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ATCC
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ATCC
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ATCC
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China Center for Type Culture Collection
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THLE-3 cell line was derived from primary normal liver cells by infection with SV40 large T antigen. The cells express cytokeratin 18 and albumin in early passage, whereas higher-passage cells in logarithmic-phase growth also express
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Image Search Results
Journal: International journal of molecular sciences
Article Title: Atezolizumab Induces Necroptosis and Contributes to Hepatotoxicity of Human Hepatocytes.
doi: 10.3390/ijms241411694
Figure Lengend Snippet: Figure 1. Human hepatocytes express PD-L1 but not PD-1 and CTLA-4. (A) The levels of PD-L1 expression were evaluated by Western blotting in whole cell lysates (WCLs) of human primary hepatocytes (HPH) and human hepatocytes (THLE-2 cells). (B) The levels of PD-L1 were evaluated by Western blotting in WCLs of THLE-2, JIMT1, and MDA-MB-231 cells. (C) The levels of PD-L1, PD-1, and CTLA-4 expression were evaluated by Western blotting in WCLs of activated T cells and THLE-2 cells after 24 h after treatment of 100 µg/mL ipilimumab (IPIL), nivolumab (NIV), and left untreated. Western blotting panels shown in this figure are representative of at least two or three independent experiments.
Article Snippet:
Techniques: Expressing, Western Blot
Journal: International journal of molecular sciences
Article Title: Atezolizumab Induces Necroptosis and Contributes to Hepatotoxicity of Human Hepatocytes.
doi: 10.3390/ijms241411694
Figure Lengend Snippet: Figure 2. Atezolizumab alone causes cytotoxicity in human hepatocytes. (A) The levels of LDH released in the cell culture medium of human primary hepatocytes (HPH) were measured after the cells were treated with indicated concentration of ATE for 24 h. (B) The levels of LDH released in the cell culture medium of THLE-2 were measured after the cells were treated with indicated concentrations of ATE for 5, 24, and 48 h. (C) Cell viability was examined using MTT assay in THLE-2 cells after the cells were treated with indicated concentrations of ATE for 48 h. (D) Cell growth was examined in THLE-2 cells after the cells were treated with indicated concentrations of ATE for 48 h. (E) Cell growth was examined in THLE-3 cells after the cells were treated with indicated concentrations of ATE for 48 h. Hepatocyte cytotoxicity assays shown in this figure are representative of at least two or three independent experiments. * p-value < 0.05, ** p-value < 0.01, *** p-value < 0.001, **** p-value < 0.0001, and ns indicates no significant change.
Article Snippet:
Techniques: Cell Culture, Concentration Assay, MTT Assay
Journal: International journal of molecular sciences
Article Title: Atezolizumab Induces Necroptosis and Contributes to Hepatotoxicity of Human Hepatocytes.
doi: 10.3390/ijms241411694
Figure Lengend Snippet: Figure 3. Phosphorylated RIP3 and MLKL are increased in atezolizumab-treated human hepatocytes (THLE-2 cells) in a dose-dependent manner. (A) The levels of phosphorylated RIP3, RIP3, phospho- rylated MLKL, and MLKL expression were evaluated by Western blotting in WCLs of THLE-2 cells after the cells were treated with either indicated concentrations of ATE or left untreated as a control.
Article Snippet:
Techniques: Expressing, Western Blot, Control
Journal: International journal of molecular sciences
Article Title: Atezolizumab Induces Necroptosis and Contributes to Hepatotoxicity of Human Hepatocytes.
doi: 10.3390/ijms241411694
Figure Lengend Snippet: Figure 4. T-cell-derived conditioned medium (T−CM) enhances expression level of PD−L1 but not CTLA−4 in human hepatocytes (THLE−2 cells). (A) The levels of PD−L1, phosphorylated Akt (T308 and S473), total Akt, phosphorylated STAT1 (Y701 and Y727), and total STAT1 expression were evaluated
Article Snippet:
Techniques: Derivative Assay, Expressing
Journal: International journal of molecular sciences
Article Title: Atezolizumab Induces Necroptosis and Contributes to Hepatotoxicity of Human Hepatocytes.
doi: 10.3390/ijms241411694
Figure Lengend Snippet: Figure 5. Both atezolizumab and T-CM induce necrosome formation in human hepatocytes (THLE-2 cells), and in turn, the induced necrosome causes hepatotoxicity in THLE-2 cells. (A) The levels of phosphorylated RIP3, RIP3, and PD-L1 expression were evaluated by Western blotting in WCLs of
Article Snippet:
Techniques: Expressing, Western Blot