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

被引:0
|
作者
Liu, Yuan [1 ,2 ]
Liu, Shengyang [1 ,3 ,5 ]
Meng, Linghui [1 ,3 ]
Fang, Li [2 ]
Yu, Jinzhuang [1 ,3 ,5 ]
Yue, Jing [4 ]
Li, Tao [1 ,3 ,5 ]
Tu, Yanyi [1 ,3 ,5 ]
Jiang, Tianjiao [1 ,3 ,5 ]
Yu, Peng [1 ,3 ,5 ]
Wan, Yu-Zhu [1 ,3 ,5 ]
Lu, Yongtian [2 ]
Shi, Li [1 ,3 ,5 ]
机构
[1] Shandong Univ, Shandong Prov ENT Hosp, Dept Otolaryngol Head & Neck Surg, Duanxing West Rd, Jinan 250033, Shandong, Peoples R China
[2] Shenzhen Univ, Shenzhen Peoples Hosp 2, Affiliated Hosp 1, Dept Otorhinolaryngol, 3002 Sungang West Rd, Shenzhen 518000, Guangdong, Peoples R China
[3] Shandong Second Prov Gen Hosp, Dept Otolaryngol Head & Neck Surg, Jinan, Shandong, Peoples R China
[4] Shandong Second Prov Gen Hosp, Dept Tradit Chinese Med, Jinan, Shandong, Peoples R China
[5] Shandong Prov Key Med & Hlth Lab Airway Inflammato, Jinan, Peoples R China
基金
中国国家自然科学基金;
关键词
Allergic rhinitis; Mesenchymal stem cells; Anti-inflammation; NF-kappa B pathway; KAPPA-B; MOUSE MODEL; T-CELLS; INFLAMMATION; EXPRESSION; INTERLEUKIN-4; ACTIVATION; INDUCTION; PATHWAY; ASTHMA;
D O I
10.1007/s00011-024-01933-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
PurposeTo 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).MethodhNMSCs 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-kappa B 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-kappa B signaling pathway in the nasal mucosa of mice.ResultsMSCs 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-kappa B 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-kappa B 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.ConclusionOur findings suggest that hNMSCs can ameliorate allergic rhinitis in mice, with a certain advantage in anti-inflammatory effects compared to hUCMSCs. The NF-kappa B pathway is likely involved in the anti-inflammatory regulation process by hNMSCs.Therefore, hNMSCs might represent a novel therapeutic approach for allergic rhinitis.
引用
收藏
页码:1819 / 1832
页数:14
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