Imagine the process of cleaning up a messy room. Now picture this scenario on a microscopic scale, where tiny proteins called α-synuclein accumulate and cause havoc in the brain cells of individuals with Parkinson’s disease (PD). Researchers have proposed a mathematical model to understand how these aggregated α-synuclein proteins are degraded by a cellular pathway called the autophagy lysosome pathway (ALP). They also explored the interplay between ALP and another signaling pathway called mTOR. Using bifurcation analysis, they discovered that α-synuclein can exist in three different states of stability under various stress conditions. Specifically, they found that under oxidative stress, the aggregation of α-synuclein can be reversed through ALP degradation pathways. Moreover, they investigated the role of mTOR in maintaining the dynamic features of these different states. This study opens up exciting opportunities for further experiments and simulations to delve deeper into the degradation mechanism of α-synuclein in PD.
Accumulation of the misfolded synaptic protein α-synuclein (αSyn*) is a hallmark of neurodegenerative disease in Parkinson’s disease (PD). Recent studies suggest that the autophagy lysosome pathway (ALP) including both the Beclin1-associated and mTOR-signaling pathways is involved in the αSyn* clearance mechanism. In this study, a mathematical model is proposed for the degradation of αSyn* by ALP with the crosstalk element of mTOR. Using codimension-1 bifurcation analysis, the tri-stability of αSyn* is surveyed under three different stress signals and, in addition, consideration is given to the regulatory mechanisms for the Beclin1- and mTOR-dependent rates on αSyn* degradation using the codimension-1 and−2 bifurcation diagrams. It was found that, especially under internal and external oxidative stresses (S1), the bistable switch of the aggregation of αSyn* can be transformed from an irreversible to a reversible condition through the ALP degradation pathways. Furthermore, the robustness of the tri-stable state for the stress S1 to the parameters related to mTOR-mediated ALP was probed. It was confirmed that mTOR-mediated ALP is important for maintaining the essential dynamic features of the tri-stable state. This study may provide a promising avenue for conducting further experiments and simulations of the degradation mechanism of dynamic modeling in PD.
Dr. David Lowemann, M.Sc, Ph.D., is a co-founder of the Institute for the Future of Human Potential, where he leads the charge in pioneering Self-Enhancement Science for the Success of Society. With a keen interest in exploring the untapped potential of the human mind, Dr. Lowemann has dedicated his career to pushing the boundaries of human capabilities and understanding.
Armed with a Master of Science degree and a Ph.D. in his field, Dr. Lowemann has consistently been at the forefront of research and innovation, delving into ways to optimize human performance, cognition, and overall well-being. His work at the Institute revolves around a profound commitment to harnessing cutting-edge science and technology to help individuals lead more fulfilling and intelligent lives.
Dr. Lowemann’s influence extends to the educational platform BetterSmarter.me, where he shares his insights, findings, and personal development strategies with a broader audience. His ongoing mission is shaping the way we perceive and leverage the vast capacities of the human mind, offering invaluable contributions to society’s overall success and collective well-being.
