Interleukin-4 receptor signaling pathways in asthma pathogenesis

被引:167
作者
Chatila, TA [1 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Los Angeles, CA 90095 USA
关键词
D O I
10.1016/j.molmed.2004.08.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Asthma is a chronic allergic inflammatory disease, the initiation and progression of which is dependent on the cytokines interleukin (IL)-4 and IL-13 acting through related receptor complexes. Disease pathogenesis is effected by intracellular signaling pathways that couple primarily to specific motifs within the intracellular domain of the IL-4 receptor alpha chain (IL-4Ralpha), a subunit that is common to the IL-4 and IL-13 receptor complexes. Recent studies using genetic approaches have identified distinct functions for the respective IL-4Ralpha-coupled signaling pathways in regulating both early and chronic stages of asthma. Polymorphisms in components of the IL-4 and IL-13 cytokine-receptor axes are associated with allergy and asthma, suggesting that variations among individuals in the activity of this pathway contribute to disease susceptibility and manifestations.
引用
收藏
页码:493 / 499
页数:7
相关论文
共 74 条
[1]   Abrogation of bronchial eosinophilic inflammation and airway hyperreactivity in signal transducers and activators of transcription (STAT)6-deficient mice [J].
Akimoto, T ;
Numata, F ;
Tamura, M ;
Takata, Y ;
Higashida, N ;
Takashi, T ;
Takeda, K ;
Akira, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (09) :1537-1542
[2]   Analysis of the life cycle of Stat6 - Continuous cycling of Stat6 is required for IL-4 signaling [J].
Andrews, RP ;
Ericksen, MB ;
Cunningham, CM ;
Daines, MO ;
Hershey, GKK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (39) :36563-36569
[3]   Upregulation of IL-13 concentration in vivo by the IL13 variant associated with bronchial asthma [J].
Arima, K ;
Umeshita-Suyama, R ;
Sakata, Y ;
Akaiwa, M ;
Mao, XQ ;
Enomoto, T ;
Dake, Y ;
Shimazu, S ;
Yamashita, T ;
Sugawara, N ;
Brodeur, S ;
Geha, R ;
Puri, RK ;
Sayegh, MH ;
Adra, CN ;
Hamasaki, N ;
Hopkin, JM ;
Shirakawa, T ;
Izuhara, K .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2002, 109 (06) :980-987
[4]   IL-13-induced changes in the goblet cell density of human bronchial epithelial cell cultures: MAP kinase and phosphatidylinositol 3-kinase regulation [J].
Atherton, HC ;
Jones, G ;
Danahay, H .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2003, 285 (03) :L730-L739
[5]   Inhibition of inducible nitric oxide synthase expression by interleukin-4 and interleukin-13 in human lung epithelial cells [J].
Berkman, N ;
Robichaud, A ;
Robbins, RA ;
Roesems, G ;
Haddad, EB ;
Barnes, PJ ;
Chung, KF .
IMMUNOLOGY, 1996, 89 (03) :363-367
[6]   Targeted inactivation of the IL-4 receptor α chain 14R motif promotes allergic airway inflammation [J].
Blaeser, F ;
Bryce, PJ ;
Ho, N ;
Raman, V ;
Dedeoglu, F ;
Donaldson, DD ;
Geha, RS ;
Oettgen, HC ;
Chatila, TA .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (08) :1189-1200
[7]   Stat6-deficient mice develop airway hyperresponsiveness and peribronchial fibrosis during chronic fungal asthma [J].
Blease, K ;
Schuh, JM ;
Jakubzick, C ;
Lukacs, NW ;
Kunkel, SL ;
Joshi, BH ;
Puri, RK ;
Kaplan, MH ;
Hogaboam, CM .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 160 (02) :481-490
[8]   Janus kinase-dependent activation of insulin receptor substrate 1 in response to interleukin-4, oncostatin M, and the interferons [J].
Burfoot, MS ;
Rogers, NC ;
Watling, D ;
Smith, JM ;
Pons, S ;
Paonessaw, G ;
Pellegrini, S ;
White, MF ;
Kerr, IM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (39) :24183-24190
[9]   Advances in immunology - Asthma [J].
Busse, WW ;
Lemanske, RF .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (05) :350-362
[10]   Cell cooperation in development of eosinophil-predominant inflammation in airways [J].
Chaplin, DD .
IMMUNOLOGIC RESEARCH, 2002, 26 (1-3) :55-62