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A specific amyloid-β protein assembly in the brain impairs memory

14 July 2022 Editor’s Note: The editors of Nature have been alerted to concerns regarding some of the figures in this paper. Nature is investigating these concerns, and a further editorial response will follow as soon as possible. In the meantime, readers are advised to use caution when using results reported therein.

Abstract

Memory function often declines with age1, and is believed to deteriorate initially because of changes in synaptic function rather than loss of neurons2. Some individuals then go on to develop Alzheimer's disease with neurodegeneration. Here we use Tg2576 mice, which express a human amyloid-β precursor protein (APP) variant linked to Alzheimer's disease, to investigate the cause of memory decline in the absence of neurodegeneration or amyloid-β protein amyloidosis. Young Tg2576 mice (< 6 months old) have normal memory and lack neuropathology, middle-aged mice (6–14 months old) develop memory deficits without neuronal loss, and old mice (> 14 months old) form abundant neuritic plaques containing amyloid-β (refs 3–6). We found that memory deficits in middle-aged Tg2576 mice are caused by the extracellular accumulation of a 56-kDa soluble amyloid-β assembly, which we term Aβ*56 (Aβ star 56). Aβ*56 purified from the brains of impaired Tg2576 mice disrupts memory when administered to young rats. We propose that Aβ*56 impairs memory independently of plaques or neuronal loss, and may contribute to cognitive deficits associated with Alzheimer's disease.

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Figure 1: Temporal patterns of soluble Aβ oligomers and memory decline in Tg2576 mice.
Figure 2: Biochemical properties of Aβ assemblies in Tg2576 mice.
Figure 3: Levels of the 56-kDa Aβ assembly show the strongest inverse correlation with spatial memory.
Figure 4: Purification of Aβ*56 from Tg2576 brain and effects of purified Aβ*56 on memory in young rats.

Change history

  • 14 July 2022

    Editor’s Note: The editors of Nature have been alerted to concerns regarding some of the figures in this paper. Nature is investigating these concerns, and a further editorial response will follow as soon as possible. In the meantime, readers are advised to use caution when using results reported therein.

References

  1. Craik, F. I. in Handbook of the Psychology of Aging (eds Birren, J. E. & Schall, K.) 384–420 (Van Nostrand-Reinhold, New York, 1977)

    Google Scholar 

  2. Morrison, J. H. & Hof, P. R. Life and death of neurons in the aging brain. Science 278, 412–419 (1997)

    ADS  CAS  Article  Google Scholar 

  3. Hsiao, K. et al. Correlative memory deficits, Aβ elevation, and amyloid plaques in transgenic mice. Science 274, 99–102 (1996)

    ADS  CAS  Article  Google Scholar 

  4. Irizarry, M. C., McNamara, M., Fedorchak, K., Hsiao, K. & Hyman, B. T. APPSW transgenic mice develop age-related Aβ deposits and neuropil abnormalities, but no neuronal loss in CA1. J. Neuropathol. Exp. Neurol. 56, 965–973 (1997)

    CAS  Article  Google Scholar 

  5. Kawarabayashi, T. et al. Age-dependent changes in brain, CSF, and plasma amyloid β protein in the Tg2576 transgenic mouse model of Alzheimer's disease. J. Neurosci. 21, 372–381 (2001)

    CAS  Article  Google Scholar 

  6. Westerman, M. A. et al. The relationship between Aβ and memory in the Tg2576 mouse model of Alzheimer's disease. J. Neurosci. 22, 1858–1867 (2002)

    CAS  Article  Google Scholar 

  7. Kawas, C. H. et al. Visual memory predicts Alzheimer's disease more than a decade before diagnosis. Neurology 60, 1089–1093 (2003)

    CAS  Article  Google Scholar 

  8. Small, G. W. et al. Cerebral metabolic and cognitive decline in persons at genetic risk for Alzheimer's disease. Proc. Natl Acad. Sci. USA 97, 6037–6042 (2000)

    ADS  CAS  Article  Google Scholar 

  9. Bookheimer, S. Y. et al. Patterns of brain activation in people at risk for Alzheimer's disease. N. Engl. J. Med. 343, 450–456 (2000)

    CAS  Article  Google Scholar 

  10. Albert, M. S. Memory decline: the boundary between aging and age-related disease. Ann. Neurol. 51, 282–284 (2002)

    PubMed  Google Scholar 

  11. Benzing, W. C. et al. Evidence for glial-mediated inflammation in aged APPSW transgenic mice. Neurobiol. Aging 20, 581–589 (1999)

    CAS  Article  Google Scholar 

  12. Janus, C. et al. Aβ peptide immunization reduces behavioural impairment and plaques in a model of Alzheimer's disease. Nature 408, 979–982 (2000)

    ADS  CAS  Article  Google Scholar 

  13. Chen, G. et al. A learning deficit related to age and β-amyloid plaques in a mouse model of Alzheimer's disease. Nature 408, 975–979 (2000)

    ADS  CAS  Article  Google Scholar 

  14. Hsia, A. Y. et al. Plaque-independent disruption of neural circuits in Alzheimer's disease mouse models. Proc. Natl Acad. Sci. USA 96, 3228–3233 (1999)

    ADS  CAS  Article  Google Scholar 

  15. Klein, W. L., Krafft, G. A. & Finch, C. E. Targeting small Aβ oligomers: the solution to an Alzheimer's disease conundrum? Trends Neurosci. 24, 219–224 (2001)

    CAS  Article  Google Scholar 

  16. Ashe, K. H. Learning and memory in transgenic mice modeling Alzheimer's disease. Learn. Mem. 8, 301–308 (2001)

    CAS  Article  Google Scholar 

  17. Gordon, J. A. & Warren, J. R. Denaturation of globular proteins. I. The interaction of urea and thiourea with bovine plasma albumin. J. Biol. Chem. 243, 5663–5669 (1968)

    CAS  Article  Google Scholar 

  18. Kayed, R. et al. Common structure of soluble amyloid oligomers implies common mechanism of pathogenesis. Science 300, 486–489 (2003)

    ADS  CAS  Article  Google Scholar 

  19. Stern, E. A. et al. Cortical synaptic integration in vivo is disrupted by amyloid-β plaques. J. Neurosci. 24, 4535–4540 (2004)

    CAS  Article  Google Scholar 

  20. Billings, L. M., Oddo, S., Green, K. N., McGaugh, J. L. & Laferla, F. M. Intraneuronal Aβ causes the onset of early Alzheimer's disease-related cognitive deficits in transgenic mice. Neuron 45, 675–688 (2005)

    CAS  Article  Google Scholar 

  21. Orr, H. T. Neurodegenerative disease: neuron protection agency. Nature 431, 747–748 (2004)

    ADS  CAS  Article  Google Scholar 

  22. SantaCruz, K. et al. Tau suppression in a neurodegenerative mouse model improves memory function. Science 309, 476–481 (2005)

    ADS  CAS  Article  Google Scholar 

  23. Duff, K. & Planel, E. Untangling memory deficits. Nature Med. 11, 826–827 (2005)

    CAS  Article  Google Scholar 

  24. Gallagher, M., Burwell, R. & Burchinal, M. Severity of spatial learning impairment in aging: development of a learning index for performance in the Morris water maze. Behav. Neurosci. 107, 618–626 (1993)

    CAS  Article  Google Scholar 

  25. Walsh, D. M. et al. Naturally secreted oligomers of amyloid β protein potently inhibit hippocampal long-term potentiation in vivo. Nature 416, 535–539 (2002)

    ADS  CAS  Article  Google Scholar 

  26. Haass, C., Koo, E. H., Mellon, A., Hung, A. Y. & Selkoe, D. J. Targeting of cell-surface β-amyloid precursor protein to lysosomes: alternative processing into amyloid-bearing fragments. Nature 357, 500–503 (1992)

    ADS  CAS  Article  Google Scholar 

  27. Barelli, H. et al. Characterization of new polyclonal antibodies specific for 40 and 42 amino acid-long amyloid β peptides: their use to examine the cell biology of presenilins and the immunohistochemistry of sporadic Alzheimer's disease and cerebral amyloid angiopathy cases. Mol. Med. 3, 695–707 (1997)

    CAS  Article  Google Scholar 

  28. Sergeant, N. et al. Progressive decrease of amyloid precursor protein carboxy terminal fragments (APP-CTFs), associated with tau pathology stages, in Alzheimer's disease. J. Neurochem. 81, 663–672 (2002)

    CAS  Article  Google Scholar 

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Acknowledgements

We thank S. Younkin, D. Walsh, M. Podlisny, D. Selkoe, J. Cleary and S. Prusiner for critical discussions. We are grateful to D. Cooper-Blacketer, J. McQuail and M. Sherman for technical help, and A. Delacourte and N. Sergeant for providing the APPC17-Cter antiserum. This work was supported by grants from the NIH (to K.H.A., M.G. and A.Y.) and a gift from M. and H. Hobbs to M.G. Author Contributions S.L. and K.H.A. conceived the project. S.L. planned, performed and analysed the biochemistry experiments, including the protein extractions and purification of Aβ*56. K.H.A. wrote most of the paper. M.T.K. and M.G. planned, performed and analysed the rat behavioural experiments, and L.K. planned and analysed the mouse behavioural experiments. A.Y. provided the mass spectrometry analysis of purified Aβ*56, C.G.G. provided biochemistry advice, and C.G.G. and R.K. donated the A11 antiserum.

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Correspondence to Karen H. Ashe.

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S.L. and K.H.A. are inventors on a patent application submitted by the University of Minnesota that describes Aβ*56.

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Supplementary Notes

This file contains the Supplementary Methods, Supplementary Discussion (on the selective effects of Aβ*56 on retention, but not acquisition of spatial memory) Supplementary Table 1, Supplementary Figures 1–7 and additional references. (PDF 2010 kb)

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Lesné, S., Koh, M., Kotilinek, L. et al. A specific amyloid-β protein assembly in the brain impairs memory. Nature 440, 352–357 (2006). https://doi.org/10.1038/nature04533

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