Donor age negatively impacts adipose tissue-derived mesenchymal stem cell expansion and differentiation

被引:368
作者
Choudhery, Mahmood S. [1 ,2 ]
Badowski, Michael [2 ]
Muise, Angela [2 ]
Pierce, John [3 ]
Harris, David T. [2 ]
机构
[1] King Edward Med Univ, Adv Ctr Res Biomed Sci, Lahore, Pakistan
[2] Univ Arizona, Coll Med, Dept Immunobiol, Tucson, AZ 85724 USA
[3] Aesthet Surg Tucson, Tucson, AZ USA
来源
JOURNAL OF TRANSLATIONAL MEDICINE | 2014年 / 12卷
关键词
Adipose tissue; Mesenchymal stem cells; Donor age; Regenerative potential; Growth kinetics; In vitro differentiation potential; BONE-MARROW; STROMAL CELLS; IN-VITRO; THERAPIES; DISEASE; PROLIFERATION; ANGIOGENESIS; SENESCENCE; CULTURE; GROWTH;
D O I
10.1186/1479-5876-12-8
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Human adipose tissue is an ideal autologous source of mesenchymal stem cells (MSCs) for various regenerative medicine and tissue engineering strategies. Aged patients are one of the primary target populations for many promising applications. It has long been known that advanced age is negatively correlated with an organism's reparative and regenerative potential, but little and conflicting information is available about the effects of age on the quality of human adipose tissue derived MSCs (hAT-MSCs). Methods: To study the influence of age, the expansion and in vitro differentiation potential of hAT-MSCs from young (<30 years), adult (35-50 years) and aged (>60 years) individuals were investigated. MSCs were characterized for expression of the genes p16(INK4a) and p21 along with measurements of population doublings (PD), superoxide dismutase (SOD) activity, cellular senescence and differentiation potential. Results: Aged MSCs displayed senescent features when compared with cells isolated from young donors, concomitant with reduced viability and proliferation. These features were also associated with significantly reduced differentiation potential in aged MSCs compared to young MSCs. Conclusions: In conclusion, advancing age negatively impacts stem cell function and such age related alterations may be detrimental for successful stem cell therapies.
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页数:14
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