Chronic hypoxia remodels voltage-gated Ca2+ entry in a human airway chemoreceptor cell line

被引:10
作者
Colebrooke, RL
Smith, IF
Kemp, PJ
Peers, C [1 ]
机构
[1] Univ Leeds, Cardiovasc Res Inst, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Leeds, Sch Biomed Sci, Leeds LS2 9JT, W Yorkshire, England
基金
英国惠康基金;
关键词
chemoreceptor; neuroepithelial body; H146; cell; chronic hypoxia; voltage-gated Ca2+ channel; microfluorimetry; Ca2+;
D O I
10.1016/S0304-3940(01)02479-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Arterial and airway chemoreceptors respond to acute hypoxia by depolarizing, thereby activating voltage-gated Ca2+ channels and so permitting Ca2+ entry to trigger transmitter release. Following periods of prolonged hypoxia, these cells undergo a form of remodelling which involves altered expression of ion channels. Here, we use microspectrofluorimetric recordings of voltage-gated Ca2+ entry (activated by exposure of cells to 50 mM K+) to show that chronic hypoxia suppresses such Ca2+ entry in model airway chemoreceptor (H146) cells. Furthermore, Ca2+ entry via L-type channels is suppressed, whilst entry via N-type channels is greatly enhanced. The suppressed response, together with dramatic remodelling of routes available for voltage-gated Ca2+ entry, is likely to alter significantly the acute O-2 sensing properties of these cells. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:69 / 72
页数:4
相关论文
共 20 条
[1]  
CODIGNOLA A, 1993, J BIOL CHEM, V268, P26240
[2]   Neuroepithelial bodies as airway oxygen sensors [J].
Cutz, E ;
Jackson, A .
RESPIRATION PHYSIOLOGY, 1999, 115 (02) :201-214
[3]  
DUCHEN MR, 1992, MONITORING NEURONAL, P231
[4]   CAROTID-BODY CHEMORECEPTORS - FROM NATURAL STIMULI TO SENSORY DISCHARGES [J].
GONZALEZ, C ;
ALMARAZ, L ;
OBESO, A ;
RIGUAL, R .
PHYSIOLOGICAL REVIEWS, 1994, 74 (04) :829-898
[5]   Amyloid β peptides mediate hypoxic augmentation of Ca2+ channels [J].
Green, KN ;
Peers, C .
JOURNAL OF NEUROCHEMISTRY, 2001, 77 (03) :953-956
[6]   O-2-sensing mechanisms in excitable cells: Role of plasma membrane K+ channels [J].
Haddad, GG ;
Jiang, C .
ANNUAL REVIEW OF PHYSIOLOGY, 1997, 59 :23-42
[7]   Combined antisense and pharmacological approaches implicate hTASK as an airway O2 sensing K+ channel [J].
Hartness, ME ;
Lewis, A ;
Searle, GJ ;
O'Kelly, I ;
Peers, C ;
Kemp, PJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (28) :26499-26508
[8]   Cellular mechanisms of oxygen sensing [J].
López-Barneo, J ;
Pardal, R ;
Ortega-Sáenz, P .
ANNUAL REVIEW OF PHYSIOLOGY, 2001, 63 :259-287
[9]   O2-sensitive K+ channels in neuroepithelial body-derived small cell carcinoma cells of the human lung [J].
O'Kelly, I ;
Peers, C ;
Kemp, PJ .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1998, 275 (04) :L709-L716
[10]   Potential identification of the O2-sensitive K+ current in a human neuroepithelial body-derived cell line [J].
O'Kelly, I ;
Stephens, RH ;
Peers, C ;
Kemp, PJ .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1999, 276 (01) :L96-L104