Promoting hepatogenic differentiation of human mesenchymal stem cells using a novel laminin-containing gelatin cryogel scaffold
Journal Article
·
· Biochemical and Biophysical Research Communications
- Institute of Medical Biotechnology, National Institute of Genetic Engineering and Biotechnology, Tehran (Iran, Islamic Republic of)
- Protein Research Center, Shahid Beheshti University, G. C, Tehran (Iran, Islamic Republic of)
- Department of Biomedical Engineering, The University of Akron, Akron, OH, 44325 (United States)
Highlights: • The gelatin cryogel was optimized for stability in cell culture medium during stem cell differentiation. • The optimized gelatin cryogel improved with the laminin, the main component of basal lamina. • The novel scaffold with laminin efficiently enhanced differentiation of mesenchymal stem cells toward hepatocyte lineage. Liver transplantation is the only definitive treatment currently available for acute and chronic liver failure. However, this approach has been restricted by complications including rejection and infection. Tissue engineering approaches using stem cell-derived functional hepatic cells offer a potential alternative. Using biologically compatible scaffolds is an important complementary key to achieve optimal construct for hepatic replacement. In the present study, to optimize the differentiation of human adipose-derived mesenchymal stem cells (ADMSCs) toward hepatocyte-like cells, a previously described gelatin cryogel was optimized and improved by laminin, the major component of basal lamina. The ADMSCs seeded on the scaffold displayed increased attachment in the presence of laminin and the MTT assay showed good compatibility for cell proliferation. The differentiation of stem cells were evaluated using glycogen staining, urea secretion measurement, hepatocyte specific cell surface analysis and gene expression analysis. The results of tests indicated that laminin protein and gelatin cryogel 3D scaffold, each on its own, enhanced hepatogenic differentiation of ADMSCs. However, when laminin immobilized on the gelatin cryogel surface, the differentiation was promoted significantly and the resulting cells showed striking similarity to HepG2 in terms of expressing studied hepatocyte markers.
- OSTI ID:
- 23134047
- Journal Information:
- Biochemical and Biophysical Research Communications, Journal Name: Biochemical and Biophysical Research Communications Journal Issue: 1-4 Vol. 507; ISSN 0006-291X; ISSN BBRCA9
- Country of Publication:
- United States
- Language:
- English
Similar Records
Transient expression of laminin {alpha}1 chain in regenerating murine liver: Restricted localization of laminin chains and nidogen-1
Differentiation within autologous fibrin scaffolds of porcine dermal cells with the mesenchymal stem cell phenotype
Assessment of the hepatocytic differentiation ability of human skin-derived ABCB5+ stem cells
Journal Article
·
Fri Apr 15 00:00:00 EDT 2005
· Experimental Cell Research
·
OSTI ID:20717580
Differentiation within autologous fibrin scaffolds of porcine dermal cells with the mesenchymal stem cell phenotype
Journal Article
·
Thu Jan 31 23:00:00 EST 2013
· Experimental Cell Research
·
OSTI ID:22215482
Assessment of the hepatocytic differentiation ability of human skin-derived ABCB5+ stem cells
Journal Article
·
Wed Aug 15 00:00:00 EDT 2018
· Experimental Cell Research
·
OSTI ID:23082680