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本文引用的文献

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Cytokine-mediated control of lipopolysaccharide-induced activation of small intestinal epithelial cells.细胞因子介导的对脂多糖诱导的小肠上皮细胞激活的控制
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Central role of Muc5ac expression in mucous metaplasia and its regulation by conserved 5' elements.Muc5ac表达在黏液化生中的核心作用及其受保守5'元件的调控
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Nippostrongylus brasiliensis: identification of intelectin-1 and -2 as Stat6-dependent genes expressed in lung and intestine during infection.巴西日圆线虫:鉴定凝集素-1和-2为感染期间在肺和肠道中表达的Stat6依赖性基因。
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IL-13 blockade reduces lung inflammation after Ascaris suum challenge in cynomolgus monkeys.在食蟹猴受到猪蛔虫攻击后,白细胞介素-13阻断可减轻肺部炎症。
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SPDEF regulates goblet cell hyperplasia in the airway epithelium.SPDEF调节气道上皮中的杯状细胞增生。
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Influence of cigarette smoke on the arginine pathway in asthmatic airways: increased expression of arginase I.香烟烟雾对哮喘气道中精氨酸途径的影响:精氨酸酶I表达增加。
J Allergy Clin Immunol. 2007 Feb;119(2):391-7. doi: 10.1016/j.jaci.2006.10.030.
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Comparative roles of IL-4, IL-13, and IL-4Ralpha in dendritic cell maturation and CD4+ Th2 cell function.白细胞介素-4、白细胞介素-13和白细胞介素-4受体α在树突状细胞成熟和CD4+ Th2细胞功能中的比较作用。
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9
Allergen induced TFF2 is expressed by mucus-producing airway epithelial cells but is not a major regulator of inflammatory responses in the murine lung.变应原诱导的三叶因子2由产生黏液的气道上皮细胞表达,但不是小鼠肺中炎症反应的主要调节因子。
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10
Eosinophils and CCR3 regulate interleukin-13 transgene-induced pulmonary remodeling.嗜酸性粒细胞和CCR3调节白细胞介素-13转基因诱导的肺重塑。
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白细胞介素-4、白细胞介素-13、信号转导和转录激活因子6与过敏性哮喘

Interleukin-4, interleukin-13, signal transducer and activator of transcription factor 6, and allergic asthma.

作者信息

Kuperman Douglas A, Schleimer Robert P

机构信息

Northwestern University Feinberg School of Medicine, Department of Medicine, Division of Allergy-Immunology, Chicago, Illinois 60611, USA.

出版信息

Curr Mol Med. 2008 Aug;8(5):384-92. doi: 10.2174/156652408785161032.

DOI:10.2174/156652408785161032
PMID:18691065
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4437630/
Abstract

Interleukin (IL)-4 and IL-13 share many biological activities. To some extent, this is because they both signal via a shared receptor, IL-4Ralpha. Ligation of IL-4Ralpha results in activation of Signal Transducer and Activator of Transcription factor 6 (STAT6) and Insulin Receptor Substrate (IRS) molecules. In T- and B-cells, IL-4Ralpha signaling contributes to cell-mediated and humoral aspects of allergic inflammation. It has recently become clear that IL-4 and IL-13 produced in inflamed tissues activate signaling in normally resident cells of the airway. The purpose of this review is to critically evaluate the contributions of IL-4- and IL-13-induced tissue responses, especially those mediated by STAT6, to some of the pathologic features of asthma including eosinophilic inflammation, airway hyperresponsiveness, subepithelial fibrosis and excessive mucus production. We also review the functions of some recently identified IL-4- and/or IL-13-induced mediators that provide some detail on molecular mechanisms and suggest an important contribution to host defense.

摘要

白细胞介素(IL)-4和IL-13具有许多共同的生物学活性。在某种程度上,这是因为它们都通过共同的受体IL-4Rα进行信号传导。IL-4Rα的结合会导致信号转导和转录激活因子6(STAT6)以及胰岛素受体底物(IRS)分子的激活。在T细胞和B细胞中,IL-4Rα信号传导有助于过敏性炎症的细胞介导和体液方面。最近已经明确,炎症组织中产生的IL-4和IL-13可激活气道正常驻留细胞中的信号传导。本综述的目的是批判性地评估IL-4和IL-13诱导的组织反应,特别是那些由STAT6介导的反应,对哮喘的一些病理特征的贡献,包括嗜酸性粒细胞炎症、气道高反应性、上皮下纤维化和黏液过度分泌。我们还综述了一些最近发现的IL-4和/或IL-13诱导的介质的功能,这些介质详细阐述了分子机制,并表明对宿主防御有重要贡献。