For decades researches have been investigating the underlying foundations of Alzheimer’s disease to provide clues for the design of a successful therapy. This week, UK DRI Director Bart De Strooper and colleagues at VIB/KU Leuven have published breakthrough insights in the prestigious journal Cell.
A collaboration between Professor Lucía Chávez-Gutiérrez and Professor Bart De Strooper revealed the molecular basis of the hereditary form of Alzheimer’s disease that strikes early in life. These new findings provide powerful insights for the design of novel therapeutic strategies to tackle the disease.
This work provides a unifying hypothesis that explains how mutations in the two major genes for Alzheimer's disease act on a similar fundamental mechanism.Professor Bart De StrooperUK DRI Director
The hereditary form of Alzheimer’s disease is caused by mutations in the Gamma Secretase enzyme and the APP protein. Gamma Secretase cuts APP several times in a progressive manner, with each cleavage generating a shorter fragment, called amyloid beta, which gets released into the brain.
The research team discovered that disease-causing mutations in Gamma secretase and APP disrupt the cleavage process leading to the generation of longer amyloid beta fragments that are only partially digested. These longer amyloid fragments are thought to cause widespread neuronal death, resulting in memory problems and other symptoms of Alzheimer’s disease, before aggregating into amyloid plaques (a hallmark of the disease).
The researchers uncovered that the disease-causing mutations disrupt this process by weakening the interactions of Gamma Secretase and APP during the progressive cleavages. In that way they promote the premature release of longer amyloid beta fragments. The more the Gamma Secretase-APP interaction is undermined, the sooner Alzheimer's disease develops. The report also suggests that changes in the cellular environment could modulate the interaction between Gamma secretase and APP, and could therefore also affect someone’s risk to develop the non-hereditary form of Alzheimer’s disease.
These findings have important implications for the prevention or treatment of the disease. Previous attempts to tackle the toxic effects of amyloid beta have mostly focused on blocking its production or removing the amyloid plaques from the brain. However, the new insights suggest that stabilizing the interaction between Gamma secretase and APP might be sufficient to avoid the release of longer and toxic amyloid beta fragments and in that way prevent or delay the disease.
The team will collaborate with academic drug discovery units to translate these new findings to new therapeutic drug candidates.
This deep insight into one of the causes of Alzheimer's disease has also yielded a novel drug screening assay which is now exploited by the Drug Discovery Centre at UCL.Professor Bart De StrooperUK DRI Director
Szaruga et al. Destabilized γ-Secretase-Aβn interactions cause Alzheimer’s disease. Cell 2017
In collaboration with researchers from Mannheim University, Janssen Pharmaceutica, RIKEN Brian Science Institute and University College London and the VIB Core Facilities.