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防风提取物对IgE致敏肥大细胞的改善作用及机制研究

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[目的]探究防风(Saposhnikovia divaricata,SD)提取物对大鼠嗜碱性白血病细胞RBL-2H3脱颗粒的影响及作用机制.[方法]采用噻唑蓝(methylthialazole tetrazolium,MTT)比色法检测,根据5、25、50、100、200、400 μg·mL-1SD提取物对RBL-2H3 细胞活性的影响,确定后续实验浓度.以免疫球蛋白E(immunoglobulinE,IgE)诱导建立RBL-2H3细胞脱颗粒模型.设立空白对照组、模型组、低剂量SD提取物组(5 μg·mL-1)、中剂量SD提取物组(25 μg·mL-1)、高剂量SD提取物组(50 μg·mL-1)和地塞米松(dexamethasone,DXMS)组(100 μg·mL1),干预30 min.MTT法检测低、中、高剂量SD提取物对RBL-2H3细胞脱颗粒模型活性的影响.甲苯胺蓝染色观察脱颗粒细胞形态,计算细胞脱颗粒率.免疫荧光染色测定细胞F-肌动蛋白(F-actin)表达.酶联免疫吸附试验(enzyme linked immunosorbent assay,ELISA)检测细胞β-氨基己糖苷酶、组胺、白细胞介素-4(interleukin-4,IL-4)、白细胞介素-6(interleukin-6,IL-6)、肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)、干扰素-γ(interferon-γ,IFN-γ)水平.免疫印迹法检测细胞磷脂酰肌醇-3-羟基激酶(phosphoinositide-3 kinase,PI3K)、磷酸化-PI3K(phosphorylation-PI3K,p-PI3K)、蛋白激酶 B(protein kinase B,AKT)、磷酸化-AKT(phosphorylation-AKT,p-AKT)、p38 丝裂原 活化蛋 白激酶(p3 8 mitogen activited protein kinaseelisa,p38MAPK)、磷酸化-p38MAPK(phosphorylation-p38MAPK,p-p38MAPK)、核因子-κB(nuclear factor-κB,NF-κB)、磷酸化-NF-κB(phosphorylation-NF-κB,p-NF-κB)、细胞外调节激酶(extracellular regulated kinases,ERK)、磷酸化-ERK(phosphorylation-ERK,p-ERK)蛋白表达.[结果]低、中、高剂量防风提取物(5、25、50 μg·mL-1)对RBL-2H3细胞活性无显著影响(P>0.05).与空白对照组比较,模型组甲苯胺蓝染色细胞数量减少、形态变圆,细胞脱颗粒率显著上升,F-actin表达下降,β-氨基己糖苷酶、组胺、IL-4、IL-6、TNF-α 水平升高,IFN-γ 水平降低,p-PI3K/PI3K、p-AKT/AKT、p-p38MAPK/p38MAPK、p-NF-KB/NF-KB、p-ERK/ERK表达升高(P<0.01).与模型组比较,低、中、高剂量SD提取物组和DXMS组细胞F-actin表达增加,β-氨基己糖苷酶、组胺、IL-4、IL-6、TNF-α 释放显著下降(P<0.05,P<0.01),IFN-γ 释放显著增加(P<0.01),p-PI3K/PI3K、p-AKT/AKT、p-p38MAPK/p38MAPK、p-NF-κB/NF-κB、p-ERK/ERK表达降低(P<0.05,P<0.01);中、高剂量SD提取物组和 DXMS组细胞数量增加,形态多呈梭形,细胞脱颗粒率显著下降(P<0.01).与低剂量SD提取物组比较,高剂量SD提取物组和DXMS组细胞脱颗粒率下降(P<0.01)、F-actin表达增加(P<0.05)、p-p38MAPK/p38MAPK表达降低(P<0.01).[结论]SD提取物可抑制 IgE 致敏的 RBL-2H3细胞脱颗粒,降低炎性介质水平,其作用机制可能与抑制PI3K/AKT、p38MAPK/NF-κB、ERK蛋白磷酸化有关.
Study of Improvement Effects and Mechanism of Saposhnikovia Divaricata Extract on IgE Sensitized RBL-2H3 Cells
[Objective]To explore the degranulation effect and mechanism of Saposhnikovia divaricata(SD)extract on rat basophilic leukemia cell line RBL-2H3 cell.[Methods]Methylthialazole tetrazolium(MTT)test was used to select the concentrations in the subsequent experiments based on impact of 5,25,50,100,200,400 μg·mL-1 SD extract on the activity of RBL-2H3 cells.Immunoglobulin E(IgE)induction was used to establish RBL-2H3 cell degranulation model.Blank control group,model group,low dose SD extract group(5 μg·mL-1),medium dose SD extract group(25 μg·mL-1),high dose SD extract group(50 μg·mL-1)and dexamethasone(DXMS)group(100 μg·mL-1)were set up,with intervention for 30 minutes.MTT test was used to detect the effect of low,medium,high-dose SD extract on activity of RBL-2H3 cell degranulation model.Toluidine blue staining was used to observe the morphology of degranulation cells and calculate degranulation rates.Immunofluorescence staining was used to detect expression of F-actin.Enzyme linked immunosorbent assay(ELISA)was used to detect the levels of β-aminohexosidase,histamine,interleukin-4(IL-4),interleukin-6(IL-6),tumor necrosis factor-α(TNF-α),interferon-γ(IFN-γ).Western blot was used to detect the expressions of phosphatidylinositide-3 kinase(PI3K),phosphorylation-PI3K(p-PI3K),protein kinase B(AKT),phosphorylation-AKT(p-AKT),p38 mitogen activated protein kinase(p38MAPK),phosphorylation-p38MAPK(p-p38MAPK),nuclear factors-κB(NF-κB),phosphorylation-NF-κB(p-NF-κB),extracellular regulated kinases(ERK)and phosphorylation-ERK(p-ERK)protein.[Results]The low,medium,high doses of SD extract(5,25,50 μg·mL-1)had no significant effects on the activity of RBL-2H3 cells(P>0.05).Compared with blank control group,the number of toluidine blue stained cells of model group was decreased,cells shape rounded,degranulation rate was increased,expression of F-actin was decreased,the levels of β-aminohexosidase,histamine,IL-4,IL-6,TNF-α were increased,IFN-γ level was decreased,the expressions of p-PI3K/PI3K,p-AKT/AKT,p-p38MAPK/p38MAPK,p-NF-κB/NF-κB and p-ERK/ERK were increased(P<0.01).Compared with model group,the F-actin expression of low,medium,high doses of SD extract groups and DXMS group was increased,levels of β-aminohexosidase,histamine,IL-4,IL-6 and TNF-α were decreased,IFN-γ level was increased(P<0.01),the expressions of p-PI3K/PI3K,p-AKT/AKT,p-p38MAPK/p38MAPK,p-NF-κB/NF-κB and p-ERK/ERK were decreased(P<0.05,P<0.01);the number of toluidine blue stained cells in medium,high dose SD extract groups and DXMS group was increased with spindle cell shape,degranulation rate was decreased(P<0.01).Compared with low dose SD extract group,degranulation rate of high dose SD extract group and DXMS group was decreased(P<0.01),F-actin expression was increased(P<0.05),p-p38MAPK/p38MAPK expressions were decreased(P<0.01).[Conclusion]SD extract inhibited degranulation of IgE sensitized RBL-2H3 cell and decreased the levels of inflammatory mediators,its mechanism may be related to the inhibition the phosphorylation expression of PI3K/AKT,p38MAPK/NF-KB and ERK.

Saposhnikovia divaricata extractRBL-2H3 cellcell degranulationF-actinhistamineinflammatory factors

陈思思、钱丽梅、陈艳春

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湖州市第三人民医院 浙江,湖州 313000

杭州市第七人民医院

杭州市中医院

防风提取物 RBL-2H3细胞 细胞脱颗粒 F-肌动蛋白 组胺 炎症因子

浙江省中医药管理局项目杭州市科技发展计划项目湖州市科学技术局公益性应用研究项目

2021ZA10420201203B2162019GY06

2024

浙江中医药大学学报
浙江中医药大学

浙江中医药大学学报

CSTPCD
影响因子:1.049
ISSN:1005-5509
年,卷(期):2024.48(2)
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