Electrophysiological properties of the airway - Epithelium in the murine, ovalbumin model of allergic airway disease

被引:6
作者
Cloutier, MM
Guernsey, L
Wu, CA
Thrall, RS
机构
[1] Univ Connecticut, Ctr Hlth, Dept Pediat, Farmington, CT USA
[2] Univ Connecticut, Ctr Hlth, Dept Med, Farmington, CT USA
关键词
D O I
10.1016/S0002-9440(10)63743-1
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The electrophysiological properties of cultured tracheal cells (CTCs) were examined in a murine (C57BL/6J), ovalbumin (OVA)-induced model of allergic airway disease (AAD) at early (3-day OVA-aerosol) and peak (10-day OVA-aerosol) periods of inflammation. Transepithelial potential difference, short-circuit current (Isc), and resistance (R-T) were lower in CTCs from 10-day OVA-aerosol animals compared to CTCs from naive mice. In cells cultured for 5 weeks, K, was greater in naive CTCs than in 10-day OVA-aerosol CTCs at all times (P < 0.01). The Isc response to mucosal amiloride (10(-4) mol/L) was increased in CTCs from 10-day OVA-aerosol mice compared to naive mice (6.0 +/- 0.37 muA/cm(2) versus 1.8 +/- 0.56 muA/cm(2); p < 0.001) with intermediate values for CTCs from 3-day OVA-aerosol mice. The cAMP-induced increase in Isc was blunted in 10-day OVA-aerosol animals compared to CTCs from naive mice (9 +/- 12% versus 39 +/- 7%; P < 0.01) with intermediate values for CTCs from 3-day OVA-aerosol mice. There was no difference in mannitol flux in naive compared to 10-day OVA-aerosol CTCs. Similar results were found using intact tracheas mounted in a perfusion chamber. These data demonstrate changes in airway epithelial cell function in the OVA-induced model of AAD that may contribute to the pathogenesis of airway inflammation.
引用
收藏
页码:1849 / 1856
页数:8
相关论文
共 35 条
[11]   Airway epithelium: more than just a barrier! [J].
Folkerts, G ;
Nijkamp, FP .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1998, 19 (08) :334-341
[12]   Ion transport across the normal and CF neonatal murine intestine [J].
Grubb, BR .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1999, 277 (01) :G167-G174
[13]   Epithelial-mesenchymal interactions in the pathogenesis of asthma [J].
Holgate, ST ;
Davies, DE ;
Lackie, PM ;
Wilson, SJ ;
Puddicombe, SM ;
Lordan, JL .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2000, 105 (02) :193-204
[14]  
Holgate Stephen T., 2003, Journal of Allergy and Clinical Immunology, V111, pS18, DOI 10.1067/mai.2003.25
[15]  
KNOWLES M, 1984, J APPL PHYSIOL, V56, P868, DOI 10.1152/jappl.1984.56.4.868
[16]   SIMPLE TECHNIQUE FOR CULTURE OF HIGHLY DIFFERENTIATED CELLS FROM DOG TRACHEAL EPITHELIUM [J].
KONDO, M ;
FINKBEINER, WE ;
WIDDICOMBE, JH .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (02) :L106-L117
[17]   Mycoplasma pulmonis inhibits electrogenic ion transport across murine tracheal epithelial cell monolayers [J].
Lambert, LC ;
Trummell, HQ ;
Singh, A ;
Cassell, GH ;
Bridges, RJ .
INFECTION AND IMMUNITY, 1998, 66 (01) :272-279
[18]   DIFFERENTIATED PROPERTIES OF RABBIT TRACHEAL EPITHELIAL-CELLS IN PRIMARY CULTURE [J].
LIEDTKE, CM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 255 (06) :C760-C770
[19]   Airway epithelium as an effector of inflammation: molecular regulation of secondary mediators [J].
Martin, LD ;
Rochelle, LG ;
Fischer, BM ;
Krunkosky, TM ;
Adler, KB .
EUROPEAN RESPIRATORY JOURNAL, 1997, 10 (09) :2139-2146
[20]   Coordinated clearance of periciliary liquid and mucus from airway surfaces [J].
Matsui, H ;
Randell, SH ;
Peretti, SW ;
Davis, CW ;
Boucher, RC .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (06) :1125-1131