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. Author manuscript; available in PMC: 2019 Dec 21.
Published in final edited form as: Arch Toxicol. 2017 Dec 8;92(3):1049–1064. doi: 10.1007/s00204-017-2142-3

Table 1 – Effect of CAP1 silencing on RMC viability.

RMC were transfected with either a scrambled-sequence control plasmid (SC) or an siRNA targeting CAP1, as described in Materials and Methods. Cells were then treated with the indicated concentration of CdCl2 for 6 h in serum-free medium and viability was measured by the MTT assay. The results are mean ± s.d. from quadruplicate wells at each condition, in a single experiment, taking the absorbance of the Cd-free control as 100 % in each data set. In the 3rd and 5th columns, Dunnett’s post hoc test is used to compare the value obtained at each [Cd2+] to the value at [Cd2+] = 0. The last column shows the results of the Tukey post hoc test on the full data set, comparing scrambled control to silenced cells at the same [Cd2+]. NS - not significant (p > 0.05).

[Cd2+]
(μM)
SC (%) p vs [Cd]
= 0 (SC)
(Dunnett)
siRNA (%) p vs [Cd]
= 0 (si)
(Dunnett)
p, SC vs siRNA
(Tukey)
(Dunnett) (Dunnett) (Tukey)

0 99.9 ± 7.2 - 100 ± 2.8 -   -
10 109 ± 2.5 NS 107 ± 6.0 NS   NS
20 50.6 ± 6.8 < 0.01 70.7 ± 1.8 < 0.01   < 0.001
40 31.3 ± 3.2 < 0.01 51.9 ± 4.3 < 0.01   < 0.001