DGIST’s research team have been conducting research to reverse the aging process by shifting the existing academia’s ‘irreversibility of aging’ paradigm that suggests aging cannot be reversed. To reverse aging, the research team searched for factors that could control aging and sought substances that could restore cell division capacity.
As a result, it was confirmed that KU-60019, an inhibitor of the ATM protein, which is a phosphorylation enzyme, restores the functions of aging cells through activation of lysosomal functions and induction of cell proliferation.
The degradation of lysosomes, which are intracellular organelles responsible for autophagy and decomposition of biopolymers such as proteins and lipids in the cell, leads to cell senescence by accumulating biomolecules that must be removed in cells and causes instability of the metabolism such as removal of dysfunctional mitochondria.
The research confirmed that as cell aging progresses, the vacuolar ATPase (v-ATPase) protein involved in the lysosomal activity regulation is phosphorylated by the ATM protein, and the binding force between the units constituting the v-ATPase is weakened, so consequently the function of lysosomes deteriorates. In addition, the team has proven that the reversible recovery of aging is possible.
They experimentally demonstrated that the regulation of ATM protein activation by KU-60019 substances induces the reduction of phosphorylation of v-ATPase, thereby inducing recovery of mitochondrial function and functional recovery of the lysosome and autophagy system as well as promoting wound healing in aging animal models.
DGIST Chair Professor Park SangChul said, "The significance and implication of this study is that it is possible to reverse the recovery of aging cells by inhibiting and restoring the degradation of lysosomal function. In the future, we will continue to conduct studies that extend the life expectancy of human beings by verifying and validating efficacy and safety through aging animal models."