Fig. 4.
m-NG2/BMMSCs homed to lesions, differentiated into BDCs and promoted host BDC-mediated hepatocyte regeneration as a core component of m-BMMSC functions. (A) CFSE-labeled m-NG2/BMMSCs and m-BMMSCs migrated into injured areas of the liver 72 h after transplantation. (B) Quantitative analysis of the data in A (boxes, n = 6). (Ca-c) IF staining of CK19+ cells (red) differentiated from CFSE-labeled m-NG2/BMMSCs (a) and m-BMMSCs (b) and quantification (c, merged, n = 6, the. The boxes represent CK19+ cells that formed vessel-like structures). (Da-c) Double IF staining of host CK19+ cells (green, arrows) after 72 h covered by ALB+ cells (red) in mice (livers) treated with m-NG2/BMMSCs (a) or m-BMMSCs (b) and quantification of the merged cells (arrows, c, n = 6). (Ea-c) Analysis of CK7 by IF staining (red) (a, b) and mRNA levels using RT‒qPCR (c); n = 6. (Fa-c) Similar analysis to E for CK19, n = 6. The data are presented as the means ± SDs from several independent experiments. Scale bar = 200 μm. **P < 0.001 compared with m-BMMSCs; ns represents no significant difference
