Fig. 4.
Fig. 4. Immunoblot analysis of cyclin A, CDK2, and p27Kip-1 proteins in DAA-3 cells. / The cells were cultured for 2 and 4 days in SFM (center) alone or supplemented with either 10−6 mol/L 13-cis-RA (RA), 10−6 mol/L Dex, or a combination of these 2 drugs. For CDK2, faster migrating bands represent the phosphorylated active forms of this kinase. Dex induced a decrease in the amount of p27Kip-1 protein and a markedly contrasted p27Kip-1 up-regulation induced by RA. Dex also increased the levels of the phosphorylated active forms of CDK2 and antagonized an RA-induced decrease of CDK2 phosphorylation. Similar findings were obtained with the HDE-14 LCLs (not shown). We subjected 50 μg extract proteins from each lysate to immunoblot analysis. The cellular proteins visualized in each panel are indicated to the left.

Immunoblot analysis of cyclin A, CDK2, and p27Kip-1 proteins in DAA-3 cells.

The cells were cultured for 2 and 4 days in SFM (center) alone or supplemented with either 10−6 mol/L 13-cis-RA (RA), 10−6 mol/L Dex, or a combination of these 2 drugs. For CDK2, faster migrating bands represent the phosphorylated active forms of this kinase. Dex induced a decrease in the amount of p27Kip-1 protein and a markedly contrasted p27Kip-1 up-regulation induced by RA. Dex also increased the levels of the phosphorylated active forms of CDK2 and antagonized an RA-induced decrease of CDK2 phosphorylation. Similar findings were obtained with the HDE-14 LCLs (not shown). We subjected 50 μg extract proteins from each lysate to immunoblot analysis. The cellular proteins visualized in each panel are indicated to the left.

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