1. Central Laboratory Peking University Shenzhen Hospital
2. Central Laboratory Peking University Shenzhen Hospital Shenzhen,518036
3. ,China
纸质出版:2006
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Conversion of mononuclear cells from human umbilical cord blood into hepatocyte-like cells[J]. 解放军医学杂志(英文版), 2006,(6):358-364.
[1]张芳婷,房家智,于洁,万汇涓,叶静,龙霞,尹美珺,黄春桥.Conversion of mononuclear cells from human umbilical cord blood into hepatocyte-like cells[J].Journal of Medical Colleges of PLA,2006(06):358-364.
Conversion of mononuclear cells from human umbilical cord blood into hepatocyte-like cells[J]. 解放军医学杂志(英文版), 2006,(6):358-364. DOI:
[1]张芳婷,房家智,于洁,万汇涓,叶静,龙霞,尹美珺,黄春桥.Conversion of mononuclear cells from human umbilical cord blood into hepatocyte-like cells[J].Journal of Medical Colleges of PLA,2006(06):358-364. DOI:
<正>Objective: To evaluate the differentiation of human umbilical cord blood cells into hepatocyte-like cells. Methods: Mononuclear cells (MNCs) derived from human umbilical cord blood were isolated using Ficoll. The experiment was derived into 3 categories:(1) MNCs co-cultured with 50 mg minced liver tissue separated by a trans-well membrane and then collected at 0 h
24 h
48 h and 72 h; (2) MNCs cultured along supplemented with 100 ml/L FBS. 100μ/ml penicillin
100μg/ml streptomycin. 4. 7μg/ml linoleic acid
1×ITS
10-4 mol/L L-Ascorbic acid 2-P and a combination of FGF4 (100 ng/ml) and HGF (20 ng/mL). Cells were then collected at 0 d and 16 d to examine the expression profile of hepatocyte correlating markers;(3) 0. 2-0. 3 ml of MNCs with a cell density of 2×107/ml were transplanted into prepared recipient mice [n = 12
injected with 0. 4 ml/kg (20%) CCl4 and 150 ng/kg 5-fluorouracil (5-Fu) prior the transplant 24 h and 48 h
respectively] via injection through tail vein. Mice were sacrificed 4 weeks after transplantation. The hepatocyte correlating mRNAs and proteins were determined by RT-PCR
immunohistochemical analysis and immunoflurence technique. Results: (1) After 72 h. a number of glycogen positive stained cells were observed with MNCs co-cultured with damaged mouse liver tissues. The expression of hepatocyte markers
human albumin (ALB)
α-fetal protein (AFP) and human GATA4 mRNA and proteins were detected by RT-PCR and immunohistochemistry as well. For the confirmation
the DNA sequencing of PCR products was performed. In control groups
MNCs co-cultured with normal mouse hepatocytes or MNCs cultured alone
all markers remained negative. (2) In growth factor supplemented culture system
MNCs developed into larger volume with richer cytoplasm and binucleation after 16 d. Positive expression of ALB
AFP
CK18 and CK19 mRNA were detected with RT-PCR
and ALB positive staining was observed by immunocytochemistry as well. In contrast. MNCs cultured without exogenous growth factors scarcely attached to the culture dish and ALB mRNA was not detected. (3) In transplantation experiment
both of ALB and AFP mRNA were detected by RT-PCR and HSA
PCNA and ALB positive staining were observed in the livers of recipient mice by immunocytochemistry. Conclusion: MNCs from human umbilical cord blood could convert into hepatocyte-like cells in 3 different ways
indicating their potential use in the clinic applications for the treatment of human liver diseases.
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