Effects of Donor Characteristics and Ex Vivo Expansion on Canine Mesenchymal Stem Cell Properties: Implications for MSC-Based Therapies

被引:45
作者
Volk, Susan W. [1 ,2 ]
Wang, Yanjian [1 ]
Hankenson, Kurt D. [2 ]
机构
[1] Univ Penn, Sch Vet Med, Dept Clin Studies, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Vet Med, Dept Anim Biol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
Mesenchymal stem cell (MSC); Regenerative medicine; Veterinary cell therapy; Canine; Tissue engineering; Aging; MARROW STROMAL CELLS; AGE-RELATED-CHANGES; GROWTH-KINETICS; BONE; DIFFERENTIATION; TRANSPLANTATION; REPAIR; SITE;
D O I
10.3727/096368912X636821
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Clinical trials utilizing bone marrow-derived mesenchymal stem cell (BM-MSC) therapies show promise for treating a variety of pathologic conditions. Paramount to optimization of such cell-based therapies is a thorough understanding of MSC biology. Despite the tremendous potential that exists for the clinical use of canine BM-MSCs in veterinary medicine, as well as in preclinical studies for human medicine, relatively little information exists regarding basic biological properties of the cells. In this study, we compared the importance of donor characteristics (age and harvest site) and ex vivo expansion on canine BM-MSC frequency (CFU-f) and differentiation potential. Advancing age was found to have a negative effect on CFU-f as well as osteogenic potential. Site of harvest was also found to have significant effects on MSC properties. MSCs obtained from the humerus were found at the lowest frequency and were least osteogenic compared to those harvested from the tibia, femur, and ilium. Osteogenic potential diminished significantly by the third passage. These results suggest important donor parameters and culture effects to consider in translational studies examining MSC-based regenerative medical strategies.
引用
收藏
页码:2189 / 2200
页数:12
相关论文
共 53 条
[1]   Evaluation of equine peripheral blood apheresis product, bone marrow, and adipose tissue as sources of mesenchymal stem cells and their differentation potential [J].
Ahern, Benjamin J. ;
Schaer, Thomas P. ;
Terkhorn, Shawn P. ;
Jackson, Karen V. ;
Mason, Nicola J. ;
Hankenson, Kurt D. .
AMERICAN JOURNAL OF VETERINARY RESEARCH, 2011, 72 (01) :127-133
[2]   Skeletal site-specific characterization of orofacial and iliac crest human bone marrow stromal cells in same individuals [J].
Akintoye, Sunday O. ;
Lam, Thanh ;
Shi, Songtao ;
Brahim, Jaime ;
Collins, Michael T. ;
Robey, Pamela G. .
BONE, 2006, 38 (06) :758-768
[3]   Allogeneic mesenchymal stem cells regenerate bone in a critical-sized canine segmental defect [J].
Arinzeh, TL ;
Peter, SJ ;
Archambault, MP ;
van den Bos, C ;
Gordon, S ;
Kraus, K ;
Smith, A ;
Kadiyala, S .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2003, 85A (10) :1927-1935
[4]   Repair of patellar tendon injuries using a cell-collagen composite [J].
Awad, HA ;
Boivin, GP ;
Dressler, MR ;
Smith, FNL ;
Young, RG ;
Butler, DL .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2003, 21 (03) :420-431
[5]   Pretreatment of adult bone marrow mesenchymal stem cells with cardiomyogenic growth factors and repair of the chronically infarcted myocardium [J].
Bartunek, Jozef ;
Croissant, Jeffrey D. ;
Wijns, William ;
Gofflot, Stephanie ;
de Lavareille, Aurore ;
Vanderheyden, Marc ;
Kaluzhny, Yulia ;
Mazouz, Naima ;
Willemsen, Philippe ;
Penicka, Martin ;
Mathieu, Myrielle ;
Homsy, Christian ;
De Bruyne, Bernard ;
McEntee, Kathleen ;
Lee, Ike W. ;
Heyndrickx, Guy R. .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2007, 292 (02) :H1095-H1104
[6]   Study of telomere length reveals rapid aging of human marrow stromal cells following in vitro expansion [J].
Baxter, MA ;
Wynn, RF ;
Jowitt, SN ;
Wraith, JE ;
Fairbairn, LJ ;
Bellantuono, I .
STEM CELLS, 2004, 22 (05) :675-682
[7]  
Bergman RJ, 1996, J BONE MINER RES, V11, P568
[8]   Control of selection bias in parallel-group controlled clinical trials in dogs and cats: 97 trials (2000-2005) [J].
Brown, Dorothy Cimino .
JAVMA-JOURNAL OF THE AMERICAN VETERINARY MEDICAL ASSOCIATION, 2006, 229 (06) :990-993
[9]  
Bruder SP, 1997, J CELL BIOCHEM, V64, P278, DOI 10.1002/(SICI)1097-4644(199702)64:2<278::AID-JCB11>3.0.CO
[10]  
2-F