4.6 Article

Morphological, molecular and functional differences of adult bone marrow- and adipose-derived stem cells isolated from rats of different ages

Journal

EXPERIMENTAL CELL RESEARCH
Volume 318, Issue 16, Pages 2034-2048

Publisher

ELSEVIER INC
DOI: 10.1016/j.yexcr.2012.05.008

Keywords

Strol; Notch; p53; p38; Mitochondria; Senescence; Aging

Funding

  1. Rosetrees Trust
  2. Swedish Medical Research Council, (EU)
  3. County of Vasterbotten
  4. Aner Foundation
  5. British Council/CRUI (British-Italian Partnership Programme for Young Researchers)
  6. Regione Piemonte (Progetto Ricerca Sanitaria Finalizzata)

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Adult mesenchymal stem cells have self-renewal and multiple differentiation potentials, and play important roles in regenerative medicine. However, their use may be limited by senescence or age of the donor, leading to changes in stem cell functionality. We investigated morphological, molecular and functional differences between bone marrow-derived (MSC) and adipose-derived (ASC) stem cells isolated from neonatal, young and old rats compared to Schwann cells from the same animals. Immunocytochemistry, RT-PCR, proliferation assays, western blotting and transmission electron microscopy were used to investigate expression of senescence markers. Undifferentiated and differentiated ASC and MSC from animals of different ages expressed Notch-2 at similar levels; protein-38 and protein-53 were present in all groups of cells with a trend towards increased levels in cells from older animals compared to those from neonatal and young rats. Following co-culture with adult neuronal cells, dMSC and dASC from animals of all ages elicited robust neurite outgrowth. Mitotracker (R) staining was consistent with ultrastructural changes seen in the mitochondria of cells from old rats, indicative of senescence. In conclusion, this study showed that although the cells from aged animals expressed markers of senescence, aged MSC and ASC differentiated into SC-like cells still retain potential to support axon regeneration. Crown Copyright (C) 2012 Published by Elsevier Inc. All rights reserved.

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