The DOI matches its Crossref record; 38 of the 38 references it cites were found in a registry or an index.
Intracellular Aβ and cognitive deficits precede β-amyloid deposition in transgenic arcAβ mice
Abstract
The brain pathology of Alzheimer's disease is characterized by abnormally aggregated Abeta in extracellular beta-amyloid plaques and along blood vessel walls, but the relation to intracellular Abeta remains unclear. To address the role of intracellular Abeta deposition in vivo, we expressed human APP with the combined Swedish and Arctic mutations in mice (arcAbeta mice). Intracellular punctate deposits of Abeta occurred concomitantly with robust cognitive impairments at the age of 6 months before the onset of beta-amyloid plaque formation and cerebral beta-amyloid angiopathy. beta-Amyloid plaques from arcAbeta mice had distinct dense-core morphologies with blood vessels appearing as seeding origins, suggesting reduced clearance of Abeta across blood vessels in arcAbeta mice. The co-incidence of intracellular Abeta deposits with behavioral deficits support an early role of intracellular Abeta in the pathophysiological cascade leading to beta-amyloid formation and functional impairment.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Furthermore, several AD Tg animal models are characterized by early and massive intraneuronal accumulation of Ab oligomers, loss of synaptic proteins, and behavioral impairment which occur in the absence of extracellular Ab plaques.7,51”
From Blocking the Interaction between Apolipoprotein E and Aβ Reduces Intraneuronal Accumulation of Aβ and Inhibits Synaptic Degeneration (2013) · cites this paper as [51]
In the citing paper
“FAD transgenic mouse models with the highest level of amyloidogenic Aβ display particularly prominent early intraneuronal Aβ accumulation [89, 106, 196].”
From Intraneuronal β-amyloid accumulation and synapse pathology in Alzheimer’s disease (2010) · cites this paper as [89]
Citations
Cites
1 retracted
RETRACTED ARTICLE: A specific amyloid-β protein assembly in the brain impairs memory
Lesné, S., Koh, M. T., Kotilinek, L., Kayed, R., Glabe, C. G., Yang, A., Gallagher, M., & Ashe, K. H. (2006) · Nature · doi:10.1038/nature04533 · Cited by 2,769
RetractedAlzheimer's disease: the amyloid cascade hypothesis
Hardy, J. A., & Higgins, G. A. (1992) · Science · doi:10.1126/science.1566067 · Cited by 7,484
Walsh, D. M., Klyubin, I., Fadeeva, J. V., Cullen, W. K., Anwyl, R., Wolfe, M. S., Rowan, M. J., & Selkoe, D. J. (2002) · Nature · doi:10.1038/416535a · Cited by 4,291
Correlative Memory Deficits, Aβ Elevation, and Amyloid Plaques in Transgenic Mice
Hsiao, K., Chapman, P., Nilsen, S., Eckman, C., Harigaya, Y., Younkin, S., Yang, F., & Cole, G. (1996) · Science · doi:10.1126/science.274.5284.99 · Cited by 4,210
Diffusible, nonfibrillar ligands derived from Aβ 1–42 are potent central nervous system neurotoxins
Lambert, M. P., Barlow, A. K., Chromy, B. A., Edwards, C., Freed, R., Liosatos, M., Morgan, T. E., Rozovsky, I., Trommer, B., Viola, K. L., et al. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.11.6448 · Cited by 3,506
Neurofibrillary tangles but not senile plaques parallel duration and severity of Alzheimer's disease
Arriagada, P. V., Growdon, J. H., Hedley-Whyte, E. T., & Hyman, B. T. (1992) · Neurology · doi:10.1212/wnl.42.3.631 · Cited by 2,668
Natural oligomers of the amyloid-β protein specifically disrupt cognitive function
Cleary, J. P., Walsh, D. M., Hofmeister, J. J., Shankar, G. M., Kuskowski, M. A., Selkoe, D. J., & Ashe, K. H. (2004) · Nature Neuroscience · doi:10.1038/nn1372 · Cited by 1,722
Formation of Neurofibrillary Tangles in P301L Tau Transgenic Mice Induced by Aβ42 Fibrils
Götz, J., Chen, F., van Dorpe, J., & Nitsch, R. M. (2001) · Science · doi:10.1126/science.1062097 · Cited by 1,526
Self-citationMullan, M., Crawford, F., Axelman, K., Houlden, H., Lilius, L., Winblad, B., & Lannfelt, L. (1992) · Nature Genetics · doi:10.1038/ng0892-345 · Cited by 1,513
Oligomeric and fibrillar species of amyloid-β peptides differentially affect neuronal viability
Dahlgren, K. N., Manelli, A. M., Stine, W. B., Baker, L. K., Krafft, G. A., & LaDu, M. J. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m201750200 · Cited by 1,452
Cited by
Sorted by citations
Items 201–257 of 257
Heat Shock Proteins and Protein Quality Control in Alzheimer’s Disease
van Leeuwen, F. W., & Kampinga, H. H. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-811304-2.00010-9 · Cited by 9
Бунеева, О. А., Gnedenko, O. V., Medvedeva, M. V., Ivanov, A. S., & Medvedev, A. E. (2016) · Biomeditsinskaya Khimiya · doi:10.18097/pbmc20166206720 · Cited by 8
Light on Alzheimer’s disease: from basic insights to preclinical studies
Mi, J., Liu, C., Chen, H., Qian, Y., Zhu, J., Zhang, Y., Liang, Y., Wang, L., & Ta, D. (2024) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2024.1363458 · Cited by 8
Hofmann, C., Sander, A., Wang, X. X., Buerge, M., Jungwirth, B., Borgstedt, L., Kreuzer, M., Kopp, C., Schorpp, K., Hadian, K., et al. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-201185 · Cited by 7
BIN1 in the Pursuit of Ousting the Alzheimer’s Reign: Impact on Amyloid and Tau Neuropathology
Kaur, I., Behl, T., Sundararajan, G., Panneerselvam, P., Vijayakumar, A. R., Senthilkumar, G. P., Venkatachalam, T., Jaglan, D., Yadav, S., Anwer, K., et al. (2023) · Neurotoxicity Research · doi:10.1007/s12640-023-00670-3 · Cited by 6
Hilt, S., Liu, R., Maezawa, I., Rojalin, T., Aung, H. H., Budamagunta, M. S., Slez, R. R., Gong, Q., Carney, R. P., & Voss, J. C. (2022) · Frontiers in Chemistry · doi:10.3389/fchem.2022.896386 · Cited by 7
The Arctic/Swedish APP mutation alters the impact of chronic stress on cognition in mice
Cortese, A., Delgado‐Morales, R., Almeida, O. F. X., & Romberg, C. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14500 · Cited by 7
El populismo: de intruso a problema relevante para la ciencia social
Sáez, A. R. (2018) · Revista Internacional de Sociología · doi:10.3989/ris.2018.76.4.18.076 · Cited by 6
Gu, S., & Ran, C. (2025) · iRadiology · doi:10.1002/ird3.70002 · Cited by 5
Eyvani, K., Letafatkar, N., & Babaei, P. (2024) · Experimental Aging Research · doi:10.1080/0361073x.2024.2377440 · Cited by 5
Emerging Roles of Mitochondrial Serine Protease HtrA2 in Neurodegeneration
Wagh, A. R., & Bose, K. (2017) · Springer eBooks · doi:10.1007/978-981-10-2513-6_15 · Cited by 5
Koch‐Paszkowski, J., Sennett, C., & Pula, G. (2025) · Cells · doi:10.3390/cells14141069 · Cited by 5
Bulgart, H. R., Perez, M. A. L., Tucker, A., Giarrano, G. N., Banford, K. K., Miller, O., Bonser, S. W. G., Wold, L. E., Scharre, D. W., & Weisleder, N. L. (2024) · The FASEB Journal · doi:10.1096/fj.202401731rr · Cited by 4
Brosens, N., Samouil, D., Stolker, S., Katsika, E. V., Weggen, S., Lucassen, P. J., & Krugers, H. J. (2023) · Journal of Alzheimer s Disease · doi:10.3233/jad-230727 · Cited by 4
Salazar, J., Samhan-Arias, A. K., & Gutiérrez‐Merino, C. (2023) · Molecules · doi:10.3390/molecules28207138 · Cited by 4
Bansal, V. A., Tan, J. M., Soon, H. R., Zainolabidin, N., Saido, T. C., & Ch’ng, T. H. (2024) · eLife · doi:10.7554/elife.92069.3 · Cited by 4
I J, O., S A, N., E E, E., F S, B., & E M, O. (2018) · International Journal of Pharmacology and Toxicology · doi:10.14419/ijpt.v6i2.13578 · Cited by 2
Disrupted structural connectivity in ArcAβ mouse model of Aβ amyloidosis
Al-Amin, M. M., Grandjean, J., Klohs, J., & Kim, J. (2020) · doi:10.1101/2020.04.27.064634 · Cited by 2
“Aβ plaque deposition and impaired cognitive function begins at 6 months (Knobloch et al., 2007b), with vascular Aβ appearing between 9 and 15 months (Merlini et al., 2011).”
BackgroundInfluentialRiffo-Lepe, N., González-Sanmiguel, J., Armijo‐Weingart, L., Saavedra, P., Hernandez, D., Ramos, G., Martín, L. S., & Aguayo, L. G. (2025) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-24-01052 · Cited by 2
Heat Shock Proteins, Unfolded Protein Response Chaperones and Alzheimer’s Disease
Magrané, J., & Querfurth, H. W. (2008) · Springer eBooks · doi:10.1007/978-1-4020-8231-3_2 · Cited by 2
Anti-amyloid β hydrophobic peptides in Alzheimer’s disease: biomarkers and therapeutic potential
Gutiérrez‐Merino, C. (2025) · Exploration of neuroscience · doi:10.37349/en.2025.100672 · Cited by 2
Gutiérrez‐Merino, C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241813846 · Cited by 4
Membrane Trafficking and Targeting in Alzheimer's Disease
Rajendran, L., & Simons, K. (2009) · Research and perspectives in Alzheimer's disease · doi:10.1007/978-3-540-87941-1_8 · Cited by 2
Early Intraneuronal β-Amyloid Pathology: Do Transgenic Mice Represent Valid Model Systems?
Wirths, O., & Bayer, T. A. (2008) · Open Longevity Science · doi:10.2174/1874369200802010007 · Cited by 2
Riemann, K., von Ahsen, J., Böhm, T., Schlegel, M., Kreuzer, M., Fenzl, T., Russ, H., Parsons, C. G., & Rammes, G. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26094167 · Cited by 1
Transcriptional and post-transcriptional responses to amyloid- β in cerebral amyloid angiopathy
Florijn, B. W., Verwey, N. A., van Etten, E. S., de Vries, H. E., & Wermer, M. J. H. (2025) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x251366082 · Cited by 1
Protein seeding in Alzheimer’s disease and Parkinson’s disease: Similarities and differences
Ibrahim, T. (2014) · World Journal of Neurology · doi:10.5316/wjn.v4.i4.23 · Cited by 1
Role of Reactive Astrocytes in Alzheimer’s Disease
Sarkar, S., Guha, S., & Biswas, S. C. (2022) · Springer eBooks · doi:10.1007/978-981-16-8313-8_9 · Cited by 1
Animal Models of Menopausal Metabolism
Banu, J., & Fernandes, G. (2013) · Humana Press eBooks · doi:10.1007/978-1-62703-373-2_29 · Cited by 1
Tackenberg, C. (2016) · Matters · doi:10.19185/matters.201602000028 · Cited by 1
FMRI in Mice: Functional Phenotyping of Transgenic Mouse Lines Based on Hemodynamic Readouts
Mueggler, T., Baltes, C., Bosshard, S. C., Princz-Kranz, F. L., Ratering, D., Razoux, F., Sydekum, E., & Rudin, M. (2011) · Advances in neurobiology · doi:10.1007/978-1-4614-1788-0_18 · Cited by 1
Modeling Amyloid Disease in Drosophila melanogaster
Berg, I. (2010) · KTH Publication Database DiVA (KTH Royal Institute of Technology) · Cited by 1
Intracellular Amyloid β: A Modification to the Amyloid Hypothesis in Alzheimer's Disease
Zhang, Y. (2011) · Wiley eBooks · doi:10.1002/9783527634323.ch6 · Cited by 1
Automated behavioral phenotyping of inbred mouse strains and mouse models of Alzheimer disease
Codita, A. (2011) · Figshare · Cited by 1
IMPAIRED BRIDGING OF TEMPORAL DISCONTINUITIES IN OLDER ADULT HIV-1 TG RATSPreprint
McLaurin, K. A., Li, H., Ritchie, A., Booze, R. M., & Mactutus, C. F. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.04.06.716768 · Cited by 1
Targeting Early Stages of Alzheimer’s Disease in a Transgenic Model
Lord, A. (2009) · KTH Publication Database DiVA (KTH Royal Institute of Technology)
Deregulation of oxidative phosphorylation system and energy homeostasis in Alzheimer's disease
Rhein, V. F. (2009) · edoc (University of Basel) · doi:10.5451/unibas-005042311
Koo, J., Eum, H.-S., Kang, E., Kwon, I., Yeom, D.-C., An, G.-Y., Oh, Y.-S., Baik, Y.-S., Cho, I.-H., & Cho, J. (2010) · Journal of Life Science · doi:10.5352/jls.2010.20.3.444
Pathogenic mechanisms of the Arctic Alzheimer mutation.
Sahlin, C. (2007) · Uppsala University Publications (Uppsala University)
Murtishaw, A. S. (2020) · Digital Scholarship - UNLV (University of Nevada Reno) · doi:10.34917/6456429
Liu, J., Miki, T., Matsumoto, Y., Ohta, K., Suzuki, S., Warita, K., Yakura, T., Tamai, M., & Takeuchi, Y. (2013) · Institutional Repositories DataBase (IRDB)
Pathological Consequences of Aβ From Extracellular to Intraneuronal
D’Andrea, M. R. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-804256-4.00004-8
Intraneuronal Amyloid and Plaque Formation
D’Andrea, M. R. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-804256-4.00005-x
Intraneuronal Amyloid and Cognitive Impairment
D’Andrea, M. R. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-804256-4.00006-1
Dupont, G. (2013) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.717982127.793481028
IMPACTS OF HYPERTENSION AND THROMBOSIS IN A RAT MODEL OF CEREBRAL AMYLOID ANGIOPATHY (rTg-DI)
Stanisavljevic, A. (2022) · Digital Commons - URI (University of Rhode Island) · doi:10.23860/diss-stanisavljevic-aleksandra-2022
Bansal, V. A., Tan, J. M., Soon, H. R., Zainolabidin, N., Saito, T., & Ch’ng, T. H. (2024) · eLife · doi:10.7554/elife.92069.1
Ito, S., Yamauchi, K., Hama, H., Koike, M., Miyawaki, A., & Hioki, H. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.04.25.591057
Bansal, V. A., Tan, J. M., Soon, H. R., Zainolabidin, N., Saito, T., & Ch’ng, T. H. (2024) · eLife · doi:10.7554/elife.92069.2
Budamagunta, M. S., Mori, H., Silk, J., Slez, R. R., Bognár, B., Mendiola, U. R., Kálai, T., Maezawa, I., & Voss, J. C. (2024) · Antioxidants · doi:10.3390/antiox13111411
Bansal, V. A., Tan, J. M., Soon, H. R., Zainolabidin, N., Saido, T. C., & Ch’ng, T. H. (2025) · eLife · doi:10.7554/elife.92069.3.sa3
Rouault, M., Kindler, D., Ni, R., Liberale, L., Seiler, R., Ielacqua, G. D., Nitsch, R. M., Pryce, C. R., Camici, G. G., Kulic, L., et al. (2026) · Aging Brain · doi:10.1016/j.nbas.2026.100167
Self-citationA silent RAGE: The inflammatory pathway to dementia in Parkinson’s disease
Peixoto, D. O., Gasparotto, J., Ojo, O. R., Aro, O. P., Godswill, U.-A. S., de Abreu, L. F., Lopes, L. C., Moreira, J. C. F., & Gelain, D. P. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103392
The molecular basis of the interactions of copper metallochaperones
Aggarwal, S. (2011)
Metadata
- Authors
- Knobloch, M., Konietzko, U., Krebs, D. C., & Nitsch, R. M.
- Affiliations
- University of Zurich (CH)
- Corresponding author
- Nitsch, Roger M.
- Venue
- Neurobiology of Aging
- Publisher
- Elsevier BV
- Published
- 2007-09
- Volume
- 28
- Issue
- 9
- Pages
- 1297-1306
- ISSN
- 0197-4580 (ISSN-L)
- OpenAlex
- W2006696380
- Cited by
- 259
- References
- 38
- Citations by year
- 2026: 4 · 2025: 8 · 2024: 15 · 2023: 15 · 2022: 17 · 2021: 10 · 2020: 11 · 2019: 7 · 2018: 11 · 2017: 10 · 2016: 20 · 2015: 15 · 2014: 12 · 2013: 11 · 2012: 17
- FWCI
- 7.75
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neurobiology of Aging (publishedVersion)
- PubMed (publishedVersion)
- Zurich Open Repository and Archive (University of Zurich) (submittedVersion)
- Funders
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (3200B0-112616)
- European Commission (6027, LSHM-CT-2003-503330)
- nccr – on the move
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- Alzheimer's disease, APP transgenic mice, cognitive impairment, amyloid plaques, cerebral amyloid angiopathy, amyloid clearance, amyloid seeding, APP mutations
- MeSH terms
- Age Factors, Analysis of Variance, Animals, Avoidance Learning, Behavior, Animal, Cognition Disorders, Exploratory Behavior, Humans, Mice, Inbred C57BL, Mice, Transgenic, Motor Activity, Mutation, Neurologic Examination, Amyloid beta-Peptides, Amyloid beta-Protein Precursor, Maze Learning, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization, Rotarod Performance Test, Mice, Plaque, Amyloid
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review