Expression of IL-4/IL-13 receptors in differentiating human airway epithelial cells

被引:25
作者
White, Steven R. [1 ]
Martin, Linda D. [2 ]
Stern, Randi [1 ]
Laxman, Bharathi [1 ]
Marroquin, Bertha A. [1 ]
机构
[1] Univ Chicago, Sect Pulm & Crit Care Med, Dept Med, Chicago, IL 60637 USA
[2] N Carolina State Univ, Dept Chem, Raleigh, NC 27695 USA
关键词
interleukin-4; interleukin-13; eotaxin-3; migration; BRONCHIAL BIOPSY SPECIMENS; NF-KAPPA-B; SIGNAL-TRANSDUCTION; IL-4; RECEPTOR; INSULIN-RECEPTOR; IN-VITRO; INTERLEUKIN-4; GENE-EXPRESSION; ATOPIC ASTHMA; GAMMA-CHAIN;
D O I
10.1152/ajplung.00422.2009
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
White SR, Martin LD, Stern R, Laxman B, Marroquin BA. Expression of IL-4/IL-13 receptors in differentiating human airway epithelial cells. Am J Physiol Lung Cell Mol Physiol 299: L681-L693, 2010. First published August 20, 2010; doi:10.1152/ajplung.00422.2009.-IL-4 and IL-13 elicit several important responses in airway epithelium including chemokine secretion and mucous secretion that may contribute to airway inflammation, cell migration, and differentiation. These cytokines have overlapping but not identical effector profiles likely due to shared subunits in their receptor complexes. These receptors are variably described in epithelial cells, and the relative expression, localization, and function of these receptors in differentiated and repairing epithelial cells are not clear. We examined IL-4/IL-13 receptor expression and localization in primary airway epithelial cells collected from normal human lungs and grown under conditions yielding both undifferentiated and differentiated cells inclusive of basal, goblet, and ciliated cell phenotypes. Gene expression of the IL-4R alpha, IL-2R gamma c, IL-13R alpha 1, and IL-13R alpha 2 receptor subunits increased with differentiation, but different patterns of localization and protein abundance were seen for each subunit based on both differentiation and the cell subtypes present. Increased expression of receptor subunits observed in more differentiated cells was associated with more substantial functional responses to IL-4 stimulation including increased eotaxin-3 expression and accelerated migration after injury. We demonstrate substantial differences in IL-4/IL-13 receptor subunit expression and responsiveness to IL-4 based on the extent of airway epithelial cell differentiation and suggest that these differences may have functional consequences in airway inflammation.
引用
收藏
页码:L681 / L693
页数:13
相关论文
共 67 条
[31]   AIRWAY MUCOSAL INFLAMMATION EVEN IN PATIENTS WITH NEWLY DIAGNOSED ASTHMA [J].
LAITINEN, LA ;
LAITINEN, A ;
HAAHTELA, T .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1993, 147 (03) :697-704
[32]   DAMAGE OF THE AIRWAY EPITHELIUM AND BRONCHIAL REACTIVITY IN PATIENTS WITH ASTHMA [J].
LAITINEN, LA ;
HEINO, M ;
LAITINEN, A ;
KAVA, T ;
HAAHTELA, T .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1985, 131 (04) :599-606
[33]  
Lankford SM, 2005, IN VITRO CELL DEV-AN, V41, P217
[34]  
LEONARD WJ, 1994, ADV EXP MED BIOL, V365, P225
[35]   Mucins as differentiation markers in bronchial epithelium -: Squamous cell carcinoma and adenocarcinoma display similar expression patterns [J].
López-Ferrer, A ;
Curull, V ;
Barranco, C ;
Garrido, M ;
Lloreta, J ;
Real, FX ;
de Bolós, C .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2001, 24 (01) :22-29
[36]   Cooperative effects of Th2 cytokines and allergen on normal and asthmatic bronchial epithelial cells [J].
Lordan, JL ;
Bucchieri, F ;
Richter, A ;
Konstantinidis, A ;
Holloway, JW ;
Thornber, M ;
Puddicombe, SM ;
Buchanan, D ;
Wilson, SJ ;
Djukanovic, R ;
Holgate, ST ;
Davies, DE .
JOURNAL OF IMMUNOLOGY, 2002, 169 (01) :407-414
[37]  
Matsukura S, 1999, J IMMUNOL, V163, P6876
[38]   Alcohol Primes the Airway for Increased Interleukin-13 Signaling [J].
Mitchell, Patrick O. ;
Jensen, J. Spencer ;
Ritzenthaler, Jeffrey D. ;
Roman, Jesse ;
Pelaez, Andres ;
Guidot, David M. .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2009, 33 (03) :505-513
[39]  
MONTEFORT S, 1992, THORAX, V47, pP232
[40]  
Morishima Y, 2001, AM J RESP CELL MOL, V24, P1