Exogenous increase in miR expression reduces aldosterone-stimulated ENaC transport. (A) Normalized ISC measurements from mCCD were transiently transfected with plasmids encoding pre-miR sequences, alone or in combination. Cells seeded onto filter supports were stimulated with aldosterone for 24 hours (50 nM), and ISC was normalized to unstimulated mCCD cells transfected with control plasmid. ISC response to aldosterone decreased significantly (*P<0.05) in cells overexpressing miR-1983, miR-290–5p, and miR-335–3p or the combination of the three miRs (n=30). (B) The same experiments as in A were carried out using miR mimics, and a significant reduction in aldosterone response was seen for all overexpressed miRs (n=10).