Interleukin 9: A candidate gene for asthma

被引:187
作者
Nicolaides, NC
Holroyd, KJ
Ewart, SL
Eleff, SM
Kiser, MB
Dragwa, CR
Sullivan, CD
Grasso, L
Zhang, LY
Messler, CJ
Zhou, TY
Kleeberger, SR
Buetow, KH
Levitt, RC
机构
[1] MAGAININ PHARMACEUT, MAGAININ INST MOL MED, PLYMOUTH MEETING, PA 19462 USA
[2] MICHIGAN STATE UNIV, CTR VET MED, E LANSING, MI 48824 USA
[3] JOHNS HOPKINS MED INST, DEPT ANESTHESIOL & CRIT CARE MED, BALTIMORE, MD 21287 USA
[4] JOHNS HOPKINS MED INST, DEPT ENVIRONM HLTH SCI, BALTIMORE, MD 21287 USA
[5] FOX CHASE CANC CTR, DIV POPULAT SCI, PHILADELPHIA, PA 19111 USA
关键词
D O I
10.1073/pnas.94.24.13175
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Asthma is a complex heritable inflammatory disorder of the airways associated with clinical signs of atopy and bronchial hyperresponsiveness. Recent studies localized a major gene for asthma to chromosome 5q31-q33 in humans. Thus, this segment of the genome represents a candidate region for genes that determine susceptibility to bronchial hyperresponsiveness and atopy in animal models. Homologs of candidate genes on human chromosome 5q31-q33 are found in four regions in the mouse genome, two on chromosome 18, and one each on chromosomes 11 and 13. We assessed bronchial responsiveness as a quantitative trait in mice and found it linked to chromosome 13. Interleukin 9 (IL-9) is located in the linked region and was analyzed as a gene candidate. The expression of IL-9 was markedly reduced in bronchial hyporesponsive mice, and the level of expression was determined by sequences within the qualitative trait locus (QTL). These data suggest a role for IL-9 in the complex pathogenesis of bronchial hyperresponsiveness as a risk factor for asthma.
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页码:13175 / 13180
页数:6
相关论文
共 33 条
[1]  
CHURCHILL GA, 1994, GENETICS, V138, P963
[2]   Human/mouse homology relationships [J].
DeBry, RW ;
Seldin, MF .
GENOMICS, 1996, 33 (03) :337-351
[3]   ALLERGEN EXPOSURE INDUCES THE ACTIVATION OF ALLERGEN-SPECIFIC TH2 CELLS IN THE AIRWAY MUCOSA OF PATIENTS WITH ALLERGIC RESPIRATORY DISORDERS [J].
DELPRETE, GF ;
DECARLI, M ;
DELIOS, MM ;
MAESTRELLI, P ;
RICCI, M ;
FABBRI, L ;
ROMAGNANI, S .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (07) :1445-1449
[4]   T-lymphocytes regulate genetically determined airway hyperresponsiveness in mice [J].
DeSanctis, GT ;
Itoh, A ;
Green, FHY ;
Qin, SX ;
Kimura, T ;
Grobholz, JK ;
Martin, TR ;
Maki, T ;
Drazen, JM .
NATURE MEDICINE, 1997, 3 (04) :460-462
[5]  
DIETRICH W, 1992, GENETICS, V131, P423
[6]   Allelic association of gene markers on chromosomes 5q and 11q with atopy and bronchial hyperresponsiveness [J].
Doull, IJM ;
Lawrence, S ;
Watson, M ;
Begishvili, T ;
Beasley, RW ;
Lampe, F ;
Holgate, ST ;
Morton, NE .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 153 (04) :1280-1284
[7]   INTERLEUKIN-9 POTENTIATES THE INTERLEUKIN-4-INDUCED IMMUNOGLOBULIN (IGG, IGM AND IGE) PRODUCTION BY NORMAL HUMAN B-LYMPHOCYTES [J].
DUGAS, B ;
RENAULD, JC ;
PENE, J ;
BONNEFOY, JY ;
PETIFRERE, C ;
BRAQUET, P ;
BOUSQUET, J ;
VANSNICK, J ;
MENCIAHUERTA, JM .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (07) :1687-1692
[8]  
EKLUND KK, 1993, J IMMUNOL, V151, P4266
[9]   RESPIRATORY SYSTEM MECHANICS IN MICE MEASURED BY END-INFLATION OCCLUSION [J].
EWART, S ;
LEVITT, R ;
MITZNER, W .
JOURNAL OF APPLIED PHYSIOLOGY, 1995, 79 (02) :560-566
[10]   DIFFERENTIAL REGULATION OF IL-9-EXPRESSION AFTER INFECTION WITH LEISHMANIA-MAJOR IN SUSCEPTIBLE AND RESISTANT MICE [J].
GESSNER, A ;
BLUM, H ;
ROLLINGHOFF, M .
IMMUNOBIOLOGY, 1993, 189 (05) :419-435