Regulation of IL-5 receptor on eosinophil progenitors in allergic inflammation: Role of retinoic acid

被引:22
作者
Denburg, JA [1 ]
Sehmi, R [1 ]
Upham, J [1 ]
机构
[1] McMaster Univ, Dept Med, Hamilton, ON L8N 3Z5, Canada
关键词
IL-5; receptor; retinoic acid; eosinophils; asthma; hemopoiesis;
D O I
10.1159/000053724
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
We and others have shown that IL-5 plays a central role in eosinophil and basophil differentiation, exerting its effects through the IL-5 receptor (IL-5R). Little is currently known concerning regulation of IL-5R alpha gene transcription in the context of commitment of hemopoietic progenitor cells to the eosinophil and basophil lineages; recent studies have indicated that IL-5 itself can regulate IL-5R alpha expression on mature eosinophils. We now provide evidence to indicate that IL-5 can upregulate IL-5R alpha. on bone marrow CD34+ progenitors in vitro, as we have demonstrated in vivo in atopic asthmatics. Given that all-trans retinoic acid (ATRA) is known to modulate some granulopoiesis, causing neutrophilic differentiation, we examined the effects of ATRA on eosinophil/basophil differentiation and IL-5R alpha expression. In cultures of normal human bone marrow, ATRA selectively suppressed eosinophil/basophil differentiation. Similarly, ATRA inhibited eosinophil/basophil differentiation of cord blood CD34+ cells, while neutrophil differentiation proceeded without impediment. Most importantly, these effects of ATRA on CD34+ cells were associated with selective, dose-dependent inhibition of membrane-bound IL-5Ra, upregulation of soluble IL-5R alpha transcription, but no change in GM-CSF receptor expression. These findings indicate that retinoids can differentially regulate membrane and soluble isoforms of IL-5R alpha, and that these effects have functional consequences in vitro on eosinophil and basophil differentiation. ATRA may be of therapeutic benefit in allergic inflammatory disorders in which eosinophil differentiation and membrane-bound IL-5R are upregulated. Copyright (C) 2001 S. Karger AG, Basel.
引用
收藏
页码:246 / 248
页数:3
相关论文
共 7 条
[1]   INTERLEUKIN-5 AND ITS RECEPTOR - A DRUG TARGET FOR EOSINOPHILIA ASSOCIATED WITH CHRONIC ALLERGIC DISEASE [J].
DEVOS, R ;
PLAETINCK, G ;
CORNELIS, S ;
GUISEZ, Y ;
VANDERHEYDEN, J ;
TAVERNIER, J .
JOURNAL OF LEUKOCYTE BIOLOGY, 1995, 57 (06) :813-819
[2]  
GRATAS C, 1993, LEUKEMIA, V7, P1156
[3]   Retinoic acid is a negative regulator for the differentiation of cord blood-derived human mast cell progenitors [J].
Kinoshita, T ;
Koike, K ;
Mwamtemi, HH ;
Ito, S ;
Ishida, S ;
Nakazawa, Y ;
Kurokawa, Y ;
Sakashita, K ;
Higuchi, T ;
Takeuchi, K ;
Sawai, N ;
Shiohara, M ;
Kamijo, T ;
Kawa, S ;
Yamashita, T ;
Komiyama, A .
BLOOD, 2000, 95 (09) :2821-2828
[4]   CHANGING THE DIFFERENTIATION PROGRAM OF HEMATOPOIETIC-CELLS - RETINOIC ACID-INDUCED SHIFT OF EOSINOPHIL-COMMITTED CELLS TO NEUTROPHILS [J].
PAUL, CC ;
MAHRER, S ;
TOLBERT, M ;
ELBERT, BL ;
WONG, I ;
ACKERMAN, SJ ;
BAUMANN, MA .
BLOOD, 1995, 86 (10) :3737-3744
[5]   MODULATION OF GROWTH AND DIFFERENTIATION OF EOSINOPHILS FROM HUMAN PERIPHERAL-BLOOD CD34(+) CELLS BY IL5 AND OTHER GROWTH-FACTORS [J].
SHALIT, M ;
SEKHSARIA, S ;
MALECH, HL .
CELLULAR IMMUNOLOGY, 1995, 160 (01) :50-57
[6]   Interleukin 5 regulates the isoform expression of its own receptor α-subunit [J].
Tavernier, J ;
Van der Heyden, J ;
Verhee, A ;
Brusselle, G ;
Van Ostade, X ;
Vandekerckhove, J ;
North, J ;
Rankin, SM ;
Kay, AB ;
Robinson, DS .
BLOOD, 2000, 95 (05) :1600-1607
[7]  
ZANDERS ED, 1994, EUR CYTOKINE NETW, V5, P35