Kuperman Douglas A, Schleimer Robert P
Northwestern University Feinberg School of Medicine, Department of Medicine, Division of Allergy-Immunology, Chicago, Illinois 60611, USA.
Curr Mol Med. 2008 Aug;8(5):384-92. doi: 10.2174/156652408785161032.
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.
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。