Functional interaction of COMMD3 and COMMD9 with the epithelial sodium channel.

Yong Feng Liu, Marianne Swart, Ying Ke, Kevin Ly, Fiona J McDonald

Department of Physiology, University of Otago, Dunedin, New Zealand.

American journal of physiology. Renal physiology 2013 Jul 1

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The epithelial sodium channel (ENaC) plays an important role in controlling Na⁺ homeostasis, extracellular fluid volume, and blood pressure. Copper metabolism Murr1 domain-containing protein 1 (COMMD1) interacts with ENaC and downregulates ENaC. COMMD1 belongs to the COMMD family consisting of COMMD1-10, and all COMMD family members share a C-terminal COMM domain. Here, we report that COMMD2-10 also interacts with ENaC, and COMMD3 and COMMD9 were selected for further study. Amiloride-sensitive current in mammalian epithelia expressing ENaC was significantly reduced by COMMD3 or COMMD9, and ENaC expression at the cell surface was significantly decreased in the presence of COMMD3 or COMMD9. COMMD3 and COMMD9 retained their ability to reduce current when COMMD1 was knocked down. COMMD3 and COMMD9 were widely expressed in kidney and were colocalized with ENaC in renal collecting duct cells. These data suggest that COMMD3 and COMMD9 may be endogenous regulators of ENaC to regulate Na⁺ transport through altering ENaC cell surface expression.

Citation

Yong Feng Liu, Marianne Swart, Ying Ke, Kevin Ly, Fiona J McDonald. Functional interaction of COMMD3 and COMMD9 with the epithelial sodium channel. American journal of physiology. Renal physiology. 2013 Jul 1;305(1):F80-9