实用医学杂志 ›› 2022, Vol. 38 ›› Issue (9): 1082-1087.doi: 10.3969/j.issn.1006⁃5725.2022.09.008

• 基础研究 • 上一篇    下一篇

AMD3100 干预CXCR4 对哮喘小鼠气道黏蛋白 MUC5ac 蛋白表达的影响

王莉 刘小静 张建勇   

  1. 贵州省遵义医科大学附属医院呼吸与危重症医学科(贵州遵义 563000)

  • 出版日期:2022-05-10 发布日期:2022-05-10
  • 通讯作者: 张建勇 E⁃mail:zjy9453@sina.com
  • 基金资助:
    贵州省科技厅资助项目(编号:黔科合支撑[2020]4Y162 号);遵义市科技厅(编号:遵市科合 HZ 字(2019)116 号)

Effects of AMD3100 intervention on CXCR4 and MUC5ac in asthmatic mice

WANG Li,LIU Xiaojing, ZHANG Jianyong.   

  1. Department of Respiratory and Critical Care Medicine,Affliated Hospital of Zunyi Medical Univer⁃ sity,Zunyi 563000,China

  • Online:2022-05-10 Published:2022-05-10
  • Contact: ZHANG Jianyong E⁃mail:zjy9453@sina.com

摘要:

目的 探讨 AMD3100(Plerixafor,普乐沙福)干预 CXCR4 对哮喘小鼠气道黏蛋白 MUC5ac 的影响及可能机制。方法 6 ~ 8 BALB/C 雌性小鼠分为正常组(NS 组)、哮喘组(AS 组)和 CXCR4 阻滞 AMD3100 组(AMD 组),各 8 只。卵清蛋白(OVA)致敏后,雾化吸入 OVA 激发制备哮喘模型,各组在激 发前进行干预。通过酶联免疫吸附法检测肺泡灌洗液中白细胞介素(IL)⁃4,IL⁃5 CXCR4,肺组织行 HE 染色、AB⁃PAS 染色观察肺组织病理学改变;免疫组织化学检测 CXCR4、气道 MUC5ac 蛋白表达变化,RT⁃ PCR 检测肺组织 CXCR4 mRNA 表达水平。结果 AMD3100 组小鼠 BALF IL⁃4、IL⁃5、CXCR4 水平、支气 管周围炎症病理评分、气道上皮杯状细胞和黏液物质阳性相对着色面积、肺组织 MUC5ac 蛋白、CXCR4 白表达及 CXCR4 mRNA 表达水平较哮喘组降低,但仍高于正常对照组(P < 0.05)。结论 AMD3100 干预 CXCR4 蛋白的表达,抑制哮喘小鼠气道炎症反应及下调 MUC5ac 的表达,减轻气道黏液高分泌,改善哮喘 症状。

关键词:

支气管哮喘, AMD3100, CXC 趋化因子受体4, MUC5ac 蛋白

Abstract:

Objective To explore the effect and mechanism of AMD3100 on CXCR4 and MUC5ac in asthma mice. Methods Female BALB/c mice aged to 6 ~ 8 weeks were randomly divided into normal group(NS group), asthma group(AS group),CXCR4 blockers group(AMD group),Eight in each group.Asthma was induced by OVA sensitization and challenge,intervention was performed in each group before stimulation. IL ⁃ 4,IL ⁃5,CXCR4 in BALF were detected by ELISA.The pathological changes of lung were observed by HE staining,AB ⁃PAS staining IHC and RT⁃PCR were used to detect the expression of Muc5ac,CXCR4 protein level and CXCR4 mRNA in lung tissues. Results The CXCR4,IL⁃4 and IL⁃5 levels,infiltration of inflammatory cells around the airway of lung tis⁃ sue,positive relative coloring area of airway mucus,CXCR4 and Muc5ac protein content,mRNA relative expression of CXCR4,AMD group were lower than AS group(P < 0.01). was higher than NS group(P < 0.05). Conclusions AMD3100 intervention can reduce the expression of CXCR4 protein,inhibits airway inflammatory and down regu⁃ lates the expression of MUC5AC in asthmatic mice,alleviate airway mucus hypersecretion,and improves asthmatic symptoms.

Key words:

bronchial asthma, AMD3100, CXC chemokine receptor 4, Mucin5AC