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Comparison of Chondrogenic Potential in Equine Mesenchymal Stromal Cells Derived from Adipose Tissue and Bone Marrow
Authors:MARTIN A VIDAL BVSc  MS  Diplomate ACVS  SANDRA O ROBINSON BS  MANDI J LOPEZ DVM  MS  PhD  Diplomate ACVS  DANIEL B PAULSEN DVM  PhD  Diplomate ACVP  OLGA BORKHSENIOUS PhD  JILL R JOHNSON DVM  MS  Diplomate ACVIM & ABVP  RUSTIN M MOORE DVM  PhD  Diplomate ACVS  JEFFREY M GIMBLE MD  PhD
Institution:1. Equine Health Studies Program, Laboratory for Equine and Comparative Orthopedic Research, Department of Veterinary Clinical Sciences and the Departments of Pathobiological Sciences and Comparative Biomedical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA;2. Department of Veterinary Clinical Sciences, College of Veterinary Medicine, The Ohio State University, Columbus, OH;3. Stem Cell Laboratory, Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA
Abstract:Objective— To compare the chondrogenic potential of adult equine mesenchymal stem cells derived from bone marrow (MSCs) or adipose tissue (ASCs). Study Design— In vitro experimental study. Animals— Adult Thoroughbred horses (n=11). Methods— BM (5 horses; mean ±SD] age, 4±1.4 years) or adipose tissue (6 horses; mean age, 3.5±1.1 years) samples were obtained. Cryopreserved MSCs and ASCs were used for pellet cultures in stromal medium (C) or induced into chondrogenesis±transforming growth factor‐3 (TGFβ3) and bone morphogenic factor‐6 (BMP‐6). Pellets harvested after 3, 7, 14, and 21 days were examined for cross‐sectional size and tissue composition (hematoxylin and eosin), glycosaminoglycan (GAG) staining (Alcian blue), collagen type II immunohistochemistry, and by transmission electron microscopy. Pellet GAG and total DNA content were measured using dimethylmethylene blue and Hoechst DNA assays. Results— Collagen type II synthesis was predominantly observed in MSC pellets from Day 7 onward. Unlike ASC cultures, MSC pellets had hyaline‐like matrix by Day 14. GAG deposition occurred earlier in MSC cultures compared with ASC cultures and growth factors enhanced both MSC GAG concentrations (P<.0001) and MSC pellet size (P<.004) after 2 weeks in culture. Conclusion— Equine MSCs have superior chondrogenic potential compared with ASCs and the equine ASC growth factor response suggests possible differences compared with other species. Clinical Relevance— Elucidation of equine ASC and MSC receptor profiles will enhance the use of these cells in regenerative cartilage repair.
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