Researchers predicted that the main gene involved in inherited Alzheimer’s disease, PSEN1, would be important for supplying iron to brain cells.
University of Adelaide researchers have found important evidence supporting their theory that a deficiency of active iron in the brain is an important factor in Alzheimer’s disease.
Mutations in a small number of genes can cause an inherited form of Alzheimer’s disease that afflicts people when they are relatively young. Currently, the dominant theory of what causes Alzheimer’s disease is that these mutated genes change the way a small protein fragment, Amyloid beta, is produced. Many researchers believe that Amyloid beta can build up, become toxic, and eventually destroy brain function.
The new study – published in the Journal of Alzheimer’s Disease – follows the proposal of a group of Adelaide scientists and their collaborators who predicted that the main gene involved in inherited Alzheimer’s disease, PSEN1, would be important for supplying iron to brain cells.
“The active iron signal seems to clearly distinguish Alzheimer’s disease brains from other brains that had buildup of Amyloid beta but did not have memory problems,”Dr Michael Lardelli, School of Biological Sciences’ Alzheimer’s Disease Genetics Laboratory
Dr Michael Lardelli, from the University of Adelaide’s Alzheimer’s Disease Genetics Laboratory in the School of Biological Sciences, said: “Brain cells are a bit like people when it comes to getting the nutrition they need. Just as people have acid in their stomachs to help break down food, cells have microscopic acid-filled stomachs called ‘lysosomes’.
“If the lysosome is not acidic enough, the cell will have difficulty absorbing nutrients from outside. The cell will also have difficulty recycling materials it no longer needs in order to reuse them for other tasks. Research by others has shown that when the PSEN1 gene is mutated, cells’ lysosomes cannot become properly acidic.
“Iron is very, very important for cell survival. And it turns out that having sufficiently acidic lysosomes is very important for providing iron to cells. Without sufficient active iron, the cell’s powerhouses – its mitochondria – malfunction and cause damage. The mitochondria become a bit like microscopic nuclear powerplants that are leaking radioactivity.”
The team had to develop a new method for detecting evidence that the balance of active iron in brains was upset.
“Most of this was done by PhD. student, Nhi Hin, who won our university’s Doctoral Research Medal for her work, and her supervisor, Dr Stephen Pederson,” said Dr Lardelli.
“When we used the new technique to analyse the brain data we already had from our Alzheimer’s mutant fish, we could see clear evidence for the iron disturbance we had predicted. Nhi Hin then applied the same technique to data from the brains of people who had died with Alzheimer’s disease. There was a very strong signal there too. In fact, the active iron signal seems to clearly distinguish Alzheimer’s disease brains from other brains that had buildup of Amyloid beta but did not have memory problems.”
Dr Lardelli said the findings had implications for those at risk of developing Alzheimer’s disease.
“It has long been known that having sufficient iron in your diet is very important for mental function and overall health. But iron is both a blessing and a curse,” he said.
“Having too much iron can damage your body. So, people should not start taking iron supplements unless their doctor recommends they do so. In the meantime, we need more research to find a way to overcome the defective acidification problem of the lysosomes. That would likely solve the brain’s iron problem and other cell nutrition problems that may be contributing to Alzheimer’s disease.”
