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[基因芯片检测变应性鼻炎趋化因子及其受体基因表达的实验]

[Experiment of genes expression of chemokines and their receptors in allergic rhinitis with gene chip].

作者信息

Yu Shaoqing, Zhang Ruxin, Liu Guojun, Wen Wu, Shen Xiaohua

机构信息

Department of Otorhinolaryngology, Changhai Hospital, the Second Military University, Shanghai, 200433, China.

出版信息

Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2005 Jan;19(2):52-4.

Abstract

OBJECTIVE

To analyze the role of chemokines and their receptors in the mechanism of allergic rhinitis (AR) by observing the expression of genes of chemokines and their receptors in nasal mucosa of AR through gene chip.

METHOD

The total RNAs were isolated from nasal mucosa of AR and purified to mRNAs, then reversely transcribed to cDNAs and incorporated with fluorescent-labled CY5-dUPT for probes preparion. CY3-dUTP probes prepared with normal nasal mucosa of normal for control. The chip contains cDNAs of chemokines and their receptors were used to hybridized with probes then screened with computer to study the expression of genes based on different density of fluorescent.

RESULT

The chemokines of CCL11 (eotaxin-1), CCL24 (eotaxin-2), CCL7 (MCP-3), CCL13 (MCP-4), RANTES (CCL5) and receptors of CCR2, CCR3, CCR4, CCR5 were differential expressed on four samples, and most of the chemokines and their receptors has tendency regulation on T help 2 (Th2) lymphocytes and involved in the prodeeds such as inducement of allergic reaction,accumulation of inflammacytes and degranulation of sensitized cells.

CONCLUSION

A disorder exists in T helper immune system with AR. The chemokines and their receptors that polarized with Th2 lymphocytes perhaps play important roles in AR pathogenesis, and it represents a new approach to AR immunotherapy.

摘要

目的

通过基因芯片观察变应性鼻炎(AR)鼻黏膜趋化因子及其受体基因的表达,分析趋化因子及其受体在AR发病机制中的作用。

方法

从AR患者鼻黏膜中提取总RNA并纯化得到mRNA,然后逆转录成cDNA,与荧光标记的CY5-dUTP掺入用于探针制备。以正常鼻黏膜制备的CY3-dUTP探针作为对照。用含有趋化因子及其受体cDNA的芯片与探针杂交,然后用计算机根据荧光密度不同筛选,研究基因表达情况。

结果

CCL11(嗜酸性粒细胞趋化因子-1)、CCL24(嗜酸性粒细胞趋化因子-2)、CCL7(单核细胞趋化蛋白-3)、CCL13(单核细胞趋化蛋白-4)、RANTES(CCL5)等趋化因子以及CCR2、CCR3、CCR4、CCR5受体在4个样本中差异表达,且大多数趋化因子及其受体对辅助性T细胞2(Th2)淋巴细胞有趋势性调节作用,参与诱导过敏反应、炎症细胞聚集和致敏细胞脱颗粒等过程。

结论

AR患者存在辅助性T细胞免疫系统紊乱。与Th2淋巴细胞极化相关的趋化因子及其受体可能在AR发病机制中起重要作用,这为AR免疫治疗提供了新途径。

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