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. 2005 Mar;166(3):695–708. doi: 10.1016/s0002-9440(10)62291-2

Figure 4.

Figure 4

Liver fibrosis is worse in nfκb1−/− mice. A: Sirius red staining of liver sections at days 1 and 7 of recovery after 12 weeks of CCl4 injury. Black arrows denote collagen fibers and are representative of five nfκb1+/+ and four nfκb1−/− mice. B: Fibrosis scores expressed as average grade ± SEM of five nfκb1+/+ and four nfκb1−/− mice at days 1 and 7 of recovery. C: TaqMan analysis of procollagen I mRNA measured in 20 ng of cDNA from whole liver extracts at days 1, 3, 5, 7, and 14 after 12 weeks of CCl4 injury. The relative level of transcriptional difference was calculated and expressed as an average ± SEM from four nfκb1−/− and five nfκb1+/+ animals. Average cycle numbers were: day 1, 24.60 and 27.21; day 3, 25.63 and 27.32; day 5, 26.33 and 27.10; day 7, 27.0 and 27.87; and day 14, 31.87 and 29.88 for nfκb1−/− and nfκb1+/+, respectively. The differences were statistically significant, P = 0.0329, and were calculated using a paired t-test. D: TaqMan analysis of TIMP1 mRNA measured in 20 ng of cDNA from whole liver extracts. The relative level of transcriptional difference was calculated and expressed as an average ± SEM from four nfκb1−/− and five nfκb1+/+ animals. Average cycle numbers were: day 1, 31.42 and 33.47; day 3, 34.09 and 35.15; day 5, 34.19 and 35.14; day 7, 34.27 and 34.23; and day 14, 36.68 and 36.09 for nfκb1−/− and nfκb1+/+, respectively. The differences were statistically significant, P = 0.0302, and were calculated using a paired t-test. Original magnifications, ×100.