Faculty of Medicine, Pharmacology & Experimental Therapeutics Unit, Institute for Drug Research, School of Pharmacy, The Hebrew University of Jerusalem, Jerusalem, Israel.
Allergy. 2016 Jun;71(6):829-39. doi: 10.1111/all.12851. Epub 2016 Feb 26.
Staphylococcus aureus, one of the most important pathogens, is heavily associated with allergy. S. aureus and its toxins interact with eosinophils through CD48, a GPI-anchored receptor important in allergy mainly as expressed by the eosinophils (mCD48). CD48 can exist in a soluble form (sCD48). Our aim was to investigate SEB-induced regulation of eosinophil CD48 and the possible formation and role of sCD48 in SEB-mediated eosinophil activation in vitro and in vivo.
Human peripheral blood eosinophils were activated by SEB with or without inhibitors for phospholipases (PL) (-C or -D), or cycloheximide, or brefeldin A. We evaluated eosinophil activation (CD11b expression or EPO/IL-8 release), mCD48 (flow cytometry), sCD48 (ELISA), SEB binding to sCD48 (ELISA), and chemotaxis toward SEB. C57BL/6 mice were pre-injected (ip.) with sCD48, and then, peritonitis was induced by SEB injection; peritoneal lavages were collected after 48 h and analyzed by flow cytometry and ELISA.
SEB-activated human eosinophils formed sCD48, directly correlating with CD11b expression, through cell-associated PL-C and -D. mCD48 remained stable due to up-regulation in CD48 transcription and cellular trafficking. sCD48 bound to SEB and down-regulated SEB stimulatory effects on eosinophils as assessed by EPO and IL-8 release and eosinophil chemotaxis toward SEB. sCD48 showed anti-inflammatory activity in a SEB-induced mouse peritonitis model.
SEB regulates CD48 dynamics on eosinophils. Our data indicate sCD48 as a SEB-induced 'decoy' receptor derived from eosinophil and therefore as a potential anti-inflammatory tool in S. aureus-induced eosinophil inflammation often associated with allergy.
金黄色葡萄球菌是最重要的病原体之一,与过敏密切相关。金黄色葡萄球菌及其毒素通过 CD48 与嗜酸性粒细胞相互作用,CD48 是一种重要的 GPI 锚定受体,在过敏中主要由嗜酸性粒细胞(mCD48)表达。CD48 可以以可溶性形式(sCD48)存在。我们的目的是研究 SEB 诱导的嗜酸性粒细胞 CD48 调节以及 sCD48 在 SEB 介导的嗜酸性粒细胞体外和体内激活中的可能形成和作用。
用 SEB 激活人外周血嗜酸性粒细胞,有或没有磷脂酶(PL)(-C 或 -D)、环己酰亚胺或布雷菲德菌素 A 的抑制剂。我们评估嗜酸性粒细胞的激活(CD11b 表达或 EPO/IL-8 释放)、mCD48(流式细胞术)、sCD48(ELISA)、SEB 与 sCD48 的结合(ELISA)以及向 SEB 的趋化性。C57BL/6 小鼠预先用 sCD48 注射(ip.),然后用 SEB 注射诱导腹膜炎;48 小时后收集腹腔灌洗液,通过流式细胞术和 ELISA 进行分析。
SEB 激活的人嗜酸性粒细胞通过细胞相关的 PL-C 和 -D 形成 sCD48,与 CD11b 表达直接相关。由于 CD48 转录和细胞转运的上调,mCD48 保持稳定。sCD48 与 SEB 结合,并通过 EPO 和 IL-8 释放以及嗜酸性粒细胞向 SEB 的趋化性来下调 SEB 对嗜酸性粒细胞的刺激作用。sCD48 在 SEB 诱导的小鼠腹膜炎模型中显示出抗炎活性。
SEB 调节嗜酸性粒细胞上 CD48 的动态。我们的数据表明,sCD48 是 SEB 诱导的一种“诱饵”受体,来源于嗜酸性粒细胞,因此可能成为金黄色葡萄球菌诱导的嗜酸性粒细胞炎症的潜在抗炎工具,这种炎症通常与过敏有关。