‘It is essential to carefully characterize and classify the mechanisms that underlie Alzheimer’s disease, in order to allow for the development of novel therapies that can be prescribed according to the patient’s relevant disease sub-type.’
Deciphering the mechanism that underlies the development of Alzheimer’s disease in certain families but not in others, researchers at the Hebrew University of Jerusalem’s Faculty of Medicine have proposed that the malady is actually a collection of diseases that probably should be treated with a variety of different approaches.
Neurodegenerative diseases are incurable and debilitating conditions that result in degeneration or death of cells in the nervous system. Conditions such as prion disorders (the most famous of which is “Mad Cow Disease”), Alzheimer’s Disease and Parkinson’s Disease share two key features: they emerge as a result of aberrant protein folding and aggregation, and their onset is late in life. These maladies emerge either sporadically or as familial, mutation-linked illnesses (certain prion disease can be also infectious).
Most sporadic cases are diagnosed during the patient’s seventh decade of life or later, while familial cases typically manifest during the fifth or sixth decade. Despite their relative rareness, mutation-linked cases are very important, as they provide hints that can help decipher the mechanisms that underlie the development of the disease.
The late onset feature typical to distinct neurodegenerative diseases, and the common temporal emergence patterns of these maladies, raise key questions: first, why do individuals who carry disease-linked mutation show no clinical signs until their fifth or sixth decade of life? In addition, why do apparently distinct disorders share a common temporal emergence pattern?
One possible explanation is that as people age, the efficiency of the mechanisms that protect younger people from the toxic aggregation of proteins declines, thus exposing them to disease. Indeed, previous studies clearly indicate that the aging process plays key roles in enabling neurodegenerative disorders to onset late in life.
These finding raised the question of what mechanisms are negatively regulated by aging, allowing the emergence of neurodegeneration in the elderly.
Since neurodegenerative disorders stem from aberrant protein folding, an international research team, led by Prof. Ehud Cohen and Dr. Tziona Ben-Gedalya at The Institute for Medical Research Israel – Canada (IMRIC) in the Hebrew University’s Faculty of Medicine, postulated that an aging-associated decline in the activity of proteins that assist other proteins to fold properly, may be one mechanism that exposes the elderly to neurodegeneration.
To identify such mechanisms, they searched for similar mutational patterns in different proteins that are linked to the development of distinct neurodegenerative disorders. Their research showed that the development of Alzheimer’s disease in certain families, and of a familial prion disorder in other families, originate from very similar mutational patterns.
Based on this discovery, they identified that the malfunction of the protein “cyclophilin B,” which helps nascent proteins to attain their proper spatial structures, is responsible for the manifestation of both maladies. They also comprehensively characterized the mechanism that underlies the development of Alzheimer’s disease in individuals who carry these mutations, and found that it has no relevance to the emergence of the disease in patients who carry other Alzheimer’s-linked mutations.
According to Prof. Ehud Cohen: “This study provides important new insights: first, it shows that the development of distinct neurodegenerative disorders stems from a similar mechanism. More importantly, it indicates that Alzheimer’s disease can emanate from more than one mechanism, suggesting that it is actually a collection of diseases that should be classified.”
The new insights derived from this study may reinforce the efforts to develop novel therapies to the different subtypes of Alzheimer’s disease, providing new hope to those who suffer from this incurable disorder and to their families.
Prof. Ehud Cohen added: “Our study proposes that the failure to develop efficient Alzheimer’s therapy emanates from the pooling, in clinical experiments, of patients who suffer from distinct disorders that eventually lead to Alzheimer’s symptoms. Therefore it is essential to carefully characterize and classify the mechanisms that underlie Alzheimer’s disease, in order to allow for the development of novel therapies that can be prescribed to the individual patient according to their relevant disease subtype.”
The paper’s co-authors include researchers at the Institute for Dental Sciences, Faculty of Dental Medicine, Hebrew University of Jerusalem; Dept. of Physiology and Pharmacology at the Sackler Faculty of Medicine at Tel Aviv University; Dept. of Biochemistry and Molecular Biology, Wise Faculty of Life Sciences, Tel Aviv University; and Bone and Extracellular Matrix Branch, NICHD, National Institutes of Health (NIH), USA.
Funding: The study was supported by the Rosalinde and Arthur Gilbert Foundation (AFAR), the European Research Council, the National Institute for Psychobiology in Israel (NIPI), and the Israel Science Foundation.
Source: Dov Smith – Hebrew University of Jerusalem
Image Source: The image is in the public domain
Original Research: Abstract for “Alzheimer’s disease‐causing proline substitutions lead to presenilin 1 aggregation and malfunction” by Tziona Ben‐Gedalya, Lorna Moll, Michal Bejerano‐Sagie, Samuel Frere, Wayne A Cabral, Dinorah Friedmann‐Morvinski, Inna Slutsky, Tal Burstyn‐Cohen, Joan C Marini, and Ehud Cohen in EMBO Journal. Published online October 5 2015 doi:10.15252/embj.201592042
Alzheimer’s disease‐causing proline substitutions lead to presenilin 1 aggregation and malfunction
Do different neurodegenerative maladies emanate from the failure of a mutual protein folding mechanism? We have addressed this question by comparing mutational patterns that are linked to the manifestation of distinct neurodegenerative disorders and identified similar neurodegeneration‐linked proline substitutions in the prion protein and in presenilin 1 that underlie the development of a prion disorder and of familial Alzheimer’s disease (fAD), respectively. These substitutions were found to prevent the endoplasmic reticulum (ER)‐resident chaperone, cyclophilin B, from assisting presenilin 1 to fold properly, leading to its aggregation, deposition in the ER, reduction of γ‐secretase activity, and impaired mitochondrial distribution and function. Similarly, reduced quantities of the processed, active presenilin 1 were observed in brains of cyclophilin B knockout mice. These discoveries imply that reduced cyclophilin activity contributes to the development of distinct neurodegenerative disorders, propose a novel mechanism for the development of certain fAD cases, and support the emerging theme that this disorder can stem from aberrant presenilin 1 function. This study also points at ER chaperones as targets for the development of counter‐neurodegeneration therapies.
“Alzheimer’s disease‐causing proline substitutions lead to presenilin 1 aggregation and malfunction” by Tziona Ben‐Gedalya, Lorna Moll, Michal Bejerano‐Sagie, Samuel Frere, Wayne A Cabral, Dinorah Friedmann‐Morvinski, Inna Slutsky, Tal Burstyn‐Cohen, Joan C Marini, and Ehud Cohen in EMBO Journal. Published online October 5 2015 doi:10.15252/embj.201592042