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. 2018 Sep 4;16(5):3951–3958. doi: 10.3892/etm.2018.6687

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Copyright: © Li et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Figure 5. — Effects of Malat1 on the apoptosis and proliferation of AEC-treated DCs. AECs were incubated with NC siRNA or Malat1 siRNA and then cocultured with DCs for 72 h. The percentage of apoptosis of (A) NC siRNA and (B) Malat1 siRNA groups. FITC-Annexin-V of DCs was detected by FASC in (C) NC siRNA and (D) Malat1 siRNA groups. (E) Protein levels of caspase-3, Bax, and Bcl-2 in DCs were detected by WB. (F) DC cell viability was determined by MTT assay. Mean ± SD calculated from five different experiments (P<0.05 vs. ‘NC siRNA’ group). AEC, airway epithelial cells; DC, dendritic cell; Malat1, metastasis-associated lung adenocarcinoma transcript 1.