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[微小RNA-20b对哮喘小鼠气道炎症的抑制作用]

[Inhibitory effect of miR-20b on airway inflammation in asthmatic mice].

作者信息

Ma Hua, Luo Yu-Lan, Guo Shu-Jun, Shen Lin, Song Chuan-Wang

机构信息

Department of Immunology, Anhui Provincial Key Laboratory of Infection and Immunity, Bengbu Medical College, Bengbu 233030, China. E-mail:

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2015 Oct;35(10):1463-6.

Abstract

OBJECTIVE

To explore the effect of miR-20b in inhibiting airway inflammation in a mouse model of asthma.

METHODS

Female BALB/c mouse models of asthma, established by sensitizing and challenging the mice with a mixture of ovalbumin and aluminum hydroxide, were subjected to intranasal instillation of 20 µg miR-20b mimics or a miR-20b scramble every 3 days. On day 49, bronchoalveolar lavage fluid (BALF) was collected from the mice to examine the counts of total cells and different cell populations; HE staining was used to observe the pathological changes of the lung tissue, and the concentration of vascular endothelial growth factor (VEGF) in BALF was detected by ELISA.

RESULTS

Treatment of the asthmatic mice with miR-20b mimics decreased not only the counts of the total leukocytes, neutrophils and eosinophils in the BALF but also mucus secretion in the airway and inflammatory cell infiltration around the bronchus, and lessened thickening of the airway mucosa. Instillation with miR-20b mimics significantly reduced the concentration of VEGF in BALF from 28.55±3.42 pg/mL in the asthma model group to 18.19±3.67 pg/mL (P<0.01).

CONCLUSION

MiR-20b can inhibit airway inflammation in asthmatic mice possibly by reducing the expression of VEGF.

摘要

目的

探讨miR - 20b在哮喘小鼠模型中抑制气道炎症的作用。

方法

用卵清蛋白和氢氧化铝混合物致敏并激发雌性BALB/c小鼠建立哮喘模型,每3天经鼻滴注20μg miR - 20b模拟物或miR - 20b乱序对照。在第49天,从小鼠收集支气管肺泡灌洗液(BALF)以检查总细胞数和不同细胞群体计数;采用苏木精 - 伊红(HE)染色观察肺组织的病理变化,并用酶联免疫吸附测定(ELISA)法检测BALF中血管内皮生长因子(VEGF)的浓度。

结果

用miR - 20b模拟物处理哮喘小鼠不仅降低了BALF中总白细胞、中性粒细胞和嗜酸性粒细胞的计数,还减少了气道黏液分泌和支气管周围的炎性细胞浸润,并减轻了气道黏膜增厚。滴注miR - 20b模拟物显著降低了BALF中VEGF的浓度,从哮喘模型组的28.55±3.42 pg/mL降至18.19±3.67 pg/mL(P<0.01)。

结论

MiR - 20b可能通过降低VEGF的表达来抑制哮喘小鼠的气道炎症。

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