Beschreibung:
<jats:p>The epithelial sodium channel (ENaC) plays an important role in the alveolar epithelium by mediating Na<jats:sup>+</jats:sup> reabsorption, an essential process for resolution of pulmonary edema in acute respiratory distress syndrome (ARDS). Several proinflammatory conditions such as TNF‐α leads to a reduction of ENaC expression and activity that contributes to development of ARDS. To study how pro‐inflammatory conditions could modulate αENaC mRNA stability, we developped a Tet‐Off model that allows the specific inhibition of αENaC mRNA expression in presence of doxycycline. Using this model, we found that the half‐life (T<jats:sub>1/2</jats:sub>) for the transcript was about 1 hr. TNF‐α, a proinflammatory cytokine found in broncho‐alveolar lavage of ARDS patients, decreased T<jats:sub>1/2</jats:sub> to 15 min, suggesting that destabilisation of αENaC transcript plays an important role in downregulation of ENaC expression in pro‐inflammatory conditions. The 3’ untranslated region (3’UTR) of a mRNA plays an important role in modulating mRNA stability. αENaC mRNA 3’UTR is very long (~30% of the transcript). Using a bioinformatic approach, we could define three domains (D1, D2, D3) able to form secondary structures that were highly conserved in different species. Alveolar epithelial cells were co‐transfected with 3’UTR deletion mutants inserted in pTRE‐tight vector along with the Tet‐Off vector. Deletion of the distal part of 3’UTR (D3) leaded to stabilization of the transcript with a T<jats:sub>1/2 </jats:sub>of 2.6 hrs. A longer deletion to remove also D2 showed a T<jats:sub>1/2</jats:sub> of 4.6 hrs, while deletion of D1 decreased the half‐life to 0.5 hr. These results showed that the conserved domains have stabilizing (D1) and destabilizing (D2, D3) properties on αENaC mRNA expression. The hairpin structure of these domains could recruit RNA‐binding proteins responsible for modulation of αENaC mRNA stability. Altogether, our results suggest that modulation of αENaC mRNA stability via its 3’UTR could play an important role in regulation of ENaC expression during pro‐inflammatory conditions.</jats:p><jats:p><jats:bold><jats:italic>Grant Funding Source</jats:italic></jats:bold><jats:italic>: Supported by FRSQ, CFC and CIHR.</jats:italic></jats:p>