My watch list
my.bionity.com  
Login  

Probiodrug Collaborators Explain Interplay of Key Suspects in Alzheimer’s Disease

Nature paper demonstrates that toxicity in AD is induced by pyroglutamate Abeta and is tau protein dependent

04-05-2012: Probiodrug AG announced its scientists and academics collaborators published seminal findings on the role of pyroglu Aβ in AD pathology in Nature. The new findings add to the growing body of evidence that pyroglu Aβ plays a crucial role in the initiation of AD. In addition, the research results further elucidate the mechanism by which pyroglu Aβ triggers neuronal toxicity.

The data published today suggest that pyroglu Aβ co-aggregates with “normal” Aβ peptides to form low molecular weight oligomers (LMOs), which are structurally distinct and far more toxic to cultured neurons than oligomers derived from normal Aβ. Moreover, the presence of the neuronal protein tau is essential for toxicity mediated by LMOs that contain pyroglu Aβ. The results have been substantiated in transgenic mice designed to express increased levels of pyroglu Aβ. In these animals, the pyroglu Aβ mediated neuronal loss and gliosis was prevented, if tau expression was shut down. The study is supplemented by results published in the Journal of Neurochemistry (online April 2012). Here the Probiodrug researchers reveal, that the aggregation propensity is caused by the hydrophobic nature of pyroglu Aβ.

The scientists also were able to demonstrate that the cytotoxicity is propagated by a prion-like templating mechanism of Aβ misfolding initiated by pyroglu Aβ: even after strong dilution to a solution containing only 0.000625% pyroglu Aβ, the mix after 24h developed enough toxicity to kill 50% of neurons treated with it.

“This publication delivers significant evidence to our hypothesis that pyroglu Aβ plays a critical role in the initiation of AD,” said Prof. Dr. Hans-Ulrich Demuth, CSO of Probiodrug. “It was also extremely surprising to us, that the pyroglu Aβ containing or propagated low-molecular weight oligomers remain stable for days - in contrast to the short-lived oligomers not formed by the pyroglu Aβ initiated mechanism. The new data for the first time demonstrate a relationship between pyroglu Aβ oligomer formation and tau protein in the development of neuronal toxicity.”

Original publication:
Nature 2012.

Contact / Request information

Request further information free of charge:

Watchlist

This is where you can add this news to your personal favourites

Additional Information

Facts, background information, dossiers
More about Probiodrug
  • News

    Evotec enters biology collaboration with Probiodrug

    Evotec AG announced that it has entered into a collaboration with Probiodrug AG. Under the terms of the agreement, Evotec will setup and validate assays to support the pre-clinical and clinical development of glutaminyl cyclase (QC) inhibitors for the treatment of Alzheimer's disease. Gluta ... more

    Probiodrug Collaborators Explain Interplay of Key Suspects in Alzheimer’s Disease

    Probiodrug AG announced its scientists and academics collaborators published seminal findings on the role of pyroglu Aβ in AD pathology in Nature. The new findings add to the growing body of evidence that pyroglu Aβ plays a crucial role in the initiation of AD. In addition, the research res ... more

    Probiodrug Further Expands Scientific Advisory Board by Appointing Prof Dr Dr hc Christian Haass

    Probiodrug AG announced the appointment of Prof Dr Dr hc Christian Haass to the Company's Scientific Advisory Board. In his work, Prof Haass focuses on the molecular and cellular mechanisms of Alzheimer's and Parkinson's disease. In Alzheimer's disease, he has elucidated the biochemistry an ... more

  • Companies

    Probiodrug AG

    Probiodrug is a biopharmaceutical company focused on the development of innovative small molecule drugs for the treatment of neuronal, inflammatory, and autoimmune diseases. In these areas, Probiodrug is focusing on innovative targets with the prospect of first and best in class therapeutic ... more

Your browser is not current. Microsoft Internet Explorer 6.0 does not support some functions on Chemie.DE