Abstract | OBJECTIVE: The aim of the present study was to determine if the electroporation-mediated gene transfer of SOX trio enhances the chondrogenic potential of adipose stem cells (ASCs). DESIGN: RESULTS: The gene transfer efficiency was high (approximately 70%). Transfected ASCs showed high expression of corresponding genes after 21 days, and each SOX protein was detected in ASCs transfected with the corresponding gene. The chondrogenic differentiation of ASCs, as demonstrated by GAG levels and Safranin-O staining, showed significant enhancement when SOX trio were co-transfected, while subsets with single gene transfer of SOX-5, -6, or -9 did not show significant elevation. SOX trio co-transfection enhanced COL2A1 mRNA, but did not increase COL1A1 and COL10A1 mRNA. Type II collagen protein dramatically increased, and type X collagen decreased with co-transfection of the SOX trio. When pellets were implanted in the subcutaneous pouch of SCID mice for 3 weeks, ASCs co-transfected with SOX trio demonstrated abundant proteoglycan, significantly reduced mineralization. CONCLUSION: The electroporation-mediated transfection of SOX trio greatly enhances chondrogenesis from ASCs, while decreasing hypertrophy.
|
Authors | G-I Im, H-J Kim |
Journal | Osteoarthritis and cartilage
(Osteoarthritis Cartilage)
Vol. 19
Issue 4
Pg. 449-57
(Apr 2011)
ISSN: 1522-9653 [Electronic] England |
PMID | 21251990
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Copyright | Copyright © 2011 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved. |
Chemical References |
- Biomarkers
- Glycosaminoglycans
- SOX Transcription Factors
- SOX5 protein, human
- SOX6 protein, human
- SOX9 Transcription Factor
- SOX9 protein, human
- SOXD Transcription Factors
- Collagen
|
Topics |
- Adipose Tissue
(cytology)
- Animals
- Biomarkers
(metabolism)
- Blotting, Western
- Cell Differentiation
(genetics, physiology)
- Cells, Cultured
- Chondrogenesis
(genetics, physiology)
- Collagen
(genetics, metabolism)
- Electroporation
- Glycosaminoglycans
(analysis)
- Mice
- Reverse Transcriptase Polymerase Chain Reaction
- SOX Transcription Factors
(genetics, metabolism)
- SOX9 Transcription Factor
(genetics, metabolism)
- SOXD Transcription Factors
(genetics, metabolism)
- Stem Cells
(cytology)
- Tissue Engineering
(methods)
|