Department of Molecular and Cellular Biology, Roswell Park Cancer Institute, Buffalo, New York, USA.
J Leukoc Biol. 2010 Mar;87(3):457-66. doi: 10.1189/jlb.1108704. Epub 2009 Dec 9.
Cumulative evidence indicates that the sialyltransferase ST6Gal-1 and the sialyl-glycans, which it constructs, are functionally pleiotropic. Expression of the ST6Gal-1 gene is mediated by six distinct promoter/regulatory regions, and we hypothesized that these promoters may be used differentially to produce ST6Gal-1 for different biologic purposes. To examine this hypothesis, we compared a mouse with a complete deficiency in ST6Gal-1 (Siat1 null) with another mouse that we have created previously with a disruption only in the P1 promoter (Siat1DeltaP1). We noted previously greater neutrophilic inflammation associated with ST6Gal-1 deficiency. Here, we report that ST6Gal-1-deficient mice also have significantly elevated eosinophilic responses. Upon i.p. thioglycollate elicitation, eosinophils accounted for over 20% of the total peritoneal inflammatory cell pool in ST6Gal-1-deficient animals, which was threefold greater than in corresponding wild-type animals. A principal feature of allergic respiratory inflammation is pulmonary eosinophilia, we evaluated the role of ST6Gal-1 in allergic lung inflammation. Using OVA and ABPA experimental models of allergic airways, we showed that ST6Gal-1 deficiency led to greater airway inflammation characterized by excessive airway eosinophilia. The severity of airway inflammation was similar between Siat1DeltaP1 and Siat1 null mice, indicating a role for P1-generated ST6Gal-1 in regulating eosinophilic inflammation. Colony-forming assays suggested greater IL-5-dependent eosinophil progenitor numbers in the marrow of ST6Gal-1-deficient animals. Moreover, allergen provocation of wild-type mice led to a significant reduction in P1-mediated ST6Gal-1 mRNA and accompanied decline in circulatory ST6Gal-1 levels. Taken together, the data implicate ST6Gal-1 as a participant in regulating not only Th1 but also Th2 responses, and ST6Gal-1 deficiency can lead to the development of more severe allergic inflammation with excessive eosinophil production.
累积的证据表明,唾液酸转移酶 ST6Gal-1 和它构建的唾液酸化聚糖在功能上是多功能的。ST6Gal-1 基因的表达受六个不同的启动子/调节区域介导,我们假设这些启动子可能会被不同地用于产生 ST6Gal-1,以达到不同的生物学目的。为了检验这一假设,我们比较了一种 ST6Gal-1 完全缺乏的小鼠(Siat1 基因敲除)和我们之前创建的另一种仅在 P1 启动子处发生破坏的小鼠(Siat1DeltaP1)。我们之前曾注意到 ST6Gal-1 缺乏与中性粒细胞炎症增加有关。在这里,我们报告 ST6Gal-1 缺乏的小鼠也有明显升高的嗜酸性粒细胞反应。在腹腔注射硫代乙醇酸引发后,ST6Gal-1 缺乏的动物腹腔内炎症细胞池中嗜酸性粒细胞占比超过 20%,是相应野生型动物的三倍。过敏呼吸炎症的一个主要特征是肺部嗜酸性粒细胞增多,我们评估了 ST6Gal-1 在过敏性肺炎症中的作用。使用 OVA 和 ABPA 过敏性气道模型,我们表明 ST6Gal-1 缺乏导致更严重的气道炎症,表现为过度的气道嗜酸性粒细胞增多。Siat1DeltaP1 和 Siat1 基因敲除小鼠之间气道炎症的严重程度相似,表明 P1 生成的 ST6Gal-1 在调节嗜酸性粒细胞炎症中起作用。集落形成实验表明,ST6Gal-1 缺乏的动物骨髓中 IL-5 依赖性嗜酸性粒细胞前体数量增加。此外,过敏原刺激野生型小鼠导致 P1 介导的 ST6Gal-1 mRNA 显著减少,并伴有循环 ST6Gal-1 水平下降。总之,这些数据表明 ST6Gal-1 不仅参与调节 Th1 反应,还参与调节 Th2 反应,ST6Gal-1 缺乏可导致更严重的过敏炎症,产生过多的嗜酸性粒细胞。