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一种新型的CRTH2拮抗剂可阻断嗜酸性粒细胞从骨髓的释放、趋化作用和呼吸爆发。

A novel antagonist of CRTH2 blocks eosinophil release from bone marrow, chemotaxis and respiratory burst.

作者信息

Royer J F, Schratl P, Lorenz S, Kostenis E, Ulven T, Schuligoi R, Peskar B A, Heinemann A

机构信息

Institute of Experimental and Clinical Pharmacology, Medical University of Graz, Graz, Austria.

出版信息

Allergy. 2007 Dec;62(12):1401-9. doi: 10.1111/j.1398-9995.2007.01452.x. Epub 2007 Aug 21.

Abstract

BACKGROUND

Chemoattractant receptor-homologous molecule expressed on Th2 cells (CRTH2) has been revealed to be a novel receptor for prostaglandin (PG) D(2), which is a major mast cell product released during the allergic response. The aim of this study was to analyze the effects of a newly developed small molecule antagonist of CRTH2, Cay10471, on eosinophil function with respect to recruitment, respiratory burst and degranulation.

METHODS

Chemotaxis of guinea pig bone marrow eosinophils and human peripheral blood eosinophils were determined using microBoyden chambers. Eosinophil release from bone marrow was investigated in the in situ perfused guinea pig hind limb preparation. Respiratory burst and degranulation were measured by flow cytometry.

RESULTS

Cay10471 bound with high affinity to recombinant human and guinea pig CRTH2, but not DP, receptors. The antagonist prevented the PGD(2)-induced release of eosinophils from guinea pig bone marrow, and inhibited the chemotaxis of guinea pig bone marrow eosinophils and human peripheral blood eosinophils. Pretreatment with PGD(2) primed eosinophils for chemotaxis towards eotaxin, and this effect was prevented by Cay10471. In contrast, PGD(2) inhibited the C5a-induced up-regulation of CD63, a cellular marker of degranulation, in a Cay10471-sensitive manner. Finally, Cay10471 abolished the respiratory burst of eosinophils upon stimulation by PGD(2).

CONCLUSION

These data further emphasize the importance of CRTH2 in eosinophil function and show that Cay10471 is a highly potent and selective antagonist of PGD(2)-induced eosinophil responses. Cay10471 might hence be a useful compound for the treatment of allergic diseases.

摘要

背景

已发现Th2细胞上表达的趋化因子受体同源分子(CRTH2)是前列腺素(PG)D2的新型受体,PGD2是过敏反应期间肥大细胞释放的主要产物。本研究旨在分析新开发的CRTH2小分子拮抗剂Cay10471对嗜酸性粒细胞募集、呼吸爆发和脱颗粒功能的影响。

方法

使用微量博伊登小室测定豚鼠骨髓嗜酸性粒细胞和人外周血嗜酸性粒细胞的趋化性。在原位灌注的豚鼠后肢标本中研究骨髓中嗜酸性粒细胞的释放。通过流式细胞术测量呼吸爆发和脱颗粒。

结果

Cay10471与重组人及豚鼠CRTH2具有高亲和力结合,但不与DP受体结合。该拮抗剂可阻止PGD2诱导的豚鼠骨髓嗜酸性粒细胞释放,并抑制豚鼠骨髓嗜酸性粒细胞和人外周血嗜酸性粒细胞的趋化性。PGD2预处理可使嗜酸性粒细胞对嗜酸性粒细胞趋化因子产生趋化作用,而Cay10471可阻止这种作用。相反,PGD2以Cay10471敏感的方式抑制C5a诱导的脱颗粒细胞标志物CD63上调。最后,Cay10471消除了PGD2刺激后嗜酸性粒细胞的呼吸爆发。

结论

这些数据进一步强调了CRTH2在嗜酸性粒细胞功能中的重要性,并表明Cay10471是PGD2诱导的嗜酸性粒细胞反应的高效且选择性拮抗剂。因此,Cay10471可能是治疗过敏性疾病的有用化合物。

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