines in mouse nasal mucosa, and TH2-type cytokines in mouse spleen culture medium, while also inhibiting the expression of the NF-κB signaling pathway in the nasal mucosa of mice. moreover, the hNMSCs group showed a more significant reduction in OVA-specific IgG1 in serum and IL-4 expression levels in mouse spleen culture medium compared to the hUCMSCs group.</p><p><strong>Conclusion: </strong>Our findings suggest that hNMSCs can ameliorate allergic rhinitis in mice, with a certain advantage in anti-inflammatory effects compared to hUCMSCs. The NF-κB pathway is likely involved in the anti-inflammatory regulation process by hNMSCs.Therefore, hNMSCs might represent a novel therapeutic approach for allergic rhinitis.</p>","PeriodicalId":13550,"journal":{"name":"Inflammation Research","volume":" ","pages":"1819-1832"},"PeriodicalIF":4.8000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11445352/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inflammation Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00011-024-01933-1","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/24 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose: To investigate the immunomodulatory effects and potential mechanisms of human nasal mucosa-derived mesenchymal stem cells(hNMSCs) on mouse allergic rhinitis, and to compare them with human umbilical cord-derived mesenchymal stem cells (hUCMSCs).

Method: hNMSCs and hUCMSCs were isolated and cultured for identification from human nasal mucosa and umbilical cord tissues. A co-culture system of LPS-stimulated RAW264.7 cells/mouse peritoneal macrophages and MSCs was employed.Changes in inflammatory factors in RAW264.7 cells and the culture medium as well as the expression of NF-κB signaling pathway in RAW264.7 cells were detected. Forty-eight BALB/c mice were randomly divided into control, OVA, hNMSCs, and hUCMSCs groups. An allergic rhinitis (AR) model was established through ovalbumin (OVA) stimulation and treated with hNMSCs and hUCMSCs. Subsequent assessments included related symptoms, biological changes, and the expression of the NF-κB signaling pathway in the nasal mucosa of mice.

Results: MSCs can be successfully isolated from human nasal mucosa. Both hNMSCs and hUCMSCs interventions significantly reverseed the inflammation induced by LPS and suppressed the upregulation of the NF-κB signaling pathway in RAW264.7 cells. Treatment with hNMSCs and hUCMSCs alleviated mouse allergic symptoms, reduced levels of total IgE, OVA-specific IgE and IgG1 in mouse serum, TH2-type cytokines and chemokines in mouse nasal mucosa, and TH2-type cytokines in mouse spleen culture medium, while also inhibiting the expression of the NF-κB signaling pathway in the nasal mucosa of mice. moreover, the hNMSCs group showed a more significant reduction in OVA-specific IgG1 in serum and IL-4 expression levels in mouse spleen culture medium compared to the hUCMSCs group.

Conclusion: Our findings suggest that hNMSCs can ameliorate allergic rhinitis in mice, with a certain advantage in anti-inflammatory effects compared to hUCMSCs. The NF-κB pathway is likely involved in the anti-inflammatory regulation process by hNMSCs.Therefore, hNMSCs might represent a novel therapeutic approach for allergic rhinitis.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
人鼻黏膜间充质干细胞在小鼠过敏性鼻炎中的功能和机制。
目的:研究人鼻黏膜间充质干细胞(hNMSCs)对小鼠过敏性鼻炎的免疫调节作用及其潜在机制,并将其与人脐带间充质干细胞(hUCMSCs)进行比较。方法:从人鼻黏膜和脐带组织中分离并培养鉴定hNMSCs和hUCMSCs。采用 LPS 刺激的 RAW264.7 细胞/小鼠腹腔巨噬细胞和间充质干细胞共培养系统,检测 RAW264.7 细胞和培养液中炎性因子的变化以及 RAW264.7 细胞中 NF-κB 信号通路的表达。48 只 BALB/c 小鼠被随机分为对照组、OVA 组、hNMSCs 组和 hUCMSCs 组。通过卵清蛋白(OVA)刺激建立过敏性鼻炎(AR)模型,并用 hNMSCs 和 hUCMSCs 治疗。随后的评估包括相关症状、生物学变化以及小鼠鼻粘膜中 NF-κB 信号通路的表达:结果:间充质干细胞可成功从人类鼻粘膜中分离出来。hNMSCs和hUCMSCs干预均能显著逆转LPS诱导的炎症,并抑制NF-κB信号通路在RAW264.7细胞中的上调。用 hNMSCs 和 hUCMSCs 治疗可减轻小鼠的过敏症状,降低小鼠血清中总 IgE、OVA 特异性 IgE 和 IgG1 的水平,降低小鼠鼻粘膜中 TH2 型细胞因子和趋化因子的水平,以及小鼠脾脏培养液中 TH2 型细胞因子的水平,同时还能抑制小鼠鼻粘膜中 NF-κB 信号通路的表达。此外,与 hUCMSCs 组相比,hNMSCs 组小鼠血清中 OVA 特异性 IgG1 和脾培养液中 IL-4 表达水平的降低更为显著:我们的研究结果表明,hNMSCs 可改善小鼠过敏性鼻炎,与 hUCMSCs 相比,其抗炎作用具有一定优势。NF-κB通路可能参与了hNMSCs的抗炎调节过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Inflammation Research
Inflammation Research 医学-免疫学
CiteScore
9.90
自引率
1.50%
发文量
134
审稿时长
3-8 weeks
期刊介绍: Inflammation Research (IR) publishes peer-reviewed papers on all aspects of inflammation and related fields including histopathology, immunological mechanisms, gene expression, mediators, experimental models, clinical investigations and the effect of drugs. Related fields are broadly defined and include for instance, allergy and asthma, shock, pain, joint damage, skin disease as well as clinical trials of relevant drugs.
期刊最新文献
Gastrin-releasing peptide receptor antagonist RC-3095 inhibits Porphyromonas gingivalis lipopolysaccharide-accelerated atherosclerosis by suppressing inflammatory responses in endothelial cells and macrophages. Inhibition of glycolytic reprogramming suppresses innate immune-mediated inflammation in experimental amyotrophic lateral sclerosis. Calprotectin is regulated by IL-17A and induces steroid hyporesponsiveness in asthma. Treatment with lipoxin A4 improves influenza A infection outcome, induces macrophage reprogramming, anti-inflammatory and pro-resolutive responses. A novel molecular classification based on efferocytosis-related genes for predicting clinical outcome and treatment response in acute myeloid leukemia.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1