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. 2014 May 8;140(2):271–282. doi: 10.1093/toxsci/kfu087

TABLE 3. Effects of oxidants and inflammatory stimuli on let-7a levels in HUVECs and mouse aorta.

Treatment Fold change ± SE n p
10-μM acrolein 1.42 ± 0.18 13 0.02
10-μM HNE 0.97 ± 0.08 10 >0.05
25-μM HNE 0.66 ± 0.09 3 >0.05
50-μM HNE 1.01 ± 0.04 3 >0.05
10-μM POVPC 0.82 ± 0.08 3 >0.05
10-μM acrylic acid 0.51 ± 0.14 4 0.05
10-μM allyl alcohol 0.80 ± 0.27 5 >0.05
10-μg/ml ox PAPC 0.80 ± 0.001 3 0.001
25-μg/ml ox PAPC 0.84 ± 0.11 3 >0.05
50-μg/ml ox PAPC 0.59 ± 0.36 3 >0.05
200-μM H2O2 0.92 ± 0.12 9 >0.05
10-ng/ml TNF-α 0.97 ± 0.14 5 >0.05
1-μg/ml LPS 1.08 ± 0.14 5 >0.05
Inhaled acrolein
(a) Intact aorta 1.87 ± 0.25 25 0.04
(b) denuded aorta 1.26 ± 0.03 5 >0.05

Levels of let-7a were measured in HUVECs after a 2-h treatment with the listed stimuli and a 4-h recovery period. For measurements in the aorta, the mice were exposed to 1-ppm acrolein or filtered air for 4 days and changes in let-7a were measured immediately after the end of the last exposure. The miRNA levels were measured by rtPCR. Values are fold change ± SE versus control.