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Original Article Blocking follistatin-like 1 attenuates liver fibrosis in mice by regulating transforming growth factor-beta signaling

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Academic year: 2020

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Figure

Figure 1. (A) IHC images of FSTL1 expression in human cirrhotic liver tissues (a) and normal liver tissues (b)
Figure 2. Primary HSCs isolated from mice were fixed at five days. ICC images showed that the activation of HSCs treated with IgG was faster than that of HSCs treated with FSTL1.
Figure 3. (A) Treatment of HSCs with an FSTL1 mAb had no significant effect on cell proliferation in vitro; (B) Transwell assay showed that HSC-T6 cells treated with the FSTL1 mAb (c, d) exhibited reduced migration compared with cells treated with IgG (a, b) in vitro.
Figure 4. (A) Sirius Red staining showed that CCl4-induced mice treated with an FSTL1 mAb (c, d) exhibited reduced collagen accumulation, and attenu-ation of liver fibrosis compared with CCl4-induced mice treated with IgG (a, b) in vivo; (B) Masson staining showed that treatment of CCl4-induced mice with the FSTL1 mAb (b) resulted in attenuation of liver fibrosis in vivo; (C) The ALT and AST detection results showed that treatment of mice with the FSTL1 mAb resulted in attenuation of liver injury caused by CCl4.
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