DEG/ENaC ion channels involved in sensory transduction are modulated by cold temperature

被引:139
作者
Askwith, CC
Benson, CJ
Welsh, MJ
Snyder, PM
机构
[1] Univ Iowa, Coll Med, Dept Internal Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Coll Med, Dept Physiol & Biophys, Iowa City, IA 52242 USA
[3] Univ Iowa, Coll Med, Howard Hughes Med Inst, Iowa City, IA 52242 USA
关键词
D O I
10.1073/pnas.111155398
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Several DEG/ENaC cation channel subunits are expressed in the tongue and in cutaneous sensory neurons, where they are postulated to function as receptors for salt and sour taste and for touch. Because these tissues are exposed to large temperature variations, we examined how temperature affects DEG/ENaC channel function. We found that cold temperature markedly increased the constitutively active Na+ currents generated by epithelial Na+ channels (ENaC), Half-maximal stimulation occurred at 25 degreesC. Cold temperature did not induce current from other DEG/ENaC family members (BNC1, ASIC, and DRASIC), However, when these channels were activated by acid, cold temperature potentiated the currents by slowing the rate of desensitization. Potentiation was abolished by a "Deg" mutation that alters channel gating. Temperature changes in the physiologic range had prominent effects on current in cells heterologously expressing acid-gated DEG/ENaC channels, as well as in dorsal root ganglion sensory neurons. The finding that cold temperature modulates DEG/ENaC channel function may provide a molecular explanation for the widely recognized ability of temperature to modify taste sensation and mechanosensation.
引用
收藏
页码:6459 / 6463
页数:5
相关论文
共 44 条
[1]   A model of the detection of warmth and cold by cutaneous sensors through effects on voltage-gated membrane channels [J].
Adair, RK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (21) :11825-11829
[2]   Protons activate brain Na+ channel 1 by inducing a conformational change that exposes a residue associated with neurodegeneration [J].
Adams, CM ;
Snyder, PM ;
Price, MP ;
Welsh, MJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (46) :30204-30207
[3]   Neuropeptide FF and FMRFamide potentiate acid-evoked currents from sensory neurons and proton-gated DEG/ENaC channels [J].
Askwith, CC ;
Cheng, C ;
Ikuma, M ;
Benson, C ;
Price, MP ;
Welsh, MJ .
NEURON, 2000, 26 (01) :133-141
[4]  
BENOS DJ, 1995, J MEMBRANE BIOL, V143, P1
[5]  
Benson CJ, 1999, CIRC RES, V84, P921
[6]   From channels to behavior: An integrative model of NaCl taste [J].
Boughter, JD ;
Gilbertson, TA .
NEURON, 1999, 22 (02) :213-215
[7]   TEMPERATURE RECEPTORS IN THE CENTRAL-NERVOUS-SYSTEM [J].
BOULANT, JA ;
DEAN, JB .
ANNUAL REVIEW OF PHYSIOLOGY, 1986, 48 :639-654
[8]   AMILORIDE-SENSITIVE EPITHELIAL NA+ CHANNEL IS MADE OF 3 HOMOLOGOUS SUBUNITS [J].
CANESSA, CM ;
SCHILD, L ;
BUELL, G ;
THORENS, B ;
GAUTSCHI, I ;
HORISBERGER, JD ;
ROSSIER, BC .
NATURE, 1994, 367 (6462) :463-467
[9]   The capsaicin receptor: a heat-activated ion channel in the pain pathway [J].
Caterina, MJ ;
Schumacher, MA ;
Tominaga, M ;
Rosen, TA ;
Levine, JD ;
Julius, D .
NATURE, 1997, 389 (6653) :816-824
[10]   A capsaicin-receptor homologue with a high threshold for noxious heat [J].
Caterina, MJ ;
Rosen, TA ;
Tominaga, M ;
Brake, AJ ;
Julius, D .
NATURE, 1999, 398 (6726) :436-441