The Influence of Aging on the Regenerative Potential of Human Adipose Derived Mesenchymal Stem Cells
Monika Marędziak , Krzysztof Marycz , Krzysztof A. Tomaszewski , Katarzyna Kornicka , Brandon Michael Henry
AbstractTissue 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.
|Journal series||Stem Cells International, ISSN 1687-966X, (A 20 pkt)|
|Publication size in sheets||0.7|
|Score|| = 20.0, 10-05-2021, ArticleFromJournal|
= 20.0, 10-05-2021, ArticleFromJournal
|Publication indicators||= 91; = 118; : 2016 = 0.899; : 2016 = 3.54 (2) - 2016=3.39 (5)|
|Citation count*||156 (2021-06-08)|
* presented citation count is obtained through Internet information analysis and it is close to the number calculated by the Publish or Perish system.