Differentiation of human umbilical cord blood stem cells into hepatocytes in vivo and in vitro

• Published in: World journal of gastroenterology : WJG Vol. 12; no. 25; pp. 4014 - 4019
• Main Authors: Tang, Xiao-Peng, Zhang, Min, Yang, Xu, Chen, Li-Min, Zeng, Yang
• Format: Journal Article
• Language: English
• Published: United States Research Center of Liver Diseases, the Second Xiangya Hospital, Central South University, Changsha 410011, Hunan Province, China 07.07.2006; Baishideng Publishing Group Co., Limited
• Subjects: Albumins - metabolism; alpha-Fetoproteins - metabolism; Animals; Anticoagulants - pharmacology; Basic Research; Cell Differentiation; Cord Blood Stem Cell Transplantation; Hepatocyte Growth Factor - pharmacology; Hepatocytes - cytology; Humans; Immunohistochemistry; Liver Extracts - pharmacology; Rats; Rats, Sprague-Dawley; Stem Cells - cytology; Stem Cells - drug effects; Stem Cells - physiology; 干细胞; 细胞分化; 细胞移植; 肝细胞; 脐带血; Liver failure; Umbilical cord blood; Cell differentiation; Stem cell; Cell transplantation
• ISSN: 1007-9327; 2219-2840
• DOI: 10.3748/wjg.v12.i25.4014

AIM： To study the condition and potentiality of human umbilical cord blood stem cells （HUCBSC） to differentiate into hepatocytes in vivo or in vitro. METHODS： In a cell culture study of human umbilical cord blood stem cell （HUCBSC） differentiation, human umbilical cord blood mononuclear cells （HUCBMNC） were separated by density gradient centrifugation. Fibroblast growth factor （FGF） and hepatocyte growth factor （HGF） and the supernatant of fetal liver were added in the inducing groups. Only FGF was added in the control group. The expansion and differentiation of HUCBMNC in each group were observed. Human alpha fetoprotein （AFP） and albumin （ALB） were detected by immunohistochemistry. In the animal experiments, the survival SD rats with acute hepatic injury after carbon tetrachloride （CCL4） injection 48 h were randomly divided into three groups. The rats in group A were treated with human umbilical cord blood serum. The rats in group B were treated with HUCBMNC transplantation. The rats in group C were treated with HUCBMNC transplantation followed by intraperitoneal cyclophosphamide for 7 d. The rats were killed at different time points after the treatment and the liver tissue was histopathologically studied and human AFP and ALB detected by immunohistochemistry. The human X inactive-specific transcript gene fragment in the liver tissue was amplified by PCR to find human DNA. RESULTS： The results of cell culture showed that adherent cells were stained negative for AFP or ALB in control group. However, the adherent cells in the inducing groups stained positive for AFP or ALB. The result of animal experiment showed that no human AFP or ALB positive cells present in the liver tissue of group A （control group）. However, many human AFP or ALB positive cells were scattered around sinus hepaUcus and the central veins of hepatic Iobules and in the portal area in group B and group C after one month. The fragment of human X chromagene could be detected in the liver tissue of groups B and C, but not in group A. CONCLUSION： Under certain conditions HUCBSC can differentiate into liver cells in vivo and in vitro.