Effect of donor age on the proliferation and multipotency of canine adipose-derived mesenchymal stem cells

被引:25
作者
Lee, Jienny [1 ]
Lee, Keum Sil [1 ]
Kim, Chan-Lan [1 ]
Byeon, Jeong Su [1 ]
Gu, Na-Yeon [1 ]
Cho, In-Soo [1 ]
Cha, Sang-Ho [1 ]
机构
[1] Anim & Plant Quarantine Agcy, Viral Dis Res Div, Gimcheon 39660, South Korea
关键词
adipose mesenchymal stem cells; age; canine; differentiation; multipotency; UMBILICAL-CORD MATRIX; BONE-MARROW; IN-VITRO; CHONDROGENIC DIFFERENTIATION; TISSUE; PASSAGE; EXPRESSION; CAPACITY; DECREASE; CULTURE;
D O I
10.4142/jvs.2017.18.2.141
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Research into adipose tissue-derived mesenchymal stem cells (AD-MSCs) has demonstrated the feasibility of their use in clinical applications due to their ease of isolation and abundance in adipose tissue. We isolated AD-MSCs from young and old dogs, and the cells were subjected to sequential sub-passaging from passage 1 (P1) to P7. Canine AD-MSCs (cAD-MSCs) were examined for proliferation kinetics, expression of molecules associated with self-renewal, expression of cell surface markers, and differentiation potentials at P3. Cumulative population doubling level was significantly higher in cAD-MSCs of young donors than in those of old donors. In addition, expressions of CD73, CD80, Oct3/4, Nanog, cell survival genes and differentiation potentials were significantly higher in young donors than in old donors. The present study suggests that donor age should be considered when developing cell-based therapies for clinical application of cAD-MSCs.
引用
收藏
页码:141 / 148
页数:8
相关论文
共 36 条
[1]   Aging alters tissue resident mesenchymal stem cell properties [J].
Alt, Eckhard U. ;
Senst, Christiane ;
Murthy, Subramanyam N. ;
Slakey, Douglas P. ;
Dupin, Charles L. ;
Chaffin, Abigail E. ;
Kadowitz, Philip J. ;
Izadpanah, Reza .
STEM CELL RESEARCH, 2012, 8 (02) :215-225
[2]   Concise review: Mesenchymal stem cells: Their phenotype, differentiation capacity, immunological features, and potential for homing [J].
Chamberlain, Giselle ;
Fox, James ;
Ashton, Brian ;
Middleton, Jim .
STEM CELLS, 2007, 25 (11) :2739-2749
[3]   Bone marrow derived mesenchymal stem cells from aged mice have reduced wound healing, angiogenesis, proliferation and anti-apoptosis capabilities [J].
Choudhery, Mahmood Saba ;
Khan, Mohsin ;
Mahmood, Ruhma ;
Mehmood, Azra ;
Khan, Shaheen N. ;
Riazuddin, Sheikh .
CELL BIOLOGY INTERNATIONAL, 2012, 36 (08) :747-753
[4]   Relationship between donor age and the replicative lifespan of human cells in culture: A reevaluation [J].
Cristofalo, VJ ;
Allen, RG ;
Pignolo, RJ ;
Martin, BG ;
Beck, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (18) :10614-10619
[5]   Age-Dependent Impaired Neurogenic Differentiation Capacity of Dental Stem Cell is Associated with Wnt/β-Catenin Signaling [J].
Feng, Xingmei ;
Xing, Jing ;
Feng, Guijuan ;
Sang, Aimin ;
Shen, Biyu ;
Xu, Yue ;
Jiang, Jinxia ;
Liu, Suzhe ;
Tan, Wei ;
Gu, Zhifeng ;
Li, Liren .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 2013, 33 (08) :1023-1031
[6]   Fat tissue: an underappreciated source of stem cells for biotechnology [J].
Fraser, JK ;
Wulur, I ;
Alfonso, Z ;
Hedrick, MH .
TRENDS IN BIOTECHNOLOGY, 2006, 24 (04) :150-154
[7]   Adipose-derived adult stem cells: isolation, characterization, and differentiation potential [J].
Gimble, JM ;
Guilak, F .
CYTOTHERAPY, 2003, 5 (05) :362-369
[8]   Canine mesenchymal stem cells (MSCs): characterization in relation to donor age and adipose tissue-harvesting site [J].
Guercio, Annalisa ;
Di Bella, Santina ;
Casella, Stefania ;
Di Marco, Patrizia ;
Russo, Carmelo ;
Piccione, Giuseppe .
CELL BIOLOGY INTERNATIONAL, 2013, 37 (08) :789-798
[9]   Age-dependent decline in dental pulp regeneration after pulpectomy in dogs [J].
Iohara, Koichiro ;
Murakami, Masashi ;
Nakata, Kazuhiko ;
Nakashima, Misako .
EXPERIMENTAL GERONTOLOGY, 2014, 52 :39-45
[10]   The uric acid transporter SLC2A9 is a direct target gene of the tumor suppressor p53 contributing to antioxidant defense [J].
Itahana, Y. ;
Han, R. ;
Barbier, S. ;
Lei, Z. ;
Rozen, S. ;
Itahana, K. .
ONCOGENE, 2015, 34 (14) :1799-1810