Hayakawa Hiroko, Hayakawa Morisada, Tominaga Shin-Ichi
Department of Biochemistry, Jichi Medical University, 3311-1 Yakushiji, Shimotsuke-shi, Tochigi 329-0498, Japan.
Biochem Biophys Rep. 2016 Feb 3;5:401-407. doi: 10.1016/j.bbrep.2016.02.002. eCollection 2016 Mar.
Type 2 innate lymphoid cells (ILC2) in lungs produce interleukin (IL)-5 and IL-13 in response to IL-33 and may contribute to the development of allergic diseases such as asthma. However, little is known about negative regulators and effective inhibitors controlling ILC2 function. Here, we show that soluble ST2, a member of the IL-1 receptor family, suppresses the effect of IL-33 on lung ILC2 . Stimulation with IL-33 to naïve ILC2 induced morphological change and promoted cell proliferation. In addition, IL-33 upregulated expression of cell surface molecules including IL-33 receptor and induced production of IL-5 and IL-13, but not IL-4. Pretreatment with soluble ST2 suppressed IL-33-mediated responses of ILC2. The results suggest that soluble ST2 acts as a decoy receptor for IL-33 and protects ILC2 from IL-33 stimulation.
肺部的2型天然淋巴细胞(ILC2)在白细胞介素(IL)-33的作用下产生IL-5和IL-13,可能会导致哮喘等过敏性疾病的发生。然而,对于控制ILC2功能的负调节因子和有效抑制剂知之甚少。在这里,我们表明,可溶性ST2是IL-1受体家族的成员,可抑制IL-33对肺ILC2的作用。用IL-33刺激幼稚ILC2会诱导形态变化并促进细胞增殖。此外,IL-33上调包括IL-33受体在内的细胞表面分子的表达,并诱导IL-5和IL-13的产生,但不诱导IL-4的产生。用可溶性ST2预处理可抑制IL-33介导的ILC2反应。结果表明,可溶性ST2作为IL-33的诱饵受体,保护ILC2免受IL-33刺激。