Epithelial sodium channel/degenerin family of ion channels: A variety of functions for a shared structure

被引:829
作者
Kellenberger, S [1 ]
Schild, L [1 ]
机构
[1] Univ Lausanne, Inst Pharmacol & Toxicol, CH-1005 Lausanne, Switzerland
关键词
D O I
10.1152/physrev.00007.2002
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The recently discovered epithelial sodium channel (ENaC)/ degenerin (DEG) gene family encodes sodium channels involved in various cell functions in metazoans. Subfamilies found in invertebrates or mammals are functionally distinct. The degenerins in Caenorhabditis elegans participate in mechanotransduction in neuronal cells, FaNaC in snails is a ligand-gated channel activated by neuropeptides, and the Drosophila subfamily is expressed in gonads and neurons. In mammals, ENaC mediates Na+ transport in epithelia and is essential for sodium homeostasis. The ASIC genes encode proton-gated cation channels in both the central and peripheral nervous system that could be involved in pain transduction. This review summarizes the physiological roles of the different channels belonging to this family, their biophysical and pharmacological characteristics, and the emerging knowledge of their molecular structure. Although functionally different, the ENaC/DEG family members share functional domains that are involved in the control of channel activity and in the formation of the pore. The functional heterogeneity among the members of the ENaC/DEG channel family provides a unique opportunity to address the molecular basis of basic channel functions such as activation by ligands, mechanotransduction, ionic selectivity, or block by pharmacological ligands.
引用
收藏
页码:735 / 767
页数:33
相关论文
共 280 条
  • [101] A mutation causing pseudohypoaldosteronism type 1 identifies a conserved glycine that is involved in the gating of the epithelial sodium channel
    Grunder, S
    Firsov, D
    Chang, SS
    Jaeger, NF
    Gautschi, I
    Schild, L
    Lifton, RP
    Rossier, BC
    [J]. EMBO JOURNAL, 1997, 16 (05) : 899 - 907
  • [102] GRUNDER S, 1998, J AM SOC NEPHROL, V9, pA178
  • [103] Genetic interactions affecting touch sensitivity in Caenorhabditis elegans
    Gu, GQ
    Caldwell, GA
    Chalfie, M
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (13) : 6577 - 6582
  • [104] Hall DH, 1997, J NEUROSCI, V17, P1033
  • [105] Molecular basis of mechanotransduction in living cells
    Hamill, OP
    Martinac, B
    [J]. PHYSIOLOGICAL REVIEWS, 2001, 81 (02) : 685 - 740
  • [106] Hamill OP, 1996, PHARMACOL REV, V48, P231
  • [107] SINGLE-CHANNEL RECORDINGS FROM AMILORIDE-SENSITIVE EPITHELIAL SODIUM-CHANNEL
    HAMILTON, KL
    EATON, DC
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 249 (03): : C200 - C207
  • [108] A DE-NOVO MISSENSE MUTATION OF THE BETA-SUBUNIT OF THE EPITHELIAL SODIUM-CHANNEL CAUSES HYPERTENSION AND LIDDLE SYNDROME, IDENTIFYING A PROLINE-RICH SEGMENT CRITICAL FOR REGULATION OF CHANNEL ACTIVITY
    HANSSON, JH
    SCHILD, L
    LU, Y
    WILSON, TA
    GAUTSCHI, I
    SHIMKETS, R
    NELSONWILLIAMS, C
    ROSSIER, BC
    LIFTON, RP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (25) : 11495 - 11499
  • [109] HYPERTENSION CAUSED BY A TRUNCATED EPITHELIAL SODIUM-CHANNEL GAMMA-SUBUNIT - GENETIC-HETEROGENEITY OF LIDDLE SYNDROME
    HANSSON, JH
    NELSONWILLIAMS, C
    SUZUKI, H
    SCHILD, L
    SHIMKETS, R
    LU, Y
    CANESSA, C
    IWASAKI, T
    ROSSIER, B
    LIFTON, RP
    [J]. NATURE GENETICS, 1995, 11 (01) : 76 - 82
  • [110] Hille B., 1992, IONIC CHANNELS EXCIT