Effects of in vitro exposure to hay dust on the gene expression of chemokines and cell-surface receptors in primary bronchial epithelial cell cultures established from horses with chronic recurrent airway obstruction

被引:17
作者
Ainsworth, Dorothy M. [1 ]
Matychak, MaryBeth [1 ]
Reyner, Claudia L. [3 ]
Erb, Hollis N. [2 ]
Young, Jean C. [1 ]
机构
[1] Cornell Univ, Coll Vet Med, Dept Clin Sci, Ithaca, NY 14853 USA
[2] Cornell Univ, Coll Vet Med, Dept Populat Med & Diagnost Sci, Ithaca, NY 14853 USA
[3] Cornell Univ, Coll Agr & Life Sci, Dept Anim Sci, Ithaca, NY 14853 USA
关键词
BRONCHOALVEOLAR LAVAGE CELLS; TOLL-LIKE RECEPTORS; PULMONARY-DISEASE; MESSENGER-RNA; LUNG-DISEASE; IFN-GAMMA; INFLAMMATION; ASTHMA; INTERLEUKIN-1-BETA; NEUTROPHIL;
D O I
10.2460/ajvr.70.3.365
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Objective-To examine effects of in vitro exposure to solutions of hay dust, lipopolysaccharide (LPS), or beta-glucan on chemokine and cell-surface receptor (CSR) gene expression in primary bronchial epithelial cell cultures (BECCs) established from healthy horses and horses with recurrent airway obstruction (RAO). Sample Population-BECCs established from bronchial biopsy specimens of 6 RAO-affected horses and 6 healthy horses. Procedures-5-day-old BECCs were treated with PBS solution, hay dust solutions, LPS, or P-glucan for 6 or 24 hours. Gene expression of interleukin (IL)-8, chemokine (C-X-C motif) ligand 2 (CXCL2), IL-1 beta, toll-like receptor 2, toll-like receptor 4, IL-1 receptor 1, and glyceraldehyde 3-phosphate dehydrogenase was measured with a kinetic PCR assay. Results-Treatment with PBS solution for 6 or 24 hours was not associated with a significant difference in chemokine or CSR expression between BECCs from either group of horses. In all BECCs, treatment with hay dust or LPS for 6 hours increased IL-8, CXCL2, and IL-1 beta gene expression -> 3-fold; at 24 hours, only IL-1 beta expression was upregulated by > 3-fold. In all BECCs, CSR gene expression was not increased following any treatment. With the exception of a 3.7-fold upregulation of CXCL2 in BECCs from RAO-affected horses (following 6-hour hay dust treatment), no differences in chemokine or CSR gene expression were detected between the 2 groups. At 24 hours, CXCL2 gene expression in all BECCs was downregulated. Conclusions and Clinical Relevance-Epithelial CXCL2 upregulation in response to hay dust particulates may incite early airway neutrophilia in horses with RAO. (Am J Vet Res 2009;70:365-372)
引用
收藏
页码:365 / 372
页数:8
相关论文
共 39 条
[11]   Cytokines as targets in chronic obstructive pulmonary disease [J].
Chung, K. F. .
CURRENT DRUG TARGETS, 2006, 7 (06) :675-681
[12]  
Couëtil LL, 2006, J VET INTERN MED, V20, P399, DOI 10.1892/0891-6640(2006)20[399:EOBDAD]2.0.CO
[13]  
2
[14]   The effect of adding oral dexamethasone to feed alterations on the airway cell inflammatory gene expression in stabled horses affected with recurrent airway obstruction [J].
DeLuca, L. ;
Erb, H. N. ;
Young, J. C. ;
Perkins, G. A. ;
Ainsworth, D. M. .
JOURNAL OF VETERINARY INTERNAL MEDICINE, 2008, 22 (02) :427-435
[15]   EARLY NEUTROPHIL BUT NOT EOSINOPHIL OR PLATELET RECRUITMENT TO THE LUNGS OF ALLERGIC HORSES FOLLOWING ANTIGEN EXPOSURE [J].
FAIRBAIRN, SM ;
PAGE, CP ;
LEES, P ;
CUNNINGHAM, FM .
CLINICAL AND EXPERIMENTAL ALLERGY, 1993, 23 (10) :821-828
[16]   Chemokines in bronchiolar epithelium in the development of chronic obstructive pulmonary disease [J].
Fuke, S ;
Betsuyaku, T ;
Nasuhara, Y ;
Morikawa, T ;
Katoh, H ;
Nishimura, M .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2004, 31 (04) :405-412
[17]   Pulmonary chemokine expression is coordinately regulated by STAT1, STAT6, and IFN-γ [J].
Fulkerson, PC ;
Zimmermann, N ;
Hassman, LM ;
Finkelman, FD ;
Rothenberg, ME .
JOURNAL OF IMMUNOLOGY, 2004, 173 (12) :7565-7574
[18]   The role of the epidermal growth factor receptor in sustaining neutrophil inflammation in severe asthma [J].
Hamilton, LM ;
Torres-Lozano, C ;
Puddicombe, SM ;
Richter, A ;
Kimber, I ;
Dearman, RJ ;
Vrugt, B ;
Aalbers, R ;
Holgate, ST ;
Djukanovic, R ;
Wilson, SJ ;
Davies, DE .
CLINICAL AND EXPERIMENTAL ALLERGY, 2003, 33 (02) :233-240
[19]   Innate immune responses to environmental allergens [J].
Kauffman, HF .
CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY, 2006, 30 (02) :129-140
[20]   The role of chemokines in neutrophil biology [J].
Kobayashi, Yoshiro .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2008, 13 :2400-2407