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Un
                                                                      answered

                                                                      questions

                     Aβ Oligomers                                     &
                              Hilal A. Lashuel

                                                                      Un
            Swiss Federal Institute of Technology-Lausanne
                          Brain Mind Institute
  Laboratory of Molecular and Chemical Biology of Neurodegeneration   questioned

                                                                      answers
http://lashuel-lab.epfl.ch/
Unanswered Questions


•   What is the relationship between the different oligomeric forms of Aβ, which
    are on- and off-pathway and does it matter?

•   Are all dimers, trimers, dodecamers the same?

•   Does the size of the oligomer matter if we can’t measure it accurately?

•   Can we correlate size and structure to toxicity if the structure and aggregation
    states of the oligomers are dynamic and changing during the time of the
    experiment?

•   Could the difference in activity between synthetic and cell-derived oligomers
    be simply due to the kinetic stability of the oligomers formed in these
    preparations, SDS-Dimer are more stable?
     –   Can we compare synthetic, secreted or brain-derived oligomers if these samples are characterized
         by different level of complexity and molecular environments.




                                                                             H. Lashuel, http://lashuel-lab.epfl.ch/
Unquestioned answers
•   Natural Oligomers: How natural are natural oligomers?
    Cell-derived, Brain-derived Oligomers.

•   SDS-Stable oligomers: Why are these oligomers so stable?
    Are these species “covalently linked oligomers”?
    To what extent do covalent oligomers (e.g. disulfide-linked) oligomers mimic “natural oligomers”?


•   SDS-Stable Oligomers are the building block of amyloid fibrils in vivo and are
    the early mediators of neuronal dysfunction.

•   Quaternary structure and Conformational antibodies: Is it possible to develop
    conformational and species (dimer or trimer) specific antibodies using heterogeneous
    and unstable mixtures of oligomers as antigens?
    e.g. ADDLS are dodecamers???

•   Some oligomer species are more relevant to AD pathogenesis than others…
    What is the evidence that one oligomeric species is more toxic or correlate with
    disease progression than other?      LACK of comparative studies. WHY?
     – Synthetic vs. Natural
     – Dimers vs. Trimers, Aβ*56, ADDLS or Protofibrils
•   Several inhibitors of Aβ fibrillization act by stabilizing oligomeric forms of Aβ,
    yet these molecules protect against Aβ toxicity.
                                                                           H. Lashuel, http://lashuel-lab.epfl.ch/
What about the Process of fibrillization?


                                             Wogulis M. et al
                                             J Neurosci, 2005




                                                 Jan A. et al
                                            J. Biol. Chem, 2010




                                                 Jan A. et al
                                            J. Biol. Chem, 2008




                                            Kuperstein I. et al
                                            EMBO Journ, 2010


                                    H. Lashuel, http://lashuel-lab.epfl.ch/
What can we improve?
•   It is not always about Aβ

•   Self-criticism

•   Honest and open discussion and debate about data
    (communicate and negative results)

•   More Comparative studies

•   Sharing and exchange of reagents

•   Consensus on expreimental standards and terminology

•   More collaborations (interdisciplinary), especially to tackle very difficult and
    technically challenging questions.

•   Develop better Tools: Proactive recruitment and collaboration of experts from other
    fields

•   Private Foundations and Funding Agencies could play a more active role to
    foster and facilitate these interactions.
                                                                       H. Lashuel, http://lashuel-lab.epfl.ch/

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Alzforum webinar h lashuel

  • 1. Un answered questions Aβ Oligomers & Hilal A. Lashuel Un Swiss Federal Institute of Technology-Lausanne Brain Mind Institute Laboratory of Molecular and Chemical Biology of Neurodegeneration questioned answers http://lashuel-lab.epfl.ch/
  • 2. Unanswered Questions • What is the relationship between the different oligomeric forms of Aβ, which are on- and off-pathway and does it matter? • Are all dimers, trimers, dodecamers the same? • Does the size of the oligomer matter if we can’t measure it accurately? • Can we correlate size and structure to toxicity if the structure and aggregation states of the oligomers are dynamic and changing during the time of the experiment? • Could the difference in activity between synthetic and cell-derived oligomers be simply due to the kinetic stability of the oligomers formed in these preparations, SDS-Dimer are more stable? – Can we compare synthetic, secreted or brain-derived oligomers if these samples are characterized by different level of complexity and molecular environments. H. Lashuel, http://lashuel-lab.epfl.ch/
  • 3. Unquestioned answers • Natural Oligomers: How natural are natural oligomers? Cell-derived, Brain-derived Oligomers. • SDS-Stable oligomers: Why are these oligomers so stable? Are these species “covalently linked oligomers”? To what extent do covalent oligomers (e.g. disulfide-linked) oligomers mimic “natural oligomers”? • SDS-Stable Oligomers are the building block of amyloid fibrils in vivo and are the early mediators of neuronal dysfunction. • Quaternary structure and Conformational antibodies: Is it possible to develop conformational and species (dimer or trimer) specific antibodies using heterogeneous and unstable mixtures of oligomers as antigens? e.g. ADDLS are dodecamers??? • Some oligomer species are more relevant to AD pathogenesis than others… What is the evidence that one oligomeric species is more toxic or correlate with disease progression than other? LACK of comparative studies. WHY? – Synthetic vs. Natural – Dimers vs. Trimers, Aβ*56, ADDLS or Protofibrils • Several inhibitors of Aβ fibrillization act by stabilizing oligomeric forms of Aβ, yet these molecules protect against Aβ toxicity. H. Lashuel, http://lashuel-lab.epfl.ch/
  • 4. What about the Process of fibrillization? Wogulis M. et al J Neurosci, 2005 Jan A. et al J. Biol. Chem, 2010 Jan A. et al J. Biol. Chem, 2008 Kuperstein I. et al EMBO Journ, 2010 H. Lashuel, http://lashuel-lab.epfl.ch/
  • 5. What can we improve? • It is not always about Aβ • Self-criticism • Honest and open discussion and debate about data (communicate and negative results) • More Comparative studies • Sharing and exchange of reagents • Consensus on expreimental standards and terminology • More collaborations (interdisciplinary), especially to tackle very difficult and technically challenging questions. • Develop better Tools: Proactive recruitment and collaboration of experts from other fields • Private Foundations and Funding Agencies could play a more active role to foster and facilitate these interactions. H. Lashuel, http://lashuel-lab.epfl.ch/