posted on 2015-10-30, 00:00authored byC. Lee, A. Jones, D. Kainz, F. Khan, M.D. Carrithers
Recent work demonstrated that a splice variant of a human macrophage voltage-gated sodium
channel expressed on endosomes acts as an intracellular sensor for dsRNA, a viral-associated
molecular pattern. Here our goal was to identify a candidate gene in a clinically relevant
invertebrate model with related cellular and pattern recognition properties. The para gene in
drosophila and other insects encodes voltage-gated sodium channels with similar
electrophysiological properties to those found in vertebrate excitable membranes. A database
search revealed that the AAEL006019 gene in Aedes aegypti, the yellow fever mosquito, encodes
a voltage-gated sodium channel that is distinct from genes that encode para-like sodium
channels. As compared to para-like channels, the protein products from this gene have deletions
in the N-terminus and in the DII-DIII linker region. When over-expressed in an Aedes aegypti
cell line, CCL-125, the AAEL006019 channel demonstrated cytoplasmic expression on vesicularlike
organelles. Electrophysiologic analysis revealed that the channel mediates small inward
currents that are enhanced by synthetic mimics of viral-derived ssRNA, R848 and ORN02, but
not the dsRNA mimic, poly I:C. R848 treatment of CCL-125 cells that express high levels of the
channels led to increased expression of RelA and Ago2, two mediators of insect innate
immunity. These results suggest that the AAEL006019 channel acts as an intracellular pathogen
sensor for ssRNA molecular patterns.
History
Publisher Statement
This is the author’s version of a work that was accepted for publication in Biochemical and Biophysical Research Communications. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Biochemical and Biophysical Research Communications, 2015. 463(4): 1203-1209. DOI: 10.1016/j.bbrc.2015.06.085.