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induced expression of the myofibroblast marker protein α-SMA. Western blot analyses were
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performed on the lysates of serum starved LX-2 cells that were treated with LQ in the
control. Protein levels were presented as relative band intensities to control (vehicle treated)
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group. (B) Real-time PCR was assessed to investigate mRNA level of PAI-1 and MMP-2,
related proteins, LC3II. Data represents the mean ± SD from three separate experiments. * P
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