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©2013 Baishideng Publishing Group Co.
World J Biol Chem. May 26, 2013; 4(2): 18-29
Published online May 26, 2013. doi: 10.4331/wjbc.v4.i2.18
Published online May 26, 2013. doi: 10.4331/wjbc.v4.i2.18
Figure 6 High-mobility group box 1/2/3 pathway did not involved in 5,6-dimethylxanthenone-4-acetic acid-induced interferon-β expression.
A-C: C10 cells were transfected with control small interfering RNA (siRNA) or high-mobility group box 1/2/3 (HMGB1/2/3) siRNA, the relative of each HMGB mRNA level was measured by real time reverse transcription-polymerase chain reaction (RT-PCR), respectively, HMGB1, HMGB2 and HMGB3; D: C10 cells were transfected with control siRNA or HMGB1/2/3 siRNA, then cells were further incubated with or without DMXAA or Poly I-C. The relative interferon (interferon) mRNA levels were measured by real time RT-PCR (bP < 0.01 vs HMGB1/2/3 siRNA; dP < 0.01 vs HMGB1/2/3 siRNA in Poly I-C group).
- Citation: Yu Z, Predina JD, Cheng G. Refractoriness of interferon-beta signaling through NOD1 pathway in mouse respiratory epithelial cells using the anticancer xanthone compound. World J Biol Chem 2013; 4(2): 18-29
- URL: https://www.wjgnet.com/1949-8454/full/v4/i2/18.htm
- DOI: https://dx.doi.org/10.4331/wjbc.v4.i2.18