Human adult stem cells hold promise for regenerative medicine. They are usually expanded for multiple passages to increase cell yield prior to transplantation. Unfortunately, prolonged culture leads to cell senescence, a major drawback from successful outcomes in cell therapy approaches. Here, we show that an extract from early Zebrafish embryo (ZF1) counteracted senescence progression in human adipose-derived stem cells (hASCs) along multiple culture passages (from the 5th to the 20th). Exposure to ZF1 strongly reduced the expression of senescence marker beta-galactosidase. Both stemness (, , and ) and anti-senescence (, and telomerase reverse transcriptase - ) related genes were overexpressed at specific experimental points, without recruitment of the cyclin-dependent kinase Inhibitor 2A (, ali-as ). Increased telomerase activity was associatt-ed with overexpression. Both osteogenic and adipogenic abilities were enhanced. In conclusion, hASCs exposure to ZF1 is a feasible tool to counteract and reverse human stem cell senescence in long-term culturing conditions.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.2741/S528 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!