<p>Primary mouse HSCs were treated with TGF-β1 or PDGF, along with or without increasing doses of PQQ or NAC. (A, B) The level of intracellular ROS was measured by DCFH-DA staining and flow cytometry analysis. (C) Protein expression of α-SMA and collagen 1A1 in HSCs were examined by western blot analysis to evaluate the level of HSCs transdifferentiation and collagen 1A1 production after 24 h treatment of TGF-β1. (D) Primary HSCs were applied to CCK8 assay. (E, F) Primary HSCs were applied to transwell assay. *, p<0.05, **, p<0.01.</p
<p>(A-B) Frozen liver sections were stained with DHE (A), and average fluorescence unit was calculat...
(A) Measurement of pharmacological inhibitors on TGFβ1 signaling. Cells were pretreated with the ind...
<p>(A) hTERT-HSCs were exposed to 1–5 ng/mL TGF-β1 for 48 hours. mRNA was extracted using TRIzol con...
<p>(A) Liver sections were stained with RACK1 (red) and α-SMA (green) antibodies. Scale bar, 100 μm....
<p>(A) HSCs isolated from WT mice were loaded with H2DCFDA (10 μM) for 20 min. Cells were then washe...
<p>(A) Primary mouse HSCs were serum-starved for 6 h, and treated with TGF-β1 (10 ng/ml) for indicat...
<p>(A) LX-2 cells and the isolated primary rat HSCs were treated with increasing concentrations of N...
<p>(A-B) hTERT-HSCs (A) and primary HSCs (B) were transfected for 72 hours with siNrf2, siKeap1 or s...
<p>After treatment with TGF-β1 (1 ng/ml) alone or with PTHrP (100 nM) for 48 h, collagen I (138 kd) ...
<p>A) CTGF mRNA expression of HSC treated with IL-6 (10 ng/ml), TGF-β (4 ng/ml) ± UDCA-LPE (50/90 μM...
<p>(A) Flag-hPP2Cα, shPP2Cα494 and control vectors were electransfected into LX-2 cells. At 48 h pos...
<p>(A,B) LX-2 cells and the isolated primary rat HSCs were treated with increasing concentrations of...
<p>LX-2 were co-cultured with TGF-β (2.5 ng/ml) for 12 hours, subsequently stimulated with CXCL9 (2 ...
<p>(A) Western blot analysis of signaling pathways in BM-MSCs mono-culture. BM-MSCs were incubated w...
<p>(A) SB431542 suppresses the increase in α-SMA but not the decrease in E-cadherin in PQ-treated ce...
<p>(A-B) Frozen liver sections were stained with DHE (A), and average fluorescence unit was calculat...
(A) Measurement of pharmacological inhibitors on TGFβ1 signaling. Cells were pretreated with the ind...
<p>(A) hTERT-HSCs were exposed to 1–5 ng/mL TGF-β1 for 48 hours. mRNA was extracted using TRIzol con...
<p>(A) Liver sections were stained with RACK1 (red) and α-SMA (green) antibodies. Scale bar, 100 μm....
<p>(A) HSCs isolated from WT mice were loaded with H2DCFDA (10 μM) for 20 min. Cells were then washe...
<p>(A) Primary mouse HSCs were serum-starved for 6 h, and treated with TGF-β1 (10 ng/ml) for indicat...
<p>(A) LX-2 cells and the isolated primary rat HSCs were treated with increasing concentrations of N...
<p>(A-B) hTERT-HSCs (A) and primary HSCs (B) were transfected for 72 hours with siNrf2, siKeap1 or s...
<p>After treatment with TGF-β1 (1 ng/ml) alone or with PTHrP (100 nM) for 48 h, collagen I (138 kd) ...
<p>A) CTGF mRNA expression of HSC treated with IL-6 (10 ng/ml), TGF-β (4 ng/ml) ± UDCA-LPE (50/90 μM...
<p>(A) Flag-hPP2Cα, shPP2Cα494 and control vectors were electransfected into LX-2 cells. At 48 h pos...
<p>(A,B) LX-2 cells and the isolated primary rat HSCs were treated with increasing concentrations of...
<p>LX-2 were co-cultured with TGF-β (2.5 ng/ml) for 12 hours, subsequently stimulated with CXCL9 (2 ...
<p>(A) Western blot analysis of signaling pathways in BM-MSCs mono-culture. BM-MSCs were incubated w...
<p>(A) SB431542 suppresses the increase in α-SMA but not the decrease in E-cadherin in PQ-treated ce...
<p>(A-B) Frozen liver sections were stained with DHE (A), and average fluorescence unit was calculat...
(A) Measurement of pharmacological inhibitors on TGFβ1 signaling. Cells were pretreated with the ind...
<p>(A) hTERT-HSCs were exposed to 1–5 ng/mL TGF-β1 for 48 hours. mRNA was extracted using TRIzol con...