Fundamental signals that regulate eosinophil homing to the gastrointestinal tract

被引:305
作者
Mishra, A
Hogan, SP
Lee, JJ
Foster, PS
Rothenberg, ME
机构
[1] Childrens Hosp, Med Ctr, Dept Pediat, Div Pulm Med Allergy & Clin Immunol, Cincinnati, OH 45229 USA
[2] Mayo Clin Scottsdale, Dept Biochem & Mol Biol, Scottsdale, AZ 85259 USA
[3] Australian Natl Univ, John Curtin Sch Med, Canberra, ACT 0200, Australia
关键词
D O I
10.1172/JCI6560
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The histological identification of increased eosinophils in the gastrointestinal tract occurs in numerous clinical disorders; however, there is a limited understanding of the mechanisms regulating eosinophil trafficking into this mucosal surface. The results presented in this study characterize the processes regulating eosinophil homing into the gastrointestinal tract at baseline. Eosinophils were found to be present in the lamina propria of 19-day-old embryos and germ-free adult mice at concentrations comparable to those present in non-germ-free adult mice. Furthermore, eosinophil gastrointestinal levels were not altered by increasing circulating eosinophils after pulmonary allergen challenge. Gastrointestinal eosinophil levels were partially reduced in mice deficient in recombinase activating gene-1 (RAG-1), IL-5, or the beta common chain (beta c), but these reductions paralleled reductions in circulating eosinophils. In contrast, mice deficient in eotaxin had a marked reduction in gastrointestinal eosinophils but normal levels of eosinophils in the hematopoietic compartments. Furthermore, eotaxin was important for regulating eosinophil levels, even in the presence of high levels of IL-5. These investigations demonstrate eosinophil homing into the gastrointestinal tract during embryonic development occurring independently of viable intestinal flora. Furthermore, eotaxin is identified as the primary regulator of eosinophil gastrointestinal: homing under homeostatic states, and may therefore have a fundamental role in innate immune responses.
引用
收藏
页码:1719 / 1727
页数:9
相关论文
共 57 条
[1]   ADHESION TO FIBRONECTIN PROLONGS EOSINOPHIL SURVIVAL [J].
ANWAR, ARF ;
MOQBEL, R ;
WALSH, GM ;
KAY, AB ;
WARDLAW, AJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (03) :839-843
[2]  
BAGGIOLINI M, 1994, ADV IMMUNOL, V55, P97
[3]  
Bartels Joachim, 1997, Rhinology (Utrecht), V35, P171
[4]   ALPHA-4-BETA-7-INTEGRIN MEDIATES LYMPHOCYTE BINDING TO THE MUCOSAL VASCULAR ADDRESSIN MADCAM-1 [J].
BERLIN, C ;
BERG, EL ;
BRISKIN, MJ ;
ANDREW, DP ;
KILSHAW, PJ ;
HOLZMANN, B ;
WEISSMAN, IL ;
HAMANN, A ;
BUTCHER, EC .
CELL, 1993, 74 (01) :185-195
[5]   THE ROLE OF ADHESION MOLECULES IN HUMAN EOSINOPHIL AND BASOPHIL RECRUITMENT [J].
BOCHNER, BS ;
SCHLEIMER, RP .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1994, 94 (03) :427-438
[6]  
Brown JR, 1998, CLIN EXP IMMUNOL, V114, P137
[7]   COOPERATION BETWEEN INTERLEUKIN-5 AND THE CHEMOKINE EOTAXIN TO INDUCE EOSINOPHIL ACCUMULATION IN-VIVO [J].
COLLINS, PD ;
MARLEAU, S ;
GRIFFITHSJOHNSON, DA ;
JOSE, PJ ;
WILLIAMS, TJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (04) :1169-1174
[8]   CLONING AND FUNCTIONAL EXPRESSION OF A HUMAN EOSINOPHIL CC-CHEMOKINE RECEPTOR [J].
COMBADIERE, C ;
AHUJA, SK ;
MURPHY, PM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (28) :16491-16494
[9]   REQUIREMENT OF MIP-1-ALPHA FOR AN INFLAMMATORY RESPONSE TO VIRAL-INFECTION [J].
COOK, DN ;
BECK, MA ;
COFFMAN, TM ;
KIRBY, SL ;
SHERIDAN, JF ;
PRAGNELL, IB ;
SMITHIES, O .
SCIENCE, 1995, 269 (5230) :1583-1585
[10]   Cloning, expression, and characterization of the human eosinophil eotaxin receptor [J].
Daugherty, BL ;
Siciliano, SJ ;
DeMartino, JA ;
Malkowitz, L ;
Sirotina, A ;
Springer, MS .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (05) :2349-2354