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Integrin alpha 4 beta 7 mediates human eosinophil interaction with MAdCAM-1, VCAM-1 and fibronectin.

机译:整合素α4 beta 7介导人嗜酸性粒细胞与MAdCAM-1,VCAM-1和纤连蛋白的相互作用。

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摘要

We have investigated the contribution of integrin alpha 4 beta 7 to human peripheral blood eosinophil adhesive interactions. Immunofluorescence and flow cytometry demonstrated constitutive expression of alpha 4 beta 7 by eosinophils. Expression of alpha 4 beta 7 or alpha 4 beta 7 was not enhanced by eosinophil activation with platelet-activating factor (PAF). Expression of alpha 4 beta 7 was confirmed by immuno-precipitation of 125I-labeled lysates analysed by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS PAGE). Approximately 20% of unstimulated eosinophils were adherent to L1-2 cells transfected with vascular cell adhesion molecule-1 (VCAM-1) cDNA, while very few resting eosinophils adhered to mouse mucosal adressin cell adhesion molecule-1 (MAdCAM-1) transfectants. Binding of unstimulated eosinophils to VCAM-1 transfectant was inhibited by HPI 2 (an antibody that blocks both alpha 4 beta 1 and alpha 4 beta 7 functions), but not Act-1, and alpha 4 beta 1 monoclonal antibody (mAb). PAF stimulation resulted in increased binding of eosinophils to MAdCAM-1 transfectants, which was inhibited by both HPI 2 and Act-1. In contrast, PAF did not enhance binding to VCAM 1 transfectants, although binding of PAE-stimulated eosinophils to VCAM-1 could be partially inhibited by Act-1. Stimulation of eosinophils with the beta 7-activating mAb TS2 16 resulted in enhanced binding of eosinophils to both VCAM-1 and MAdCAM-1 transfectants. The increased binding was largely alpha 4 beta 7-dependent. Unstimulated eosinophils bound to soluble recombinant human (rh) VCAM-1 and fibronectin (Fn), coated on 96-well plates in dose-dependent manner. Binding was inhibited by HPI-2 and 4b4, an anti-beta 1 mAb, but not by Act-1. TS2 16 treatment increased adherent cell numbers and this enhanced binding was inhibited by Act-1. We have therefore confirmed that alpha 4 beta 7 is functionally active on unstimulated eosinophils. In contrast, PAF-induced enhancement of eosinophils binding to VCAM-1 or MAdCAM-1 was alpha 4 beta 7-dependent. In addition treatment with TS2 16 resulted in a alpha 4 beta 7-dependent enhancement of eosinophil binding to VCAM-1, MAdCAM-1 and Fn. We therefore hypothesize that alpha 4 beta 7 may have an important role in eosinophil localization in diseases such as asthma and inflammatory bowel disease.
机译:我们已经调查了整合素α4 beta 7对人类外周血嗜酸性粒细胞粘附相互作用的贡献。免疫荧光和流式细胞仪证实嗜酸性粒细胞组成性表达α4 beta 7。血小板活化因子(PAF)激活嗜酸性粒细胞并没有增强alpha 4 beta 7或alpha 4 beta 7的表达。通过用十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS PAGE)分析125 I标记的裂解物进行免疫沉淀,确认了α4 beta 7的表达。大约20%的未刺激嗜酸性粒细胞粘附到被血管细胞粘附分子1(VCAM-1)cDNA转染的L1-2细胞上,而几乎没有静止的嗜酸性粒细胞粘附到小鼠粘膜阿奇霉素细胞粘附分子1(MAdCAM-1)转染子上。未刺激的嗜酸性粒细胞与VCAM-1转染子的结合受到HPI 2(一种同时阻断alpha 4 beta 1和alpha 4 beta 7功能的抗体)的抑制,但没有抑制Act-1和alpha 4 beta 1单克隆抗体(mAb)。 PAF刺激导致嗜酸性粒细胞与MAdCAM-1转染子的结合增加,这被HPI 2和Act-1抑制。相反,尽管PAE刺激的嗜酸性粒细胞与VCAM-1的结合可能被Act-1部分抑制,但PAF并未增强与VCAM 1转染子的结合。用激活β7的mAb TS2 16刺激嗜酸性粒细胞可增强嗜酸性粒细胞与VCAM-1和MAdCAM-1转染子的结合。增加的结合主要是α4β7依赖性的。未刺激的嗜酸性粒细胞与可溶性重组人(rh)VCAM-1和纤连蛋白(Fn)结合,并以剂量​​依赖性方式包被在96孔板上。结合被HPI-2和抗β1mAb 4b4抑制,但不受Act-1抑制。 TS2 16处理增加了粘附细胞的数量,而这种增强的结合被Act-1抑制。因此,我们证实了α4beta 7在未刺激的嗜酸性粒细胞上具有功能活性。相反,PAF诱导的嗜酸性粒细胞与VCAM-1或MAdCAM-1结合的增强是α4beta 7依赖性的。另外,用TS2 16处理导致嗜酸性粒细胞与VCAM-1,MAdCAM-1和Fn结合的α4β7依赖性增强。因此,我们假设alpha 4 beta 7可能在哮喘和炎症性肠病等疾病的嗜酸性粒细胞定位中起重要作用。

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