Basic Research
Copyright ©2006 Baishideng Publishing Group Co.
World J Gastroenterol. Jun 28, 2006; 12(24): 3854-3858
Published online Jun 28, 2006. doi: 10.3748/wjg.v12.i24.3854
Figure 1
Figure 1 Lysozyme immunohistochemical staining of the Kupffer cells. The cytoplasms of the Kupffer cells were stained brown. The percentage of Kupffer cells in the adherent cells was over 90%.
Figure 2
Figure 2 Comparison of TNF-α production in supernatant of Kupffer cells. (n = 8, mean ± SE, aP < 0.05 compared with the next group, bP < 0.01 compared with the next group.)
Figure 3
Figure 3 Comparison of IL-1β production in supernatant of Kupffer cells. (n = 8, mean ± SE, bP < 0.01 compared with the next group.)
Figure 4
Figure 4 Immunohistochemical staining of MIP-1α in Kupffer cells in IRI group at 12 h’s interval SP × 400.
Figure 5
Figure 5 The synthesis of MIP-1α protein in Kupffer cells tested by immunohistochemical (n = 8, mean ± SE, bP < 0. 01 compared with control group).
Figure 6
Figure 6 A: Photograph of the MIP-1α mRNA expression in Kupffer cells tested by RT-PCR; B: Photograph of the GAPDH mRNA expression in Kupffer cells tested by RT-PCR.
Figure 7
Figure 7 Quantitative data of MIP-1α mRNA levels (n = 8, mean ± SE, bP < 0. 01 compared with control group).