Mechanism of Cellular Formation and In Vivo Seeding Effects of Hexameric β-Amyloid Assemblies.


Journal

Molecular neurobiology
ISSN: 1559-1182
Titre abrégé: Mol Neurobiol
Pays: United States
ID NLM: 8900963

Informations de publication

Date de publication:
Dec 2021
Historique:
received: 27 05 2021
accepted: 14 09 2021
pubmed: 6 10 2021
medline: 18 3 2022
entrez: 5 10 2021
Statut: ppublish

Résumé

The β-amyloid peptide (Aβ) is found as amyloid fibrils in senile plaques, a typical hallmark of Alzheimer's disease (AD). However, intermediate soluble oligomers of Aβ are now recognized as initiators of the pathogenic cascade leading to AD. Studies using recombinant Aβ have shown that hexameric Aβ in particular acts as a critical nucleus for Aβ self-assembly. We recently isolated hexameric Aβ assemblies from a cellular model, and demonstrated their ability to enhance Aβ aggregation in vitro. Here, we report the presence of similar hexameric-like Aβ assemblies across several cellular models, including neuronal-like cell lines. In order to better understand how they are produced in a cellular context, we investigated the role of presenilin-1 (PS1) and presenilin-2 (PS2) in their formation. PS1 and PS2 are the catalytic subunits of the γ-secretase complex that generates Aβ. Using CRISPR-Cas9 to knockdown each of the two presenilins in neuronal-like cell lines, we observed a direct link between the PS2-dependent processing pathway and the release of hexameric-like Aβ assemblies in extracellular vesicles. Further, we assessed the contribution of hexameric Aβ to the development of amyloid pathology. We report the early presence of hexameric-like Aβ assemblies in both transgenic mice brains exhibiting human Aβ pathology and in the cerebrospinal fluid of AD patients, suggesting hexameric Aβ as a potential early AD biomarker. Finally, cell-derived hexameric Aβ was found to seed other human Aβ forms, resulting in the aggravation of amyloid deposition in vivo and neuronal toxicity in vitro.

Identifiants

pubmed: 34608607
doi: 10.1007/s12035-021-02567-8
pii: 10.1007/s12035-021-02567-8
pmc: PMC8639606
doi:

Substances chimiques

Amyloid beta-Peptides 0
Presenilins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

6647-6669

Subventions

Organisme : Fonds De La Recherche Scientifique - FNRS
ID : PDRT.0177.18

Informations de copyright

© 2021. The Author(s).

Références

Haass C, Kaether C, Thinakaran G, Sisodia S (2012) Trafficking and proteolytic processing of APP. Cold Spring Harb Perspect Med 2(5):a006270. https://doi.org/10.1101/cshperspect.a006270
doi: 10.1101/cshperspect.a006270 pubmed: 22553493 pmcid: 3331683
Takami M, Nagashima Y, Sano Y, Ishihara S, Morishima-Kawashima M, Funamoto S, Ihara Y (2009) gamma-Secretase: successive tripeptide and tetrapeptide release from the transmembrane domain of beta-carboxyl terminal fragment. J Neurosci 29(41):13042–13052. https://doi.org/10.1523/jneurosci.2362-09.2009
doi: 10.1523/jneurosci.2362-09.2009 pubmed: 19828817 pmcid: 6665297
Bitan G, Kirkitadze MD, Lomakin A, Vollers SS, Benedek GB, Teplow DB (2003) Amyloid beta -protein (Abeta) assembly: Abeta 40 and Abeta 42 oligomerize through distinct pathways. Proc Natl Acad Sci USA 100(1):330–335. https://doi.org/10.1073/pnas.222681699
doi: 10.1073/pnas.222681699 pubmed: 12506200
Benilova I, Karran E, De Strooper B (2012) The toxic Aβ oligomer and Alzheimer’s disease: an emperor in need of clothes. Nat Neurosci 15(3):349–357. https://doi.org/10.1038/nn.3028
doi: 10.1038/nn.3028 pubmed: 22286176
Almeida ZL, Brito RMM (2020) Structure and aggregation mechanisms in amyloids. Molecules. https://doi.org/10.3390/molecules25051195
doi: 10.3390/molecules25051195 pubmed: 33287192 pmcid: 7730986
Sengupta U, Nilson AN, Kayed R (2016) The role of amyloid-β oligomers in toxicity, propagation, and immunotherapy. EBioMedicine 6:42–49. https://doi.org/10.1016/j.ebiom.2016.03.035
doi: 10.1016/j.ebiom.2016.03.035 pubmed: 27211547 pmcid: 4856795
Ye L, Fritschi SK, Schelle J, Obermüller U, Degenhardt K, Kaeser SA, Eisele YS, Walker LC, et al (2015) Persistence of Aβ seeds in APP null mouse brain. Nat Neurosci 18(11):1559–1561. https://doi.org/10.1038/nn.4117
doi: 10.1038/nn.4117 pubmed: 26352792
Wolff M, Zhang-Haagen B, Decker C, Barz B, Schneider M, Biehl R, Radulescu A, Strodel B, et al (2017) Aβ42 pentamers/hexamers are the smallest detectable oligomers in solution. Sci Rep 7(1):2493. https://doi.org/10.1038/s41598-017-02370-3
doi: 10.1038/s41598-017-02370-3 pubmed: 28559586 pmcid: 5449387
Ferrone F (1999) Analysis of protein aggregation kinetics. Methods Enzymol 309:256–274. https://doi.org/10.1016/s0076-6879(99)09019-9
doi: 10.1016/s0076-6879(99)09019-9 pubmed: 10507029
Serpell LC (2000) Alzheimer’s amyloid fibrils: structure and assembly. Biochim Biophys Acta 1502(1):16–30. https://doi.org/10.1016/s0925-4439(00)00029-6
doi: 10.1016/s0925-4439(00)00029-6 pubmed: 10899428
Roychaudhuri R, Yang M, Hoshi MM, Teplow DB (2009) Amyloid beta-protein assembly and Alzheimer disease. J Biol Chem 284(8):4749–4753. https://doi.org/10.1074/jbc.R800036200
doi: 10.1074/jbc.R800036200 pubmed: 18845536
Cernescu M, Stark T, Kalden E, Kurz C, Leuner K, Deller T, Göbel M, Eckert GP, et al (2012) Laser-induced liquid bead ion desorption mass spectrometry: an approach to precisely monitor the oligomerization of the β-amyloid peptide. Anal Chem 84(12):5276–5284. https://doi.org/10.1021/ac300258m
doi: 10.1021/ac300258m pubmed: 22594938
Österlund N, Moons R, Ilag LL, Sobott F, Gräslund A (2019) Native ion mobility-mass spectrometry reveals the formation of β-barrel shaped amyloid-β hexamers in a membrane-mimicking environment. J Am Chem Soc 141(26):10440–10450. https://doi.org/10.1021/jacs.9b04596
doi: 10.1021/jacs.9b04596 pubmed: 31141355
Decock M, Stanga S, Octave JN, Dewachter I, Smith SO, Constantinescu SN, Kienlen-Campard P (2016) Glycines from the APP GXXXG/GXXXA transmembrane motifs promote formation of pathogenic aβ oligomers in cells. Front Aging Neurosci 8:107. https://doi.org/10.3389/fnagi.2016.00107
doi: 10.3389/fnagi.2016.00107 pubmed: 27242518 pmcid: 4861705
Vadukul DM, Vrancx C, Burguet P, Contino S, Suelves N, Serpell LC, Quinton L, Kienlen-Campard P (2021) An evaluation of the self-assembly enhancing properties of cell-derived hexameric amyloid-β. Sci Rep 11(1):11570. https://doi.org/10.1038/s41598-021-90680-y
doi: 10.1038/s41598-021-90680-y pubmed: 34078941 pmcid: 8172837
De Strooper B (2003) Aph-1, Pen-2, and nicastrin with presenilin generate an active gamma-Secretase complex. Neuron 38(1):9–12. https://doi.org/10.1016/s0896-6273(03)00205-8
doi: 10.1016/s0896-6273(03)00205-8 pubmed: 12691659
De Strooper B, Saftig P, Craessaerts K, Vanderstichele H, Guhde G, Annaert W, Von Figura K, Van Leuven F (1998) Deficiency of presenilin-1 inhibits the normal cleavage of amyloid precursor protein. Nature 391(6665):387–390. https://doi.org/10.1038/34910
doi: 10.1038/34910 pubmed: 9450754
Frånberg J, Svensson AI, Winblad B, Karlström H, Frykman S (2011) Minor contribution of presenilin 2 for γ-secretase activity in mouse embryonic fibroblasts and adult mouse brain. Biochem Biophys Res Commun 404(1):564–568. https://doi.org/10.1016/j.bbrc.2010.12.029
doi: 10.1016/j.bbrc.2010.12.029 pubmed: 21146496
Pintchovski SA, Schenk DB, Basi GS (2013) Evidence that enzyme processivity mediates differential Aβ production by PS1 and PS2. Curr Alzheimer Res 10(1):4–10. https://doi.org/10.2174/156720513804871480
doi: 10.2174/156720513804871480 pubmed: 22950863 pmcid: 3617584
Xia D, Watanabe H, Wu B, Lee SH, Li Y, Tsvetkov E, Bolshakov VY, Shen J, et al (2015) Presenilin-1 knockin mice reveal loss-of-function mechanism for familial Alzheimer’s disease. Neuron 85(5):967–981. https://doi.org/10.1016/j.neuron.2015.02.010
doi: 10.1016/j.neuron.2015.02.010 pubmed: 25741723 pmcid: 4358812
Stanga S, Vrancx C, Tasiaux B, Marinangeli C, Karlström H, Kienlen-Campard P (2018) Specificity of presenilin-1- and presenilin-2-dependent γ-secretases towards substrate processing. J Cell Mol Med 22(2):823–833. https://doi.org/10.1111/jcmm.13364
doi: 10.1111/jcmm.13364 pubmed: 28994238
Meckler X, Checler F (2016) Presenilin 1 and Presenilin 2 target γ-secretase complexes to distinct cellular compartments. J Biol Chem 291(24):12821–12837. https://doi.org/10.1074/jbc.M115.708297
doi: 10.1074/jbc.M115.708297 pubmed: 27059953 pmcid: 4933450
Sannerud R, Esselens C, Ejsmont P, Mattera R, Rochin L, Tharkeshwar AK, De Baets G, De Wever V, et al (2016) Restricted location of PSEN2/γ-secretase determines substrate specificity and generates an intracellular Aβ pool. Cell 166(1):193–208. https://doi.org/10.1016/j.cell.2016.05.020
doi: 10.1016/j.cell.2016.05.020 pubmed: 27293189 pmcid: 7439524
Lambert MP, Barlow AK, Chromy BA, Edwards C, Freed R, Liosatos M, Morgan TE, Rozovsky I, et al (1998) Diffusible, nonfibrillar ligands derived from Abeta1-42 are potent central nervous system neurotoxins. Proc Natl Acad Sci USA 95(11):6448–6453. https://doi.org/10.1073/pnas.95.11.6448
doi: 10.1073/pnas.95.11.6448 pubmed: 9600986 pmcid: 27787
Lesné S, Koh MT, Kotilinek L, Kayed R, Glabe CG, Yang A, Gallagher M, Ashe KH (2006) A specific amyloid-beta protein assembly in the brain impairs memory. Nature 440(7082):352–357. https://doi.org/10.1038/nature04533
doi: 10.1038/nature04533 pubmed: 16541076
Müller-Schiffmann A, Herring A, Abdel-Hafiz L, Chepkova AN, Schäble S, Wedel D, Horn AH, Sticht H, et al (2016) Amyloid-β dimers in the absence of plaque pathology impair learning and synaptic plasticity. Brain 139(Pt 2):509–525. https://doi.org/10.1093/brain/awv355
doi: 10.1093/brain/awv355 pubmed: 26657517
Shankar GM, Li S, Mehta TH, Garcia-Munoz A, Shepardson NE, Smith I, Brett FM, Farrell MA, et al (2008) Amyloid-beta protein dimers isolated directly from Alzheimer’s brains impair synaptic plasticity and memory. Nat Med 14(8):837–842. https://doi.org/10.1038/nm1782
doi: 10.1038/nm1782 pubmed: 2772133 pmcid: 2772133
Townsend M, Shankar GM, Mehta T, Walsh DM, Selkoe DJ (2006) Effects of secreted oligomers of amyloid beta-protein on hippocampal synaptic plasticity: a potent role for trimers. J Physiol 572(Pt 2):477–492. https://doi.org/10.1113/jphysiol.2005.103754
doi: 10.1113/jphysiol.2005.103754 pubmed: 16469784 pmcid: 1779683
Oakley H, Cole SL, Logan S, Maus E, Shao P, Craft J, Guillozet-Bongaarts A, Ohno M, et al (2006) Intraneuronal beta-amyloid aggregates, neurodegeneration, and neuron loss in transgenic mice with five familial Alzheimer’s disease mutations: potential factors in amyloid plaque formation. J Neurosci 26(40):10129–10140. https://doi.org/10.1523/jneurosci.1202-06.2006
doi: 10.1523/jneurosci.1202-06.2006 pubmed: 17021169 pmcid: 6674618
Kienlen-Campard P, Tasiaux B, Van Hees J, Li M, Huysseune S, Sato T, Fei JZ, Aimoto S, et al (2008) Amyloidogenic processing but not amyloid precursor protein (APP) intracellular C-terminal domain production requires a precisely oriented APP dimer assembled by transmembrane GXXXG motifs. J Biol Chem 283(12):7733–7744. https://doi.org/10.1074/jbc.M707142200
doi: 10.1074/jbc.M707142200 pubmed: 18201969
Huysseune S, Kienlen-Campard P, Hébert S, Tasiaux B, Leroy K, Devuyst O, Brion JP, De Strooper B, et al (2009) Epigenetic control of aquaporin 1 expression by the amyloid precursor protein. FASEB J 23(12):4158–4167. https://doi.org/10.1096/fj.09-140012
doi: 10.1096/fj.09-140012 pubmed: 19687153
Karlström H, Bergman A, Lendahl U, Näslund J, Lundkvist J (2002) A sensitive and quantitative assay for measuring cleavage of presenilin substrates. J Biol Chem 277(9):6763–6766. https://doi.org/10.1074/jbc.C100649200
doi: 10.1074/jbc.C100649200 pubmed: 11744687
Marshall KE, Vadukul DM, Dahal L, Theisen A, Fowler MW, Al-Hilaly Y, Ford L, Kemenes G, et al (2016) A critical role for the self-assembly of Amyloid-β1-42 in neurodegeneration. Sci Rep 6:30182. https://doi.org/10.1038/srep30182
doi: 10.1038/srep30182 pubmed: 27443509 pmcid: 4957119
Hsu PD, Lander ES, Zhang F (2014) Development and applications of CRISPR-Cas9 for genome engineering. Cell 157(6):1262–1278. https://doi.org/10.1016/j.cell.2014.05.010
doi: 10.1016/j.cell.2014.05.010 pubmed: 24906146 pmcid: 24906146
Wiedenheft B, Sternberg SH, Doudna JA (2012) RNA-guided genetic silencing systems in bacteria and archaea. Nature 482(7385):331–338. https://doi.org/10.1038/nature10886
doi: 10.1038/nature10886 pubmed: 22337052
Hage S, Stanga S, Marinangeli C, Octave JN, Dewachter I, Quetin-Leclercq J, Kienlen-Campard P (2015) Characterization of Pterocarpus erinaceus kino extract and its gamma-secretase inhibitory properties. J Ethnopharmacol 163:192–202. https://doi.org/10.1016/j.jep.2015.01.028
doi: 10.1016/j.jep.2015.01.028 pubmed: 25639816
Marinangeli C, Tasiaux B, Opsomer R, Hage S, Sodero AO, Dewachter I, Octave JN, Smith SO, et al (2015) Presenilin transmembrane domain 8 conserved AXXXAXXXG motifs are required for the activity of the γ-secretase complex. J Biol Chem 290(11):7169–7184. https://doi.org/10.1074/jbc.M114.601286
doi: 10.1074/jbc.M114.601286 pubmed: 25614624 pmcid: 4358137
Teunissen CE, Petzold A, Bennett JL, Berven FS, Brundin L, Comabella M, Franciotta D, Frederiksen JL, et al (2009) A consensus protocol for the standardization of cerebrospinal fluid collection and biobanking. Neurology 73(22):1914–1922. https://doi.org/10.1212/WNL.0b013e3181c47cc2
doi: 10.1212/WNL.0b013e3181c47cc2 pubmed: 19949037 pmcid: 2839806
Opsomer R, Contino S, Perrin F, Gualdani R, Tasiaux B, Doyen P, Vergouts M, Vrancx C, et al (2020) Amyloid precursor protein (APP) controls the expression of the transcriptional activator neuronal PAS domain protein 4 (NPAS4) and synaptic GABA release. eNeuro. https://doi.org/10.1523/eneuro.0322-19.2020
doi: 10.1523/eneuro.0322-19.2020 pubmed: 32327470 pmcid: 7262005
Munter LM, Voigt P, Harmeier A, Kaden D, Gottschalk KE, Weise C, Pipkorn R, Schaefer M, et al (2007) GxxxG motifs within the amyloid precursor protein transmembrane sequence are critical for the etiology of Abeta42. EMBO J 26(6):1702–1712. https://doi.org/10.1038/sj.emboj.7601616
doi: 10.1038/sj.emboj.7601616 pubmed: 17332749 pmcid: 1829382
Dehury B, Tang N, Blundell TL, Kepp KP (2019) Structure and dynamics of γ-secretase with presenilin 2 compared to presenilin 1. RSC Adv 9(36):20901–20916. https://doi.org/10.1039/C9RA02623A
doi: 10.1039/C9RA02623A
Lauritzen I, Pardossi-Piquard R, Bourgeois A, Pagnotta S, Biferi MG, Barkats M, Lacor P, Klein W, et al (2016) Intraneuronal aggregation of the β-CTF fragment of APP (C99) induces Aβ-independent lysosomal-autophagic pathology. Acta Neuropathol 132(2):257–276. https://doi.org/10.1007/s00401-016-1577-6
doi: 10.1007/s00401-016-1577-6 pubmed: 27138984 pmcid: 4947121
Evrard C, Kienlen-Campard P, Coevoet M, Opsomer R, Tasiaux B, Melnyk P, Octave JN, Buée L, et al (2018) Contribution of the endosomal-lysosomal and proteasomal systems in amyloid-β precursor protein derived fragments processing. Front Cell Neurosci 12:435. https://doi.org/10.3389/fncel.2018.00435
doi: 10.3389/fncel.2018.00435 pubmed: 30524243 pmcid: 6263093
Perrin F, Papadopoulos N, Suelves N, Opsomer R, Vadukul DM, Vrancx C, Smith SO, Vertommen D, et al (2020) Dimeric transmembrane orientations of APP/C99 regulate γ-secretase processing line impacting signaling and oligomerization. ISCIENCE. https://doi.org/10.1016/j.isci.2020.101887
doi: 10.1016/j.isci.2020.101887 pubmed: 33367225 pmcid: 7749410
Rajendran L, Honsho M, Zahn TR, Keller P, Geiger KD, Verkade P, Simons K (2006) Alzheimer’s disease beta-amyloid peptides are released in association with exosomes. Proc Natl Acad Sci USA 103(30):11172–11177. https://doi.org/10.1073/pnas.0603838103
doi: 10.1073/pnas.0603838103 pubmed: 16837572 pmcid: 1544060
Eimer WA, Vassar R (2013) Neuron loss in the 5XFAD mouse model of Alzheimer’s disease correlates with intraneuronal Aβ42 accumulation and Caspase-3 activation. Mol Neurodegener 8:2. https://doi.org/10.1186/1750-1326-8-2
doi: 10.1186/1750-1326-8-2 pubmed: 23316765 pmcid: 3552866
Doecke JD, Pérez-Grijalba V, Fandos N, Fowler C, Villemagne VL, Masters CL, Pesini P, Sarasa M (2020) Total Aβ(42)/Aβ(40) ratio in plasma predicts amyloid-PET status, independent of clinical AD diagnosis. Neurology 94(15):e1580–e1591. https://doi.org/10.1212/wnl.0000000000009240
doi: 10.1212/wnl.0000000000009240 pubmed: 32179698 pmcid: 7251518
Gravina SA, Ho L, Eckman CB, Long KE, Otvos L, Younkin LH, Suzuki N, Younkin SG (1995) Amyloid beta protein (A beta) in Alzheimer’s disease brain. Biochemical and immunocytochemical analysis with antibodies specific for forms ending at A beta 40 or A beta 42(43). J Biol Chem 270(13):7013–7016. https://doi.org/10.1074/jbc.270.13.7013
doi: 10.1074/jbc.270.13.7013 pubmed: 7706234
Jarrett JT, Berger EP, Lansbury PT Jr (1993) The carboxy terminus of the beta amyloid protein is critical for the seeding of amyloid formation: implications for the pathogenesis of Alzheimer’s disease. Biochemistry 32(18):4693–4697. https://doi.org/10.1021/bi00069a001
doi: 10.1021/bi00069a001 pubmed: 8490014 pmcid: 8490014
Li X, Buxbaum JN (2011) Transthyretin and the brain re-visited: is neuronal synthesis of transthyretin protective in Alzheimer’s disease? Mol Neurodegener 6:79. https://doi.org/10.1186/1750-1326-6-79
doi: 10.1186/1750-1326-6-79 pubmed: 22112803 pmcid: 3267701
Kim H, Kim B, Kim HS, Cho JY (2020) Nicotinamide attenuates the decrease in dendritic spine density in hippocampal primary neurons from 5xFAD mice, an Alzheimer’s disease animal model. Mol Brain 13(1):17. https://doi.org/10.1186/s13041-020-0565-x
doi: 10.1186/s13041-020-0565-x pubmed: 32033569 pmcid: 7006216
Mariani MM, Malm T, Lamb R, Jay TR, Neilson L, Casali B, Medarametla L, Landreth GE (2017) Neuronally-directed effects of RXR activation in a mouse model of Alzheimer’s disease. Sci Rep 7:42270. https://doi.org/10.1038/srep42270
doi: 10.1038/srep42270 pubmed: 28205585 pmcid: 5311933
Noh H, Park C, Park S, Lee YS, Cho SY, Seo H (2014) Prediction of miRNA-mRNA associations in Alzheimer’s disease mice using network topology. BMC Genomics 15(1):644. https://doi.org/10.1186/1471-2164-15-644
doi: 10.1186/1471-2164-15-644 pubmed: 25086961 pmcid: 4132902
Roychaudhuri R, Yang M, Deshpande A, Cole GM, Frautschy S, Lomakin A, Benedek GB, Teplow DB (2013) C-terminal turn stability determines assembly differences between Aβ40 and Aβ42. J Mol Biol 425(2):292–308. https://doi.org/10.1016/j.jmb.2012.11.006
doi: 10.1016/j.jmb.2012.11.006 pubmed: 23154165
Lendel C, Bjerring M, Dubnovitsky A, Kelly RT, Filippov A, Antzutkin ON, Nielsen NC, Härd T (2014) A hexameric peptide barrel as building block of amyloid-β protofibrils. Angew Chem Int Ed Engl 53(47):12756–12760. https://doi.org/10.1002/anie.201406357
doi: 10.1002/anie.201406357 pubmed: 25256598
Bayer TA, Wirths O (2011) Intraneuronal Aβ as a trigger for neuron loss: can this be translated into human pathology? Biochem Soc Trans 39(4):857–861. https://doi.org/10.1042/bst0390857
doi: 10.1042/bst0390857 pubmed: 21787313
Friedrich RP, Tepper K, Rönicke R, Soom M, Westermann M, Reymann K, Kaether C, Fändrich M (2010) Mechanism of amyloid plaque formation suggests an intracellular basis of Abeta pathogenicity. Proc Natl Acad Sci USA 107(5):1942–1947. https://doi.org/10.1073/pnas.0904532106
doi: 10.1073/pnas.0904532106 pubmed: 20133839 pmcid: 2836607
Gouras GK, Tampellini D, Takahashi RH, Capetillo-Zarate E (2010) Intraneuronal beta-amyloid accumulation and synapse pathology in Alzheimer’s disease. Acta Neuropathol 119(5):523–541. https://doi.org/10.1007/s00401-010-0679-9
doi: 10.1007/s00401-010-0679-9 pubmed: 20354705 pmcid: 3183823
Pensalfini A, Albay R 3rd, Rasool S, Wu JW, Hatami A, Arai H, Margol L, Milton S, et al (2014) Intracellular amyloid and the neuronal origin of Alzheimer neuritic plaques. Neurobiol Dis 71:53–61. https://doi.org/10.1016/j.nbd.2014.07.011
doi: 10.1016/j.nbd.2014.07.011 pubmed: 25092575
Jack CR Jr, Knopman DS, Jagust WJ, Shaw LM, Aisen PS, Weiner MW, Petersen RC, Trojanowski JQ (2010) Hypothetical model of dynamic biomarkers of the Alzheimer’s pathological cascade. Lancet Neurol 9(1):119–128. https://doi.org/10.1016/s1474-4422(09)70299-6
doi: 10.1016/s1474-4422(09)70299-6 pubmed: 20083042 pmcid: 2819840
Castelletto V, Ryumin P, Cramer R, Hamley IW, Taylor M, Allsop D, Reza M, Ruokolainen J, et al (2017) Self-assembly and Anti-amyloid cytotoxicity activity of amyloid beta peptide derivatives. Sci Rep 7:43637. https://doi.org/10.1038/srep43637
doi: 10.1038/srep43637 pubmed: 28272542 pmcid: 5341572
Morales R, Callegari K, Soto C (2015) Prion-like features of misfolded Aβ and tau aggregates. Virus Res 207:106–112. https://doi.org/10.1016/j.virusres.2014.12.031
doi: 10.1016/j.virusres.2014.12.031 pubmed: 25575736
Katzmarski N, Ziegler-Waldkirch S, Scheffler N, Witt C, Abou-Ajram C, Nuscher B, Prinz M, Haass C, et al (2020) Aβ oligomers trigger and accelerate Aβ seeding. Brain Pathol 30(1):36–45. https://doi.org/10.1111/bpa.12734
doi: 10.1111/bpa.12734 pubmed: 31099449

Auteurs

Céline Vrancx (C)

Alzheimer Research Group, Cellular and Molecular Division (CEMO), Institute of Neuroscience, Université Catholique de Louvain, 1200, Brussels, Belgium.

Devkee M Vadukul (DM)

Alzheimer Research Group, Cellular and Molecular Division (CEMO), Institute of Neuroscience, Université Catholique de Louvain, 1200, Brussels, Belgium.

Nuria Suelves (N)

Alzheimer Research Group, Cellular and Molecular Division (CEMO), Institute of Neuroscience, Université Catholique de Louvain, 1200, Brussels, Belgium.

Sabrina Contino (S)

Alzheimer Research Group, Cellular and Molecular Division (CEMO), Institute of Neuroscience, Université Catholique de Louvain, 1200, Brussels, Belgium.

Ludovic D'Auria (L)

Neurochemistry Unit, Cellular and Molecular Division (CEMO), Institute of Neuroscience, Université Catholique de Louvain, 1200, Brussels, Belgium.

Florian Perrin (F)

Alzheimer Research Group, Cellular and Molecular Division (CEMO), Institute of Neuroscience, Université Catholique de Louvain, 1200, Brussels, Belgium.

Vincent van Pesch (V)

Neurochemistry Unit, Cellular and Molecular Division (CEMO), Institute of Neuroscience, Université Catholique de Louvain, 1200, Brussels, Belgium.

Bernard Hanseeuw (B)

Department of Neurology, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, 1200, Brussels, Belgium.

Loïc Quinton (L)

Laboratory of Mass Spectrometry, Department of Chemistry, Université de Liège, 4000, Liège, Belgium.

Pascal Kienlen-Campard (P)

Alzheimer Research Group, Cellular and Molecular Division (CEMO), Institute of Neuroscience, Université Catholique de Louvain, 1200, Brussels, Belgium. pascal.kienlen-campard@uclouvain.be.

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Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH