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

被引:45
作者
Royer, J. F.
Schratl, P.
Lorenz, S.
Kostenis, E.
Ulven, T.
Schuligoi, R.
Peskar, B. A.
Heinemann, A.
机构
[1] Med Univ Graz, Inst Expt & Clin Pharmacol, A-8010 Graz, Austria
[2] Inst Pharmaceut Biol, Bonn, Germany
[3] Univ So Denmark, Dept Chem & Phys, Odense M, Denmark
基金
奥地利科学基金会;
关键词
allergy; bone marrow; chemoattractant receptor-homologous molecule expressed on Th2 cells; chemotaxis; D-type prostanoid receptor; eosinophils; prostaglandins;
D O I
10.1111/j.1398-9995.2007.01452.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:1401 / 1409
页数:9
相关论文
共 24 条
[1]   Effects of prostaglandin D2, 15-deoxy-Δ12,14-prostaglandin J2, and selective DP1 and DP2 receptor agonists on pulmonary infiltration of eosinophils in Brown Norway rats [J].
Almishri, W ;
Cossette, C ;
Rokach, J ;
Martin, JG ;
Hamid, Q ;
Powell, WS .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2005, 313 (01) :64-69
[2]   11-dehydro-thromboxane B2, a stable thromboxane metabolite, is a full agonist of chemoattractant receptor-homologous molecule expressed on TH2 cells (CRTH2) in human eosinophils and basophils [J].
Böhm, E ;
Sturm, GJ ;
Weiglhofer, I ;
Sandig, H ;
Shichijo, M ;
McNamee, A ;
Pease, JE ;
Kollroser, M ;
Peskar, BA ;
Heinemann, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (09) :7663-7670
[3]   Pronounced eosinophilic lung inflammation and Th2 cytokine release in human lipocalin-type prostaglandin D synthase transgenic mice [J].
Fujitani, Y ;
Kanaoka, Y ;
Aritake, K ;
Uodome, N ;
Okazaki-Hatake, K ;
Urade, Y .
JOURNAL OF IMMUNOLOGY, 2002, 168 (01) :443-449
[4]   Asthma exacerbations and sputum eosinophil counts: a randomised controlled trial [J].
Green, RH ;
Brightling, CE ;
McKenna, S ;
Hargadon, B ;
Parker, D ;
Bradding, P ;
Wardlaw, AJ ;
Pavord, ID .
LANCET, 2002, 360 (9347) :1715-1721
[5]   THE ROLE OF PROSTANOID TP-RECEPTOR AND DP-RECEPTOR IN THE BRONCHOCONSTRICTOR EFFECT OF INHALED PGD2 IN ANESTHETIZED GUINEA-PIGS - EFFECT OF THE DP-ANTAGONIST BW-A868C [J].
HAMIDBLOOMFIELD, S ;
PAYNE, AN ;
PETROVIC, AA ;
WHITTLE, BJR .
BRITISH JOURNAL OF PHARMACOLOGY, 1990, 100 (04) :761-766
[6]   Identification of selective basophil chemoattractants in human nasal polyps as insulin-like growth factor-1 and insulin-like growth factor-2 [J].
Hartnell, A ;
Heinemann, A ;
Conroy, DM ;
Wait, R ;
Sturm, GJ ;
Caversaccio, M ;
Jose, PJ ;
Williams, TJ .
JOURNAL OF IMMUNOLOGY, 2004, 173 (10) :6448-6457
[7]   Δ12-Prostaglandin J2, a plasma causes eosinophil mobilization metabolite of prostaglandin D2, from the bone marrow and primes eosinophils for chemotaxis [J].
Heinemann, A ;
Schuligoi, R ;
Sabroe, I ;
Hartnell, A ;
Peskar, BA .
JOURNAL OF IMMUNOLOGY, 2003, 170 (09) :4752-4758
[8]   Prostaglandin D2 selectively induces chemotaxis in T helper type 2 cells, eosinophils, and basophils via seven-transmembrane receptor CRTH2 [J].
Hirai, H ;
Tanaka, K ;
Yoshie, O ;
Ogawa, K ;
Kenmotsu, K ;
Takamori, Y ;
Ichimasa, M ;
Sugamura, K ;
Nakamura, M ;
Takano, S ;
Nagata, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 193 (02) :255-261
[9]   A critical role for eosinophils in allergic airways remodeling [J].
Humbles, AA ;
Lloyd, CM ;
McMillan, SJ ;
Friend, DS ;
Xanthou, G ;
McKenna, EE ;
Ghiran, S ;
Gerard, NP ;
Yu, CN ;
Orkin, SH ;
Gerard, C .
SCIENCE, 2004, 305 (5691) :1776-1779
[10]   A highly conserved glycine within linker I and the extreme C terminus of G protein α subunits interact cooperatively in switching G protein-coupled receptor-to-effector specificity [J].
Kostenis, E ;
Martini, L ;
Ellis, J ;
Waldhoer, M ;
Heydorn, A ;
Rosenkilde, MM ;
Norregaard, PK ;
Jorgensen, R ;
Whistler, JL ;
Milligan, G .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2005, 313 (01) :78-87