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. 2017 Jul 17;8(36):60312–60323. doi: 10.18632/oncotarget.19294

Table 2. The integrated optical density (IOD) and the positive expression areas of p-JNK, c-Jun, p-c-Jun, Sox-9 and COL2 measured by immunofluorescence.

NC IL-1β HBO H+I
IOD Positiveareas (μm2) IOD Positiveareas (μm2) IOD Positiveareas (μm2) IOD Positiveareas (μm2)
p-JNK 32.6±9.8 22.6±7.2 82.3±6.2* 70.4±8.8* 38.3±10.4# 25.6±12.7# 29.2±7.2# 20.4±9.2#
c-Jun 30.4±6.8 20.3±5.9 62.4±8.8* 52.6±9.8* 74.3±9.2& 69.2±10.2& 66.8±6.2& 60.8±8.2&
p-c-Jun 26.4±7.2 18.9±9.8 69.8±10.2* 58.4±12.7* 29.4±3.6# 22.4±5.8# 29.2±8.2# 20.5±8.4#
Sox-9 89.8±8.6 67.4±6.2 30.2±8.3* 29.3±9.5* 86.3±9.2# 70.4±9.8# 79.8±10.2# 66.4±12.2#
COL2 96.6±5.6 79.8±8.8 36.1±6.2* 28.2±6.2* 76.4±12.6# 72.3±10.2# 86.2±6.2# 79.6±7.4#

C, control; IL-1β, cells with 10ng/ml interleukin-1β; HBO, hyperbaric oxygen treated cells with 10ng/ml interleukin-1β; H+I, hyperbaric oxygen treated cells with 10ng/ml interleukin-1β and 40μM SP600125 (the JNK inhibitor). *P<0.05, significantly different from the control group; #P<0.05, significantly different from the IL-1β group. &P>0.05, no obviously difference from IL-1β group. Data are represented as the M±SEM of n=8. M, mean; SEM, standard error; n, sample size.