[基于Notch1通路FTO调控养和平喘颗粒对哮喘BMSCs归巢的影响观察]。

细胞与分子免疫学杂志 Pub Date : 2025-07-01
Kun Wang, Haoxiang Fang, Xiaomei Cao
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引用次数: 0

摘要

目的观察Notch1通路m6A甲基化调控对哮喘患者骨髓间充质干细胞归巢的影响及中药复方养和平喘颗粒的干预研究。方法将大鼠骨间充质干细胞(BMSC)与支气管上皮细胞共培养。提取的细胞分为支气管上皮细胞组、哮喘支气管上皮细胞+间充质干细胞共培养组(共培养组)、共培养细胞+正常血清组、共培养细胞+含最佳药物血清组、siRNA FTO+正常血清组、siRNA FTO- nc +正常血清组、siRNA FTO+含最佳药物血清组。检测共培养细胞的活力和细胞周期变化。免疫荧光染色法检测归巢骨髓间充质干细胞水平及标志物。采用qRT-PCR检测Notch1通路相关基因的表达。Western blot检测Notch1通路相关蛋白的表达。结果与支气管上皮细胞组相比,共培养细胞组BMSCs归巢水平升高,C-X-C基序趋化因子受体4 (CXCR4)、基质细胞衍生因子1 (SDF-1)、Notch1、转录因子重组信号结合蛋白- j (RBP-J)、毛状分裂增强子1 (Hes1)蛋白表达增加。与共培养细胞组和共培养细胞+正常血清组相比,共培养细胞+含最佳药物血清组BMSCs归巢水平升高,CXCR4和SDF-1表达升高,Notch1和Hes1蛋白和mRNA水平降低。与siRNA FTO- nc +正常血清组比较,siRNA FTO+正常血清组Notch1、活化Notch1、RBP-J、Hes1蛋白水平升高,细胞活力升高,归巢BMSC水平降低。与siRNA FTO+正常血清组比较,含最佳药物siRNA FTO+血清中Notch1、RBP-J mRNA、活化Notch1、Hes1蛋白水平降低,归巢BMSCs水平升高。共培养细胞+含最佳药物组Notch1、RBP-J、Hes1 mRNA水平降低。与siRNA FTO+含最佳药物血清组相比,共培养细胞+含最佳药物血清组Notch1、活化Notch1、RBP-J、Hes1蛋白表达降低,细胞活力降低,归巢BMSCs水平升高。结论养和平喘颗粒可能通过上调FTO的表达,抑制Notch1信号通路下游基因的表达,促进BMSCs在哮喘中的归巢,减轻哮喘炎症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Observation of the effect of Yanghe Pingchuan granules on the homing of BMSCs in asthma based on FTO regulation of Notch1 pathway].

Objective To observe the effect of m6A methylation regulation on Notch1 pathway on the homing of BMSCs in asthma, and the intervention study of traditional Chinese medicine compound Yanghe Pingchuan Granules. Methods Rat bone mesenchymal stem cells(BMSC)and bronchial epithelial cells were cocultured. The extracted cells were divided into: bronchial epithelial cell group, asthma bronchial epithelial cell+mesenchymal stem cell co-culture group (co-culture group), co-culture cell+normal serum group, coculture cell+serum containing optimal drug group, siRNA FTO+normal serum group, siRNA FTO-NC+normal serum group, and siRNA FTO+serum containing optimal drug group. The vitality and cell cycle changes of co-cultured cells were detected. The level and markers of homing BMSC were detected by immunofluorescence staining. The expression of Notch1 pathway related genes were detected by qRT-PCR. The expression of Notch1 pathway related proteins were detected by Western blot. Results Compared with bronchial epithelial cell group, the co-cultured cell group showed an increase in the homing level of BMSCs and the expression of C-X-C motif chemokine receptor 4 (CXCR4), stromal cell-derived factor 1 (SDF-1), Notch1, transcription factor recombination signal binding protein-J (RBP-J), and hairy enhancer of split 1 (Hes1) proteins. Compared with the co-cultured cell group and co-cultured cell+normal serum group, the co-cultured cell+serum containing optimal drug group showed an increase in the homing level of BMSCs and the expressions of CXCR4 and SDF-1, while the protein and mRNA levels of Notch1 and Hes1 decreased. Compared with the siRNA FTO-NC+normal serum group, the siRNA FTO+normal serum group showed an increase in the levels of Notch1, activated Notch1, RBP-J, Hes1 protein, and cell viability, while the level of homing BMSC decreased. Compared with siRNA FTO+normal serum group, the levels of Notch1, RBP-J mRNA, activated Notch1, and Hes1 protein decreased, while the level of homing BMSCs increased in siRNA FTO+serum containing optimal drug group. The levels of Notch1, RBP-J, and Hes1 mRNA were reduced in the co-cultured cells+serum containing optimal drug group. Compared with siRNA FTO+serum containing optimal drug group, the expressions of Notch1, activated Notch1, RBP-J, Hes1 protein and cell viability decreased, while the level of homing BMSCs increased in the co-cultured cells+serum containing optimal drug group. Conclusion Yanghe Pingchuan Granules may promote the homing of BMSCs in asthma and alleviate asthma inflammation by upregulating the expression of FTO and inhibiting the expression of downstream genes in the Notch1 signaling pathway.

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