Division of Allergy-Immunology, Northwestern Univeristy Feinberg School of Medicine, Chicago, IL 60611, USA.
Am J Physiol Lung Cell Mol Physiol. 2012 Oct 15;303(8):L642-60. doi: 10.1152/ajplung.00406.2011. Epub 2012 Jul 27.
Clinical reports indicate that patients with allergy/asthma commonly have associated symptoms of anxiety/depression. Anxiety/depression can be reduced by 5-hydroxytryptophan (5-HTP) supplementation. However, it is not known whether 5-HTP reduces allergic inflammation. Therefore, we determined whether 5-HTP supplementation reduces allergic inflammation. We also determined whether 5-HTP decreases passage of leukocytes through the endothelial barrier by regulating endothelial cell function. For these studies, C57BL/6 mice were supplemented with 5-HTP, treated with ovalbumin fraction V (OVA), house dust mite (HDM) extract, or IL-4, and examined for allergic lung inflammation and OVA-induced airway responsiveness. To determine whether 5-HTP reduces leukocyte or eosinophil transendothelial migration, endothelial cells were pretreated with 5-HTP, washed and then used in an in vitro transendothelial migration assay under laminar flow. Interestingly, 5-HTP reduced allergic lung inflammation by 70-90% and reduced antigen-induced airway responsiveness without affecting body weight, blood eosinophils, cytokines, or chemokines. 5-HTP reduced allergen-induced transglutaminase 2 (TG2) expression and serotonylation (serotonin conjugation to proteins) in lung endothelial cells. Consistent with the regulation of endothelial serotonylation in vivo, in vitro pretreatment of endothelial cells with 5-HTP reduced TNF-α-induced endothelial cell serotonylation and reduced leukocyte transendothelial migration. Furthermore, eosinophil and leukocyte transendothelial migration was reduced by inhibitors of transglutaminase and by inhibition of endothelial cell serotonin synthesis, suggesting that endothelial cell serotonylation is key for leukocyte transendothelial migration. In summary, 5-HTP supplementation inhibits endothelial serotonylation, leukocyte recruitment, and allergic inflammation. These data identify novel potential targets for intervention in allergy/asthma.
临床报告表明,过敏/哮喘患者常伴有焦虑/抑郁等相关症状。5-羟色氨酸(5-HTP)补充剂可以减轻焦虑/抑郁症状。然而,目前尚不清楚 5-HTP 是否可以减轻过敏炎症。因此,我们旨在确定 5-HTP 补充剂是否可以减轻过敏炎症。我们还旨在确定 5-HTP 是否通过调节内皮细胞功能来减少白细胞通过内皮屏障的迁移。为此,我们用 5-HTP 处理 C57BL/6 小鼠,用卵清蛋白第五部分(OVA)、屋尘螨(HDM)提取物或白细胞介素 4(IL-4)处理,观察过敏肺炎症和 OVA 诱导的气道反应性。为了确定 5-HTP 是否减少白细胞或嗜酸性粒细胞的跨内皮迁移,我们先用 5-HTP 预处理内皮细胞,然后用清洗液清洗,再在层流条件下进行体外跨内皮迁移试验。有趣的是,5-HTP 可使过敏肺炎症减轻 70%-90%,并降低抗原诱导的气道反应性,而不影响体重、血液嗜酸性粒细胞、细胞因子或趋化因子。5-HTP 减少了肺内皮细胞中的过敏原诱导的转谷氨酰胺酶 2(TG2)表达和血清素化(血清素与蛋白质的结合)。与体内内皮细胞的血清素化调节一致,5-HTP 预处理内皮细胞可减少 TNF-α诱导的内皮细胞血清素化,并减少白细胞的跨内皮迁移。此外,抑制转谷氨酰胺酶和抑制内皮细胞血清素合成可减少嗜酸性粒细胞和白细胞的跨内皮迁移,表明内皮细胞的血清素化是白细胞跨内皮迁移的关键。总之,5-HTP 补充剂抑制内皮细胞的血清素化、白细胞募集和过敏炎症。这些数据为过敏/哮喘的干预提供了新的潜在靶点。