Comparative Evaluation of Human Mesenchymal Stem Cells of Fetal (Wharton's Jelly) and Adult (Adipose Tissue) Origin during Prolonged In Vitro Expansion: Considerations for Cytotherapy

被引:94
作者
Christodoulou, I. [1 ]
Kolisis, F. N. [2 ]
Papaevangeliou, D. [3 ]
Zoumpourlis, V. [1 ]
机构
[1] NHRF, Inst Biol Med Chem & Biotechnol, Athens 11635, Greece
[2] Natl Tech Univ Athens, Sch Chem Engn, Athens 15780, Greece
[3] NHRF, TAK EIE Stem Cell Bank SA, Athens 11635, Greece
关键词
UMBILICAL-CORD BLOOD; STROMAL CELLS; BONE-MARROW; CULTURE-CONDITIONS; SENESCENCE; CAPACITY; LENGTH;
D O I
10.1155/2013/246134
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
Mesenchymal stem cells (MSCs) are somatic cells with a dual capacity for self-renewal and differentiation, and diverse therapeutic applicability, both experimentally and in the clinic. These cells can be isolated from various human tissues that may differ anatomically or developmentally with relative ease. Heterogeneity due to biological origin or in vitro manipulation is, nevertheless, considerable and may equate to differences in qualitative and quantitative characteristics which can prove crucial for successful therapeutic use. With this in mind, in the present study we have evaluated the proliferation kinetics and phenotypic characteristics of MSCs derived from two abundant sources, that is, fetal umbilical cord matrix (Wharton's jelly) and adult adipose tissue (termed WJSC and ADSC, resp.) during prolonged in vitro expansion, a process necessary for obtaining cell numbers sufficient for clinical application. Our results show that WJSC are derived with relatively high efficiency and bear a substantially increased proliferation capacity whilst largely sustaining the expression of typical immunophenotypic markers, whereas ADSC exhibit a reduced proliferation potential showing typical signs of senescence at an early stage. By combining kinetic with phenotypic data we identify culture thresholds up to which both cell types maintain their stem properties, and we discuss the practical implications of their differences.
引用
收藏
页数:12
相关论文
共 54 条
[1]
FORMATION OF MINERALIZED NODULES BY BONE DERIVED CELLS-INVITRO - A MODEL OF BONE-FORMATION [J].
BERESFORD, JN ;
GRAVES, SE ;
SMOOTHY, CA .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 45 (02) :163-178
[2]
Taking Stem Cells to the Clinic: Major Challenges [J].
Bongso, Ariff ;
Fong, Chui-Yee ;
Gauthaman, Kalamegam .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2008, 105 (06) :1352-1360
[3]
Bruder SP, 1997, J CELL BIOCHEM, V64, P278, DOI 10.1002/(SICI)1097-4644(199702)64:2<278::AID-JCB11>3.0.CO
[4]
2-F
[5]
Isolation and characterization of Wharton's jelly-derived multipotent mesenchymal stromal cells obtained from bovine umbilical cord and maintained in a defined serum-free three-dimensional system [J].
Cardoso, Tereza C. ;
Ferrari, Heitor F. ;
Garcia, Andrea F. ;
Novais, Juliana B. ;
Silva-Frade, Camila ;
Ferrarezi, Marina C. ;
Andrade, Alexandre L. ;
Gameiro, Roberto .
BMC BIOTECHNOLOGY, 2012, 12
[6]
Comparison of Alternative Mesenchymal Stem Cell Sources for Cell Banking and Musculoskeletal Advanced Therapies [J].
Cavallo, Carola ;
Cuomo, Carmela ;
Fantini, Sara ;
Ricci, Francesca ;
Tazzari, Pier Luigi ;
Lucarelli, Enrico ;
Donati, Davide ;
Facchini, Andrea ;
Lisignoli, Gina ;
Fornasari, Pier Maria ;
Grigolo, Brunella ;
Moroni, Lorenzo .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2011, 112 (05) :1418-1430
[7]
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
[8]
Human fetal mesenchymal stem cells as vehicles for gene delivery [J].
Chan, J ;
O'Donoghue, K ;
De la Fuente, J ;
Roberts, IA ;
Kumar, S ;
Morgan, JE ;
Fisk, NM .
STEM CELLS, 2005, 23 (01) :93-102
[9]
Immunomodulatory properties of human adult and fetal multipotent mesenchymal stem cells [J].
Chen, Pei-Min ;
Yen, Men-Luh ;
Liu, Ko-Jiunn ;
Sytwu, Huey-Kang ;
Yen, B-Linju .
JOURNAL OF BIOMEDICAL SCIENCE, 2011, 18
[10]
Kinetics of the Cell Biological Changes Occurring in the Progression of DNA Damage-Induced Senescence [J].
Cho, Sohee ;
Park, Jihoon ;
Hwang, Eun Seong .
MOLECULES AND CELLS, 2011, 31 (06) :539-546