The Influence of Aging on the Regenerative Potential of Human Adipose Derived Mesenchymal Stem Cells

被引:181
作者
Maredziak, Monika [1 ,2 ]
Marycz, Krzysztof [2 ,3 ]
Tomaszewski, Krzysztof A. [4 ]
Kornicka, Katarzyna [2 ]
Henry, Brandon Michael [4 ]
机构
[1] Wroclaw Univ Environm & Life Sci, Dept Anim Physiol & Biostruct, Fac Vet Med, PL-50375 Wroclaw, Poland
[2] Wroclaw Univ Environm & Life Sci, Electron Microscopy Lab, PL-50631 Wroclaw, Poland
[3] Wroclaw Res Ctr EIT, PL-54066 Wroclaw, Poland
[4] Jagiellonian Univ, Dept Anat, Coll Med, PL-31034 Krakow, Poland
关键词
HUMAN BONE-MARROW; IN-VITRO; DEGENERATIVE ARTHRITIS; PROGENITOR CELLS; STROMAL CELLS; DIFFERENTIATION; TISSUE; AGE; OSTEOARTHRITIS; SENESCENCE;
D O I
10.1155/2016/2152435
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Tissue regeneration using human adipose derived mesenchymal stem cells (hASCs) has significant potential as a novel treatment for many degenerative bone and joint diseases. Previous studies have established that age negatively affects the proliferation status and the osteogenic and chondrogenic differentiation potential of mesenchymal stem cells. The aim of this study was to assess the age-related maintenance of physiological function and differentiation potential of hASCs in vitro. hASCs were isolated from patients of four different age groups: (1) > 20 years (n = 7), (2) > 50 years (n = 7), (3) > 60 years (n = 7), and (4) > 70 years (n = 7). The hASCs were characterized according to the number of fibroblasts colony forming unit (CFU-F), proliferation rate, population doubling time (PDT), and quantified parameters of adipogenic, chondrogenic, and osteogenic differentiation. Compared to younger cells, aged hASCs had decreased proliferation rates, decreased chondrogenic and osteogenic potential, and increased senescent features. A shift in favor of adipogenic differentiation with increased age was also observed. As many bone and joint diseases increase in prevalence with age, it is important to consider the negative influence of age on hASCs viability, proliferation status, and multilineage differentiation potential when considering the potential therapeutic applications of hASCs.
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页数:15
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