Abstract | BACKGROUND AIMS: The protocols for differentiation of hepatocyte-like cells (HLCs) from mesenchymal stromal cells (MSCs) have been well established. Previous data have shown that MSCs and their derived HLCs were able to engraft injured liver and alleviate injuries induced by carbon tetrachloride. The goal of the current study was to determine the differences of MSCs and their derived HLCs in terms of therapeutic functions in liver diseases. METHODS: RESULTS: MSC-derived-HLCs expressed lower levels of hepatocyte growth factor, accompanied by impaired immunosuppression in comparison with MSCs. Furthermore, undifferentiated MSCs showed rescuing potentials superior to those in HLCs for the treatment of fulminant hepatic failure. CONCLUSIONS: After differentiation, HLCs lost several major properties in comparison with undifferentiated MSCs, which are beneficial for their application in liver diseases. Undifferentiated MSCs may be more appropriate than are HLCs for the treatment of liver diseases.
|
Authors | Hanyu Wang, Tingting Zhao, Fang Xu, Yan Li, Mingyuan Wu, Delin Zhu, Xiuli Cong, Yongjun Liu |
Journal | Cytotherapy
(Cytotherapy)
Vol. 16
Issue 3
Pg. 309-18
(Mar 2014)
ISSN: 1477-2566 [Electronic] England |
PMID | 24239106
(Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
|
Copyright | Copyright © 2014 International Society for Cellular Therapy. All rights reserved. |
Chemical References |
- CXCR4 protein, human
- Cell Adhesion Molecules
- Receptors, CXCR4
- Hepatocyte Growth Factor
- Aspartate Aminotransferases
- Alanine Transaminase
|
Topics |
- Alanine Transaminase
(blood)
- Animals
- Aspartate Aminotransferases
(blood)
- Cell Adhesion Molecules
(metabolism)
- Cell Differentiation
- Cells, Cultured
- Hepatocyte Growth Factor
(metabolism)
- Hepatocytes
(cytology, metabolism)
- Humans
- Liver
(metabolism, pathology, surgery)
- Liver Failure, Acute
(therapy)
- Male
- Mesenchymal Stem Cell Transplantation
- Mesenchymal Stem Cells
(physiology)
- Mice
- Mice, Inbred BALB C
- Receptors, CXCR4
(metabolism)
- Umbilical Cord
(cytology)
|