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. 2018 Jun 21;10(7):e8643. doi: 10.15252/emmm.201708643

Figure 7. Vtn‐dependent B220+CD11c+NK1.1+HepEL attachment to fibrinogen.

Figure 7

  • A
    Adhesion assay of B220+CD11c+NK1.1+ cells to fibrinogen‐coated plates. The rhodamine‐labelled liver B220+CD11c+NK1.1+ cells were separately cultured with TCM‐stimulating liver tissues and seeded on a fibrinogen‐coated plate.
  • B
    Relative mRNA levels of FX, Vtn and TSP1 in liver B220+CD11c+NK1.1+ cells stimulated with LiCM or LuCM. Shown are averages (N = 6/group) with SEM and one‐way ANOVA.
  • C
    Relative mRNA levels of FX in liver B220+CD11c+NK1.1+ cells stimulated with various factors. Shown are averages (N = 4) with SEM and one‐way ANOVA.
  • D
    In vitro adhesion assay. Liver B220+CD11c+NK1.1+ cells were seeded on a fibrinogen plate. Cells attached to the plate were counted. Twenty μg/ml of anti‐Vtn Ab or isotype control IgG was used to block the adhesion. Shown are averages (N = 6/group) with SEM and one‐way ANOVA.
  • E
    Lung B220+CD11c+NK1.1+ cells were seeded on ECM‐coated (fibrinogen, fibronectin or collagen I) plates. Shown are averages (N = 5/group) with SEM and one‐way ANOVA.