Fig. 6.
Fig. 6. Human cytokeratin 19 expression in the livers of injured mice that underwent human stem cell transplantation and were treated with HGF. / When NOD/SCID/β2M-null mice received transplants of human stem cells (CB- or BM-derived CD34+ cells) and were treated with CCl4 and HGF MSCs, cells expressing mRNA for the human cholangiocyte marker cytokeratin 19 (CK19) were found in the mouse liver. In the injured, HGF-treated chimeric mice, 2 bands were observed. The first was murine CK19, which comigrated with the band from the control mice that did not undergo transplantation. The second band was a human-specific band of the expected size, which comigrated with the CK19 band from a human liver control. No human CK19 was detected in the murine control liver, or in freshly isolated CD34+ hematopoietic progenitors. The first lane shows molecular weights.

Human cytokeratin 19 expression in the livers of injured mice that underwent human stem cell transplantation and were treated with HGF.

When NOD/SCID/β2M-null mice received transplants of human stem cells (CB- or BM-derived CD34+ cells) and were treated with CCl4 and HGF MSCs, cells expressing mRNA for the human cholangiocyte marker cytokeratin 19 (CK19) were found in the mouse liver. In the injured, HGF-treated chimeric mice, 2 bands were observed. The first was murine CK19, which comigrated with the band from the control mice that did not undergo transplantation. The second band was a human-specific band of the expected size, which comigrated with the CK19 band from a human liver control. No human CK19 was detected in the murine control liver, or in freshly isolated CD34+ hematopoietic progenitors. The first lane shows molecular weights.

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