Skip to main content
. 2018 Aug 24;37(18):e98358. doi: 10.15252/embj.201798358

Figure 8. TRIM16 reduces cytotoxicity mediated by oxidative and proteotoxic stresses.

Figure 8

  • A
    MTT assays performed at different time points with HeLa and TRIM16KO cells, untreated or treated with H2O2 (400 μM, 2 h). Data, mean ± SD, n = 3, *P < 0.05 (Student's unpaired t‐test).
  • B
    Images of HeLa and TRIM16KO cells, untreated or treated with As2O3 (2.5 μM, 4 h). Scale bar: 400 μm.
  • C–F
    Flow cytometry analysis of HeLa and TRIM16KO cells stained with Annexin‐V/propidium iodide (double‐staining), untreated or treated with (C) As2O3 (2.5 μM, 4 h), (D) H2O2 (400 μM, 2 h), (E) puromycin (5 μg/ml, 6 h), and (F) MG132 (20 μM, 8 h).
  • G
    Immunoblot blot analysis of HeLa and TRIM16KO lysates of cells treated with 5 μM of As2O3 for different durations as indicated and probed with antibodies as shown. L.E, low exposure; H.E, high exposure. Arrowheads indicate the cleaved form of PARP‐1 and caspase‐3.

Source data are available online for this figure.