RESUMEN
In recent years, tissue regeneration has become a promising field for developing stem cellbased transplantation therapies for human patients. Adult stem cells are affected by the same aging mechanisms that involve somatic cells. One of the mechanisms involved in cellular aging is hyperactivation of mechanistic target of rapamycin complex 1 [mTORC1] and disruption of 50 adenosine monophosphate-activated protein kinase [AMPK]. Aging of stem cells results in their
impaired regenerative capacity and depletion of stem cell pools in adult tissue, which results in lower efficacy of stem cell therapy. By utilizing an effective therapeutic intervention for aged stem cells, stem cell therapy can become more promising for future application. mTORC1 inhibition is a practical approach to preserve the stem cell pool. In this article, we review the dynamic interaction between sirtuin [silent mating type information regulation 2 homolog] 1, AMPK, and mTORC1. We propose that using AMPK activators such as 5-aminoimidazole-4- carboxamide ribonucleotide, A769662, metformin, and oxidized nicotinamide adenine dinucleotide [NAD+] are practical ways to be employed for achieving better optimized results in stem cell-based transplantation therapies