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季节性变应性鼻炎患者胱抑素 SN 的上调。

Cystatin SN upregulation in patients with seasonal allergic rhinitis.

机构信息

Department of Otorhinolaryngology Head & Neck Surgery, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.

出版信息

PLoS One. 2013 Aug 12;8(8):e67057. doi: 10.1371/journal.pone.0067057. eCollection 2013.

Abstract

Seasonal allergic rhinitis (SAR) to the Japanese cedar, Cryptomeria japonica (JC) pollen is an IgE-mediated type I allergy affecting nasal mucosa. However, the molecular events underlying its development remain unclear. We sought to identify SAR-associated altered gene expression in nasal epithelial cells during natural exposure to JC pollen. We recruited study participants in 2009 and 2010 and collected nasal epithelial cells between February and April, which is the period of natural pollen dispersion. Fifteen patients with SAR-JC and 13 control subjects were enrolled in 2009, and 17 SAR-JC patients, 13 sensitized asymptomatic subjects (Sensitized), and 15 control subjects were enrolled in 2010. Total RNA was extracted from nasal epithelial cells and 8 SAR-JC patients and 6 control subjects in 2009 were subjected to microarray analysis with the Illumina HumanRef-8 Expression BeadChip platform. Allergen-stimulated histamine release was examined in the peripheral blood basophils isolated from patients with SAR. We identified 32 genes with significantly altered expression during allergen exposure. One of these, CST1 encodes the cysteine protease inhibitor, cystatin SN. CST1 expression in nasal epithelial cells was significantly upregulated in both the 2009 and 2010 SAR-JC groups compared with the control groups. Immunohistochemical staining confirmed the increased expression of CST1 in the nasal epithelial cells of SAR patients. Addition of exogenous CST1 to basophils inhibited JC allergen-stimulated histamine release in vitro. We propose that CST1 may contribute to inactivation of protease allergens and help re-establish homeostasis of the nasal membranes.

摘要

季节性过敏性鼻炎(SAR)对日本雪松(Cryptomeria japonica,JC)花粉是一种 IgE 介导的 I 型过敏,影响鼻黏膜。然而,其发病机制的分子事件尚不清楚。我们试图在鼻上皮细胞自然暴露于 JC 花粉时识别与 SAR 相关的改变的基因表达。我们于 2009 年和 2010 年招募了研究参与者,并在 2 月至 4 月期间采集鼻上皮细胞,这是自然花粉扩散的时期。2009 年共纳入 15 例 SAR-JC 患者和 13 例对照者,17 例 SAR-JC 患者、13 例致敏无症状者(致敏)和 15 例对照者于 2010 年纳入研究。从鼻上皮细胞中提取总 RNA,并对 2009 年的 8 例 SAR-JC 患者和 6 例对照者进行 Illumina HumanRef-8 Expression BeadChip 平台的微阵列分析。从 SAR 患者外周血嗜碱性粒细胞中检测变应原刺激的组胺释放。我们鉴定了 32 个在变应原暴露过程中表达明显改变的基因。其中之一,CST1 编码半胱氨酸蛋白酶抑制剂胱抑素 SN。与对照组相比,2009 年和 2010 年 SAR-JC 组鼻上皮细胞 CST1 的表达均显著上调。免疫组织化学染色证实了 SAR 患者鼻上皮细胞 CST1 表达增加。外源性 CST1 加入嗜碱性粒细胞可抑制 JC 变应原刺激的组胺释放。我们提出 CST1 可能有助于蛋白酶过敏原的失活,并有助于重建鼻膜的内稳态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c82b/3741298/d8b1a901367e/pone.0067057.g001.jpg

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