4.5 Review Book Chapter

The Contribution of Epithelial Sodium Channels to Alveolar Function in Health and Disease

Journal

ANNUAL REVIEW OF PHYSIOLOGY
Volume 71, Issue -, Pages 403-423

Publisher

ANNUAL REVIEWS
DOI: 10.1146/annurev.physiol.010908.163250

Keywords

ENaC; alveolar type 1 cells; alveolar type 2 cells; lung slice; CFTR; nonselective cation channels; single-channel recording

Categories

Funding

  1. [R2413K064399]
  2. [R37DK037963]
  3. [K99/R00HL092226]
  4. [R01HL071621]
  5. [R01HL063306]
  6. [T32DK07656]
  7. [R01HL083120]
  8. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [K99HL092226, R01HL071621, R01HL063306, R01HL083120] Funding Source: NIH RePORTER
  9. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R37DK037963, R24DK064399, T32DK007656] Funding Source: NIH RePORTER

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Amiloride-sensitive epithelial sodium channels (ENaC) play an important role in lung sodium transport. Sodium transport is closely regulated to maintain an appropriate fluid layer on the alveolar surface. Both alveolar type I and H cells have several different sodium-permeable channels in their apical membranes that play a role in normal lung physiology and pathophysiology In many epithelial tissues, ENaC is formed from three subunit proteins: alpha, beta, and gamma ENaC. Part of the diversity of sodium-permeable channels in lung arises from assembling different combinations of these subunits to form channels with different biophysical properties and different mechanisms for regulation. Thus, lung epithelium has enormous flexibility to alter the magnitude of salt and water transport. In lung, ENaC is regulated by many transmitter and hormonal agents. Regulation depends upon the type of sodium channel but involves controlling the number of apical channels and/or the activity of individual channels.

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