AI Article Synopsis

  • The epithelial Na channel (ENaC) consists of three main subunits, but variations in their expression have been identified in multiple tissues, including the vasculature and immune system.
  • Studies typically utilize heterologous expression systems and require precise antibodies for accurate ENaC function analysis, especially in non-epithelial contexts.
  • Our findings highlight the need for careful validation of anti-ENaC antibodies, demonstrating that a commonly used anti-α subunit antibody shows non-specific binding in kidney and lung tissues, which could lead to misleading results.

Article Abstract

The epithelial Na channel (ENaC) is traditionally composed of three subunits, although non-canonical expression has been found in various tissues including the vasculature, brain, lung, and dendritic cells of the immune system. Studies of ENaC structure and function have largely relied on heterologous expression systems, often with epitope-tagged channel subunits. Relevant in vivo physiological studies have used ENaC inhibitors, mice with global or tissue specific knockout of subunits, and anti-ENaC subunit antibodies generated by investigators or by commercial sources. Availability of well-characterized, specific antibodies is imperative as we move forward in understanding the role of ENaC in non-epithelial tissues where expression, subunit organization, and electrophysiological characteristics may differ from epithelial tissues. We report that a commonly used commercial anti-α subunit antibody recognizes an intense non-specific band on mouse whole kidney and lung immunoblots, which migrates adjacent to a less intense, aldosterone-induced full length α-subunit. This antibody localizes to the basolateral membrane of aquaporin 2 negative cells in kidney medulla. We validated antibodies against the β- and γ-subunits from the same commercial source. Our work illustrates the importance of validation studies when using popular, commercially available anti-ENaC antibodies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837423PMC
http://dx.doi.org/10.14814/phy2.15554DOI Listing

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