Characterization and Comparison of Canine Multipotent Stromal Cells Derived from Liver and Bone Marrow

被引:14
|
作者
Malagola, Ermanno [1 ,2 ]
Teunissen, Michelle [1 ]
van der Laan, Luc J. W. [3 ]
Verstegen, Monique M. A. [3 ]
Schotanus, Baukje A. [1 ]
van Steenbeek, Frank G. [1 ]
Penning, Louis C. [1 ]
van Wolferen, Monique E. [1 ]
Tryfonidou, Marianna A. [1 ]
Spee, Bart [1 ]
机构
[1] Univ Utrecht, Fac Vet Med, Dept Clin Sci Compan Anim, NL-3584 CM Utrecht, Netherlands
[2] Univ Zurich Hosp, Dept Visceral & Transplantat Surg, Swiss Hepatopancreatobiliary Ctr, CH-8091 Zurich, Switzerland
[3] Erasmus MC Univ Med Ctr, Dept Surg, Rotterdam, Netherlands
关键词
MESENCHYMAL STEM-CELLS; IN-VITRO; INTERNATIONAL-SOCIETY; PROGENITOR CELLS; THERAPY; MUSCLE; DIFFERENTIATION; TISSUE; DISEASE; REPAIR;
D O I
10.1089/scd.2015.0125
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Liver-derived multipotent stromal cells (L-MSCs) may prove preferable for treatment strategies of liver diseases, in comparison to the widely studied bone marrow-derived MSCs (BM-MSCs). Canines are a large animal model, in which the pathologies of liver diseases are similar to man. This study further promotes the implementation of canine models in MSC-based treatments of liver diseases. L-MSCs were characterized and compared to BM-MSCs from the same individual. Both cell types demonstrated a spindle-shaped fibroblast-like morphology, possessed the same growth potential, and demonstrated similar immunomodulation gene expression of CD274, PTGS-1, and PTGS-2. Marked differences in cell surface markers, CD105 and CD146, distinguished these two cell populations, and L-MSCs retained a liver-specific imprinting, observed by expression of CK18 and CK19. Finally, both populations differentiated toward the osteogenic and adipogenic lineage; however, L-MSCs failed to differentiate into the chondrogenic lineage. In conclusion, characterization of canine L-MSCs and BM-MSCs demonstrated that the two cell type populations are highly comparable. Although it is still unclear which cell source is preferred for clinical application in liver treatment strategies, this study provides a foundation for future controlled studies with MSC therapy in various liver diseases in dogs before their application in man.
引用
收藏
页码:139 / 150
页数:12
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