Lipopolysaccharide hyperpolarizes guinea pig airway epithelium by increasing the activities of the epithelial Na+ channel and the Na+-K+ pump

被引:9
作者
Dodrill, Michael W.
Fedan, Jeffrey S.
机构
[1] W Virginia Univ, Sch Pharm, Robert C Byrd Hlth Sci Ctr, Dept Basic Pharmaceut Sci, Morgantown, WV 26506 USA
[2] NIOSH, Hlth Effects Lab Div, Morgantown, WV USA
关键词
endotoxin; lung; airway epithelium; Na+ transport; transepithelial voltage; ALVEOLAR EPITHELIUM; CELL MONOLAYERS; TNF-ALPHA; TRANSPORT; EXPRESSION; ATPASE; ION; CLEARANCE; HYPOXIA;
D O I
10.1152/ajplung.00123.2010
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Dodrill MW, Fedan JS. Lipopolysaccharide hyperpolarizes guinea pig airway epithelium by increasing the activities of the epithelial Na+ channel and the Na+-K+ pump. Am J Physiol Lung Cell Mol Physiol 299: L550-L558, 2010. First published July 16, 2010; doi:10.1152/ajplung.00123.2010.-Earlier, we found that systemic administration of lipopolysaccharide (LPS; 4 mg/kg) hyperpolarized the transepithelial potential difference (V-t) of tracheal epithelium in the isolated, perfused trachea (IPT) of the guinea pig 18 h after injection. As well, LPS increased the hyperpolarization component of the response to basolateral methacholine, and potentiated the epithelium-derived relaxing factor-mediated relaxation responses to hyperosmolar solutions applied to the apical membrane. We hypothesized that LPS stimulates the transepithelial movement of Na+ via the epithelial sodium channel (ENaC)/Na+-K+ pump axis, leading to hyperpolarization of V-t. LPS increased the V-t-depolarizing response to amiloride (10 mu M), i.e., offset the effect of LPS, indicating that Na+ transport activity was increased. The functional activity of ENaC was measured in the IPT after short-circuiting the Na+-K+ pump with basolateral amphotericin B (7.5 mu M). LPS had no effect on the hyperpolarization response to apical trypsin (100 U/ml) in the Ussing chamber, indicating that channel-activating proteases are not involved in the LPS-induced activation of ENaC. To assess Na+-K+ pump activity in the IPT, ENaC was short-circuited with apical amphotericin B. The greater Vt in the presence of amphotericin B in tracheas from LPS-treated animals compared with controls revealed that LPS increased Na+-K+ pump activity. This finding was confirmed in the Ussing chamber by inhibiting the Na+-K+ pump via extracellular K+ removal, loading the epithelium with Na+, and observing a greater hyperpolarization response to K+ restoration. Together, the findings of this study reveal that LPS hyperpolarizes the airway epithelium by increasing the activities of ENaC and the Na+-K+ pump.
引用
收藏
页码:L550 / L558
页数:9
相关论文
共 21 条
[1]   Augmentation of endogenous dopamine production increases lung liquid clearance [J].
Adir, Y ;
Azzam, ZS ;
Lecuona, E ;
Leal, S ;
Pesce, L ;
Dumasius, V ;
Bertorello, AM ;
Factor, P ;
Young, JB ;
Ridge, KM ;
Sznajder, JI .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2004, 169 (06) :757-763
[2]   Dexamethasone upregulates the Na-K-ATPase in rat alveolar epithelial cells [J].
Barquin, N ;
Ciccolella, DE ;
Ridge, KM ;
Sznajder, JI .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1997, 273 (04) :L825-L830
[3]   Na+ transport in normal and CF human bronchial epithelial cells is inhibited by BAY 39-9437 [J].
Bridges, RJ ;
Newton, BB ;
Pilewski, JM ;
Devor, DC ;
Poll, CT ;
Hall, RL .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2001, 281 (01) :L16-L23
[4]   Downregulation of ENaC activity and expression by TNF-α in alveolar epithelial cells [J].
Dagenais, A ;
Fréchette, R ;
Yamagata, Y ;
Yamagata, T ;
Carmel, JF ;
Clermont, ME ;
Brochiero, E ;
Massé, C ;
Berthiaume, Y .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2004, 286 (02) :L301-L311
[5]  
DORTCHCARNES J, 2001, AM J PHYSIOL-LUNG C, V281, pL450
[6]   Mechanisms of TNF-α stimulation of amiloride-sensitive sodium transport across alveolar epithelium [J].
Fukuda, N ;
Jayr, C ;
Lazrak, A ;
Wang, YB ;
Lucas, R ;
Matalon, S ;
Matthay, MA .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2001, 280 (06) :L1258-L1265
[7]   FXYD proteins: new regulators of Na-k-ATPase [J].
Geering, K .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2006, 290 (02) :F241-F250
[8]   ELECTROGENIC SODIUM-PUMP IN ARTERIAL SMOOTH-MUSCLE CELLS [J].
HENDRICKX, H ;
CASTEELS, R .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1974, 346 (04) :299-306
[9]   Decreased expression of both the α1- and α2-subunits of the Na-K-ATPase reduces maximal alveolar epithelial fluid clearance [J].
Looney, MR ;
Sartori, C ;
Chakraborty, S ;
James, PF ;
Lingrel, JB ;
Matthay, MA .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2005, 289 (01) :L104-L110
[10]   Alveolar epithelial ion and fluid transport -: Hypoxia decreases active Na transport across primary rat alveolar epithelial cell monolayers [J].
Mairbäurl, H ;
Mayer, K ;
Kim, KJ ;
Borok, Z ;
Bärtsch, P ;
Crandall, ED .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2002, 282 (04) :L659-L665