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. 2015 Jul 29;10(7):e0129743. doi: 10.1371/journal.pone.0129743

Fig 6. Proliferation of HSCs was reduced by deficiency of NOX1 and NOX4 in response to liver injury and PDGF.

Fig 6

(A) HSC proliferation is reduced in NOX1KO and NOX4KO mice after CCl4 injury. HSC proliferation in liver was presented by PCNA immunofluorescence microscopy. Desmin is a specific marker of HSCs (Red). PCNA is a marker of proliferation (Green). Original magnification X10. (B) Proliferation was reduced in HSCs lacking NOX1 and NOX4 in response to PDGF (10 ng/ml) for 24 h. Proliferative HSCs were presented by Ki67 (Red) immunofluorescence microscopy. Nuclei were presented by DAPI (Blue). Original magnification X10. (C) Graph of PCNA-positive HSCs in vivo. (D) Graph of Ki67-positive HSCs in vitro.