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Autophagy in Alzheimer’s disease
Open accessAbstract
Autophagy is a vesicle and lysosome-mediated degradative pathway that is essential for protein homeostasis and cell health. In particular, compared to nonneuronal cells, neurons are dependent on high basal autophagy for survival. There is emerging agreement that defects in autophagy are likely to contribute to the neurodegenerative processes in numerous diseases, including Alzheimer’s disease (AD). Autophagy-lysosome defects occur early in the pathogenesis of AD and have been proposed to be a significant contributor to the disease process. Given the fact that autophagy deficits are likely major contributors to the etiology of AD, the focus of this review will be on recent studies that support a role for autophagy deficits in AD.
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“Impairment of protein degradation pathways, including autophagy (reviewed previously66–68), is found in a host of neurodegenerative diseases.”
From Tau-targeting therapies for Alzheimer disease (2018) · cites this paper as [67]
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Cites
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
Li, Y., Jiang, Q. L., Cao, G.-F., Yao, J., & Yan, B. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000373980 · Cited by 16,351
LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing.
Kabeya, Y., Mizushima, N., Ueno, T., Yamamoto, A., Kirisako, T., Noda, T., Kominami, E., Ohsumi, Y., & Yoshimori, T. (2000) · The EMBO Journal · doi:10.1093/emboj/19.21.5720 · Cited by 6,605
Cui, C., Cui, J., Jin, F., Cui, Y., Li, R., Jiang, X., Tian, Y., Wang, R. C., Jiang, P., & Gao, J. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000479571 · Cited by 5,214
Cillà, S. D., Farruggio, S., Vujosevic, S., Raina, G., Filippini, D. A., Gatti, V., Clemente, N., Mary, D., Vezzola, D., Casini, G., et al. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000479441 · Cited by 5,154
Pankiv, S., Clausen, T. H., Lamark, T., Brech, A., Bruun, J.-A., Outzen, H., Øvervatn, A., Bjørkøy, G., & Johansen, T. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m702824200 · Cited by 4,578
Querfurth, H. W., & LaFerla, F. M. (2010) · New England Journal of Medicine · doi:10.1056/nejmra0909142 · Cited by 4,569
Upstream and downstream of mTOR
Hay, N., & Sonenberg, N. (2004) · Genes & Development · doi:10.1101/gad.1212704 · Cited by 4,181
TFEB Links Autophagy to Lysosomal Biogenesis
Settembre, C., Di Malta, C., Polito, V. A., Arencibia, M. G., Vetrini, F., Erdin, S., Erdin, S. U., Huynh, T., Medina, D., Colella, P., et al. (2011) · Science · doi:10.1126/science.1204592 · Cited by 3,365
Bjørkøy, G., Lamark, T., Brech, A., Outzen, H., Perander, M., Øvervatn, A., Stenmark, H., & Johansen, T. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200507002 · Cited by 3,276
Kim, D., Sarbassov, D. D., Ali, S. M., King, J. E., Latek, R. R., Erdjument‐Bromage, H., Tempst, P., & Sabatini, D. M. (2002) · Cell · doi:10.1016/s0092-8674(02)00808-5 · Cited by 3,051
Sancak, Y., Bar-Peled, L., Zoncu, R., Markhard, A. L., Nada, S., & Sabatini, D. M. (2010) · Cell · doi:10.1016/j.cell.2010.02.024 · Cited by 2,464 · cited 2×
“dependent fashion—to the lysosomal surface [16, 28].”
Synapse loss in frontal cortex biopsies in Alzheimer's disease: Correlation with cognitive severity
DeKosky, S. T., & Scheff, S. W. (1990) · Annals of Neurology · doi:10.1002/ana.410270502 · Cited by 2,376
Nutrient-dependent mTORC1 Association with the ULK1–Atg13–FIP200 Complex Required for Autophagy
Hosokawa, N., Hara, T., Kaizuka, T., Kishi, C., Takamura, A., Miura, Y., Iemura, S.-I., Natsume, T., Takehana, K., Yamada, N., et al. (2009) · Molecular Biology of the Cell · doi:10.1091/mbc.e08-12-1248 · Cited by 2,076
Selective autophagy mediated by autophagic adapter proteins
Johansen, T., & Lamark, T. (2011) · Autophagy · doi:10.4161/auto.7.3.14487 · Cited by 1,788
The roles of intracellular protein-degradation pathways in neurodegeneration
Rubinsztein, D. C. (2006) · Nature · doi:10.1038/nature05291 · Cited by 1,625
-Synuclein in Parkinson's Disease
Stefanis, L. (2012) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a009399 · Cited by 1,446
Autophagy, mitochondria and oxidative stress: cross-talk and redox signalling.
Lee, J., Giordano, S., & Zhang, J. (2012) · Biochemical Journal · doi:10.1042/bj20111451 · Cited by 1,438
A Role for Ubiquitin in Selective Autophagy
Kirkin, V., McEwan, D. G., Novak, I., & Đikić, I. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.04.026 · Cited by 1,268
Lee, J.-H., Yu, W. H., Kumar, A., Lee, S., Mohan, P. S., Peterhoff, C. M., Wolfe, D. M., Martinez-Vicente, M., Massey, A. C., Sovak, G., et al. (2010) · Cell · doi:10.1016/j.cell.2010.05.008 · Cited by 1,212
Sarkar, S., Davies, J. E., Huang, Z., Tunnacliffe, A., & Rubinsztein, D. C. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m609532200 · Cited by 1,142
Boland, B., Kumar, A., Lee, S., Platt, F. M., Wegiel, J., Yu, W. H., & Nixon, R. A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0800-08.2008 · Cited by 1,119
A Role for NBR1 in Autophagosomal Degradation of Ubiquitinated Substrates
Kirkin, V., Lamark, T., Sou, Y.-S., Bjørkøy, G., Nunn, J. L., Bruun, J.-A., Shvets, E., McEwan, D. G., Clausen, T. H., Wild, P., et al. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.01.020 · Cited by 1,065
Spilman, P., Podlutskaya, N., Hart, M. J., Debnath, J., Gorostiza, O., Bredesen, D., Richardson, A., Strong, R., & Galvan, V. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009979 · Cited by 1,033
Hippocampal synaptic loss in early Alzheimer's disease and mild cognitive impairment
Scheff, S. W., Price, D. A., Schmitt, F. A., & Mufson, E. J. (2006) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2005.09.012 · Cited by 1,017
Discovery of Atg5/Atg7-independent alternative macroautophagy
Nishida, Y., Arakawa, S., Fujitani, K., Yamaguchi, H., Mizuta, T., Kanaseki, T., Komatsu, M., Otsu, K., Tsujimoto, Y., & Shimizu, S. (2009) · Nature · doi:10.1038/nature08455 · Cited by 1,001
Macroautophagy—a novel β-amyloid peptide-generating pathway activated in Alzheimer's disease
Yu, W. H., Cuervo, A. M., Kumar, A., Peterhoff, C. M., Schmidt, S. D., Lee, J.-H., Mohan, P. S., Mercken, M., Farmery, M. R., Tjernberg, L. O., et al. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200505082 · Cited by 967
Impaired synaptic plasticity and learning in aged amyloid precursor protein transgenic mice
Chapman, P. F., White, G. L., Jones, M. W., Cooper-Blacketer, D., Marshall, V. J., Irizarry, M., Younkin, L., Good, M. A., Bliss, T. V. P., Hyman, B. T., et al. (1999) · Nature Neuroscience · doi:10.1038/6374 · Cited by 946
Microautophagy: lesser-known self-eating
Li, W., Li, J., & Bao, J. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0865-5 · Cited by 889
Molecular Interplay between Mammalian Target of Rapamycin (mTOR), Amyloid-β, and Tau
Caccamo, A., Majumder, S., Richardson, A., Strong, R., & Oddo, S. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.100420 · Cited by 881
Peptide sequences that target cytosolic proteins for lysosomal proteolysis
Dice, J. F. (1990) · Trends in Biochemical Sciences · doi:10.1016/0968-0004(90)90019-8 · Cited by 755
CHIP and Hsp70 regulate tau ubiquitination, degradation and aggregation
Petrucelli, L. (2004) · Human Molecular Genetics · doi:10.1093/hmg/ddh083 · Cited by 723 · cited 1×
“There are reports that have demonstrated UPS as a principal τ degradation system (David et al., 2002; Petrucelli et al., 2004; Zhang et al., 2005; Dickey et al., 2007).”
Lipinski, M. M., Zheng, B., Lu, T., Yan, Z., Py, B. F., Ng, A., Xavier, R. J., Li, C., Yankner, B. A., Scherzer, C. R., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1009485107 · Cited by 680
Martina, J. A., Diab, H. I., Lishu, L., Jeong-A, L., Patange, S., Raben, N., & Puertollano, R. (2014) · Science Signaling · doi:10.1126/scisignal.2004754 · Cited by 677
Rapamycin alleviates toxicity of different aggregate-prone proteins
Berger, Z., Ravikumar, B., Menzies, F. M., Oroz, L. G., Underwood, B. R., Pangalos, M. N., Schmitt, I., Wullner, U., Evert, B. O., O'Kane, C. J., et al. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddi458 · Cited by 657
Vingtdeux, V., Giliberto, L., Zhao, H., Chandakkar, P., Wu, Q., Simon, J. E., Janle, E. M., Lobo, J., Ferruzzi, M. G., Davies, P. J., et al. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.060061 · Cited by 654
Dickey, C. A., Kamal, A., Lundgren, K., Klosak, N., Bailey, R. M., Dunmore, J., Ash, P., Shoraka, S., Zlatkovic, J., Eckman, C. B., et al. (2007) · Journal of Clinical Investigation · doi:10.1172/jci29715 · Cited by 642
Tau fragmentation, aggregation and clearance: the dual role of lysosomal processing
Wang, Y., Martinez-Vicente, M., Krüger, U., Kaushik, S., Wong, E., Mandelkow, E.-M., Cuervo, A. M., & Mandelkow, E. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp367 · Cited by 617
Autophagy failure in Alzheimer's disease—locating the primary defect
Nixon, R. A., & Yang, D.-S. (2011) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.01.021 · Cited by 595
Selective inhibition of Alzheimer disease-like tau aggregation by phenothiazines.
Wischik, C. M., Edwards, P. C., Lai, R. Y., Roth, M., & Harrington, C. R. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.20.11213 · Cited by 547
Murrow, L. M., & Debnath, J. (2012) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathol-020712-163918 · Cited by 546
Proteasome inhibition by paired helical filament‐tau in brains of patients with Alzheimer's disease
Keck, S., Nitsch, R., Grune, T., & Ullrich, O. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.01642.x · Cited by 483
Yang, D.-S., Stavrides, P., Mohan, P. S., Kaushik, S., Kumar, A., Ohno, M., Schmidt, S. D., Wesson, D., Bandyopadhyay, U., Jiang, Y., et al. (2011) · Brain · doi:10.1093/brain/awq341 · Cited by 429
Mechanisms of chaperone-mediated autophagy
Majeski, A. E., & Dice, J. F. (2004) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2004.02.013 · Cited by 411
Biology and pathophysiology of the amyloid precursor protein
Zheng, H., & Koo, E. H. (2011) · Molecular Neurodegeneration · doi:10.1186/1750-1326-6-27 · Cited by 374
Salminen, A., Kaarniranta, K., Kauppinen, A., Ojala, J. O., Haapasalo, A., Soininen, H. S., & Hiltunen, M. O. (2013) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2013.06.002 · Cited by 371
Majumder, S., Richardson, A., Strong, R., & Oddo, S. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025416 · Cited by 365
Zhang, X., Li, L., Chen, S., Yang, D., Wang, Y., Zhang, X., Wang, Z., & Le, W. (2011) · Autophagy · doi:10.4161/auto.7.4.14541 · Cited by 364
Caccamo, A., Magrì, A., Medina, D. X., Wisely, E. V., López‐Aranda, M. F., Silva, A. J., & Oddo, S. (2013) · Aging Cell · doi:10.1111/acel.12057 · Cited by 362
Autophagy failure in A lzheimer's disease and the role of defective lysosomal acidification
Wolfe, D. M., Lee, J., Kumar, A. R., Lee, S., Orenstein, S. J., & Nixon, R. A. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12169 · Cited by 360
Cataldo, A., Hamilton, D. J., Barnett, J. L., Paskevich, P. A., & Nixon, R. A. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-01-00186.1996 · Cited by 356
Tau degradation: the ubiquitin-proteasome system versus the autophagy-lysosome system
Lee, M. J., Lee, J. H., & Rubinsztein, D. C. (2013) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2013.03.001 · Cited by 336
Neuronal loss and brain atrophy in mice lacking cathepsins B and L
Felbor, U., Kessler, B., Mothes, W., Goebel, H. H., Ploegh, H. L., Bronson, R. T., & Olsen, B. R. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.112632299 · Cited by 334
Proteasomal degradation of tau protein
David, D. C., Layfield, R., Serpell, L., Narain, Y., Goedert, M., & Spillantini, M. G. (2002) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2002.01137.x · Cited by 327
Nrf2 reduces levels of phosphorylated tau protein by inducing autophagy adaptor protein NDP52
Jo, C., Gundemir, S., Pritchard, S., Jin, Y. N., Rahman, I., & Johnson, G. V. W. (2014) · Nature Communications · doi:10.1038/ncomms4496 · Cited by 323
Self-citationModeling ALS with iPSCs reveals that mutant SOD1 misregulates neurofilament balance in motor neurons
Chen, H., Qian, K., Du, Z., Cao, J., Petersen, A., Liu, H., Blackbourn, L. W., Huang, C.-L., Errigo, A., Yin, Y., et al. (2014) · Cell stem cell · doi:10.1016/j.stem.2014.02.004 · Cited by 318
Regulation of autophagy by the inositol trisphosphate receptor
Criollo, A., Maiuri, M. C., Tasdemir, E., Vitale, I., Fiebig, A. A., Andrews, D. W., Molgó, J., Dı́az, J., Lavandero, S., Harper, F., et al. (2007) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4402099 · Cited by 312
Tumbarello, D. A., Waxse, B. J., Arden, S. D., Bright, N. A., Kendrick-Jones, J., & Buss, F. (2012) · Nature Cell Biology · doi:10.1038/ncb2589 · Cited by 301
Autophagic degradation of tau in primary neurons and its enhancement by trehalose
Krüger, U., Wang, Y., Kumar, S., & Mandelkow, E.-M. (2012) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.11.009 · Cited by 297
Congdon, E. E., Wu, J. W., Myeku, N., Figueroa, Y. H., Herman, M., Marinec, P. S., Gestwicki, J. E., Dickey, C. A., Yu, W. H., & Duff, K. E. (2012) · Autophagy · doi:10.4161/auto.19048 · Cited by 297
Hamano, T., Gendron, T. F., Causevic, E., Yen, S., Lin, W., Isidoro, C., DeTure, M., & Ko, L. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06084.x · Cited by 283
Yu, W. H., Kumar, A., Peterhoff, C., Shapiro Kulnane, L., Uchiyama, Y., Lamb, B. T., Cuervo, A. M., & Nixon, R. A. (2004) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2004.05.010 · Cited by 279
Luo, W., Dou, F., Rodina, A., Chip, S., Kim, J., Zhao, Q., Moulick, K., Aguirre, J., Wu, N. F., Greengard, P., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0701055104 · Cited by 274
Pickford, F., Masliah, E., Britschgi, M., Lucin, K., Narasimhan, R., Jaeger, P. A., Small, S., Spencer, B., Rockenstein, E., Levine, B., et al. (2008) · Journal of Clinical Investigation · doi:10.1172/jci33585 · Cited by 268
Self-citationZKSCAN3 Is a Master Transcriptional Repressor of Autophagy
Chauhan, S., Goodwin, J. G., Chauhan, S., Manyam, G., Wang, J., Kamat, A. M., & Boyd, D. D. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.01.024 · Cited by 266
Selective degradation of p62 by autophagy
Ichimura, Y., & Komatsu, M. (2010) · Seminars in Immunopathology · doi:10.1007/s00281-010-0220-1 · Cited by 250
Shin, J. Y., Park, H. J., Kim, H. N., Oh, S. H., Bae, J.-S., Ha, H.-J., & Lee, P. H. (2014) · Autophagy · doi:10.4161/auto.26508 · Cited by 243
Chemical Manipulation of Hsp70 ATPase Activity Regulates Tau Stability
Jinwal, U. K., Miyata, Y., Koren, J., Jones, J. R., Trotter, J. H., Chang, L., O’Leary, J. C., Morgan, D., Lee, D. C., Shults, C. L., et al. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3345-09.2009 · Cited by 233
Tau clearance mechanisms and their possible role in the pathogenesis of Alzheimer disease.
Chesser, A. S., Pritchard, S. M., & Johnson, G. V. W. (2013) · Frontiers in Neurology · doi:10.3389/fneur.2013.00122 · Cited by 219
Self-citationChaperone-mediated autophagy at a glance
Kaushik, S., Bandyopadhyay, U., Sridhar, S., Kiffin, R., Martínez‐Vicente, M., Kon, M., Orenstein, S. J., Wong, E. S. P., & Cuervo, A. M. (2011) · Journal of Cell Science · doi:10.1242/jcs.073874 · Cited by 219
Cadmium-induced autophagy and apoptosis are mediated by a calcium signaling pathway
Wang, S. H., Shih, Y. L., Ko, W. C., Wei, Y. H., & Shih, C. M. (2008) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-008-8383-9 · Cited by 217
Methylene Blue Inhibits Amyloid Aβ Oligomerization by Promoting Fibrillization
Necula, M., Breydo, L., Milton, S., Kayed, R., van der Veer, W. E., Tone, P., & Glabe, C. G. (2007) · Biochemistry · doi:10.1021/bi700411k · Cited by 213
Regulation of Amyloid Precursor Protein Processing by the Beclin 1 Complex
Jaeger, P. A., Pickford, F., Sun, C.-H. J., Lucin, K. M., Masliah, E., & Wyss‐Coray, T. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011102 · Cited by 208
Self-citationZhu, Z., Yan, J., Jiang, W., Yao, X., Chen, J., Chen, L., Li, C., Hu, L., Jiang, H., & Shen, X. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4790-12.2013 · Cited by 207
Medina, D. X., Caccamo, A., & Oddo, S. (2010) · Brain Pathology · doi:10.1111/j.1750-3639.2010.00430.x · Cited by 200
Bejarano, E., & Cuervo, A. M. (2010) · Proceedings of the American Thoracic Society · doi:10.1513/pats.200909-102js · Cited by 200
Roles of AMP-activated Protein Kinase in Alzheimer’s Disease
Cai, Z., Yan, L., Li, K., Quazi, S. H., & Zhao, B. (2012) · NeuroMolecular Medicine · doi:10.1007/s12017-012-8173-2 · Cited by 198
Kaminskyy, V. O., & Zhivotovsky, B. (2011) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2011.05.013 · Cited by 193
Coffey, E. E., Beckel, J. M., Laties, A. M., & Mitchell, C. H. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.01.001 · Cited by 191
O’Leary, J. C., Li, Q., Marinec, P. S., Blair, L. J., Congdon, E. E., Johnson, A. G., Jinwal, U. K., Koren, J., Jones, J. R., Kraft, C., et al. (2010) · Molecular Neurodegeneration · doi:10.1186/1750-1326-5-45 · Cited by 180
Esselens, C. W., Oorschot, V. M. J., Baert, V., Raemaekers, T., Spittaels, K., Serneels, L., Zheng, H., Säftig, P., Strooper, B. D., Klumperman, J., et al. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200406060 · Cited by 170
Yang, H., Xie, Z., Wei, L. F., Yang, H. N., Yang, S. N., Zhu, Z., Wang, P., Zhao, C., & Bi, J. Z. (2013) · Stem Cell Research & Therapy · doi:10.1186/scrt227 · Cited by 167
A Caspase Cleaved Form of Tau Is Preferentially Degraded through the Autophagy Pathway
Dolan, P. J., & Johnson, G. V. W. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.110940 · Cited by 147
Self-citationAMPK-independent induction of autophagy by cytosolic Ca2+ increase
Grotemeier, A., Alers, S., Pfisterer, S. G., Paasch, F., Daubrawa, M., Dieterle, A., Viollet, B., Wesselborg, S., Proikas-Cezanne, T., & Stork, B. (2010) · Cellular Signalling · doi:10.1016/j.cellsig.2010.01.015 · Cited by 143
Aβ-induced formation of autophagosomes is mediated by RAGE-CaMKKβ-AMPK signaling
Son, S. M., Jung, E. S., Shin, H. J., Byun, J., & Mook‐Jung, I. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.09.039 · Cited by 142
Localization of sequence variations in PGC-1α influence their modifying effect in Huntington disease
Hong Van, B., Metzger, S., Portal, E., Deyle, C., Rieß, O., & Nguyen, H. P. (2011) · Molecular Neurodegeneration · doi:10.1186/1750-1326-6-1 · Cited by 136
Neely, K. M., Green, K. N., & LaFerla, F. M. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.5156-10.2010 · Cited by 134
Dou, Z., Pan, J.-A., Dbouk, H. A., Ballou, L. M., DeLeon, J. L., Fan, Y., Chen, J.-S., Liang, Z., Li, G., Backer, J., et al. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.01.022 · Cited by 134
Autophagy deregulation in neurodegenerative diseases – recent advances and future perspectives
Cheung, Z. H., & Ip, N. Y. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07314.x · Cited by 131
Zhang, X., Garbett, K., Veeraraghavalu, K., Wilburn, B., Gilmore, R., Mirnics, K., & Sisodia, S. S. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0556-12.2012 · Cited by 122
Wischik, C. M., Bentham, P., Wischik, D., & Seng, K. M. (2008) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2008.05.438 · Cited by 118
Mitochondrial Ca2+ signals in autophagy
Cárdenas, C., & Foskett, J. K. (2012) · Cell Calcium · doi:10.1016/j.ceca.2012.03.001 · Cited by 116
Steele, J., Lachenmayer, M. L., Ju, S., Stock, A., Liken, J., Kim, S. H., Delgado, L. M., Alfaro, I. E., Bernales, S., Verdile, G., et al. (2012) · Molecular Psychiatry · doi:10.1038/mp.2012.106 · Cited by 115
mTOR-Controlled Autophagy Requires Intracellular Ca2+ Signaling
Decuypere, J.-P., Kindt, D., Luyten, T., Welkenhuyzen, K., Missiaen, L., SMEDT, H. D., Bultynck, G., & Parys, J. B. (2013) · PLoS ONE · doi:10.1371/journal.pone.0061020 · Cited by 113
Wilson, C., Murphy, D. D., Giasson, B. I., Zhang, B., Trojanowski, J. Q., & Lee, V. M. ‐. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200403061 · Cited by 108
Autophagy: A double-edged sword in Alzheimer’s disease
Tung, Y.-T., Wang, B., Hu, M., Hsu, W., Lee, H., Huang, W., & Liao, Y. (2012) · Journal of Biosciences · doi:10.1007/s12038-011-9176-0 · Cited by 105
Rapamycin, Autophagy, and Alzheimer's Disease.
Cai, Z., & Yan, L. (2013) · PubMed · Cited by 97
Stimulation of autophagy is neuroprotective in a mouse model of human tauopathy
Schaeffer, V., & Goedert, M. (2012) · Autophagy · doi:10.4161/auto.21488 · Cited by 95
Role of Inositol Trisphosphate Receptors in Autophagy in DT40 Cells
Khan, M. T. M., & Joseph, S. K. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.114207 · Cited by 94
Inomata, M., Niida, S., Shibata, K., & Into, T. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0819-y · Cited by 94
Wang, Y., Martinez-Vicente, M., Krüger, U., Kaushik, S., Wong, E., Mandelkow, E.-M., Cuervo, A. M., & Mandelkow, E. (2010) · Autophagy · doi:10.4161/auto.6.1.10815 · Cited by 90
The Role of Wnt Signaling in the Development of Alzheimer’s Disease: A Potential Therapeutic Target?
Wan, W., Xia, S., Kalionis, B., Liu, L., & Li, Y. (2014) · BioMed Research International · doi:10.1155/2014/301575 · Cited by 86
Dobrowolski, R., Vick, P., Ploper, D., Gumper, I., Snitkin, H., Sabatini, D. D., & Robertis, E. M. D. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.09.026 · Cited by 83
Autophagy Dysfunction in Alzheimer’s Disease
Li, L., Zhang, X., & Le, W. (2010) · Neurodegenerative Diseases · doi:10.1159/000276710 · Cited by 81
Hayashi, S.-I., Sato, N., Yamamoto, A., Ikegame, Y., Nakashima, S., Ogihara, T., & Morishita, R. (2009) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.109.188516 · Cited by 79
Microtubule-associated protein tau is a substrate of ATP/Mg2+-dependent proteasome protease system
Zhang, J. Y., Liu, S. J., Li, H., & Wang, J. (2004) · Journal of Neural Transmission · doi:10.1007/s00702-004-0196-x · Cited by 75
Kajiwara, Y., Franciosi, S., Takahashi, N., Krug, L., Schmeidler, J., Taddei, K., Haroutunian, V. H., Fried, U., Ehrlich, M. E., Martins, R. N., et al. (2010) · Molecular Neurodegeneration · doi:10.1186/1750-1326-5-1 · Cited by 72
ULK1, Mammalian Target of Rapamycin, and Mitochondria: Linking Nutrient Availability and Autophagy
Kundu, M. (2011) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3809 · Cited by 48
Darlington, D., Deng, J., Giunta, B. N., Hou, H., Sanberg, C. D., Kuzmin‐Nichols, N., Zhou, H., Mori, T., Ehrhart, J. C., Sanberg, P. R., et al. (2012) · Stem Cells and Development · doi:10.1089/scd.2012.0345 · Cited by 46
Autophagy takes an alternative pathway
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Mitochondrial Complex Enzyme Activities and Cytochrome c Expression Changes in Multiple Sclerosis
Iñarrea, P., Alarcia, R., Álava, M. A., Capablo, J. L., Casanova, A., Íñiguez, C., Iturralde, M., Larrodé, P., Martín, J., Mostacero, E., et al. (2013) · Molecular Neurobiology · doi:10.1007/s12035-013-8481-z · Cited by 29
Harrington, C. R., Rickard, J. E., Horsley, D., Harrington, K. A., Hindley, K. P., Riedel, G., Theuring, F., Seng, K. M., & Wischik, C. M. (2008) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2008.05.259 · Cited by 21
New Modularity of DAP-Kinases: Alternative Splicing of the DRP-1 Gene Produces a ZIPk-Like Isoform
Shoval, Y., Berissi, H., Kimchi, A., & Pietrokovski, S. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017344 · Cited by 19
PKD at the crossroads of necrosis and autophagy
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HSPCs Get Their Motors Running for Asymmetric Fate Choice
Zheng, Y., & Geiger, H. (2014) · Cell stem cell · doi:10.1016/j.stem.2013.12.002 · Cited by 18
Presenilin-1 Regulates the Expression of p62 to Govern p62-dependent Tau Degradation
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Phase III CONCERT Trial of Latrepirdine
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AMP kinase: the missing link between type 2 diabetes and neurodegenerative diseases?
Kodiha, M., & Stochaj, U. (2011) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2011.07.001 · Cited by 9
Esposito, S. (1964) · Cellular and Molecular Life Sciences · doi:10.1007/bf02151243 · Cited by 5
Research works printed but not linked: 104
- Cai, 2013, Alzheimer disease, autophagy Biochem Pharmacol Res, 1
- Dou, 2013, Class PI β subunit promotes autophagy through in response to growth factor limitation, Small Mol Cell, 50, 110
- Bejarano, 2010, Chaperone mediated Thoracic, autophagy Proc Am Soc, 7
- Cai, 2013, Alzheimer disease, autophagy Biochem Pharmacol Res, 1
- Dou, 2013, Class PI β subunit promotes autophagy through in response to growth factor limitation, Small Mol Cell, 50, 110
- Pankiv, 2007, binds directly to to facilitate degradation of ubiquitinated protein aggregates by autophagy, Biol Chem, 1
- Kaushik, 2011, Chaperone - mediated autophagy at a glance, Cell Sci, 124
- Wischik, 2008, τ aggregation inhibitor therapy with rember arrests disease progression in mild and moderate Alzheimer s disease over weeks Alzheimer, Dementia, 04
- Keck, 2003, Proteasome inhibition by paired helical filament - τ in brains of patients with Alzheimer s disease, Neurochem, 85
- Caccamo, 2013, mTOR regulates τ phosphorylation and degradation : implications for Alzheimer s disease and other tauopathies, Aging Cell, 12, 370, 10.1111/acel.12057 · DOI · Paper page
- Fred Dice, 1990, Peptide sequences that target cytosolic proteins for lysosomal proteolysis Trends, Biochem Sci, 15, 305, 10.1016/0968-0004(90)90019-8 · DOI
- Petrucelli, 2004, CHIP regulate τ ubiquitination degradation aggregation, Hum Mol Genet, 13, 703, 10.1093/hmg/ddh083 · DOI · Paper page
- Wilson, 2004, Degradative organelles containing mislocalized α - and β - synuclein proliferate in presenilin null neurons, Cell Biol, 1
- Nishida, 2009, Discovery of independent alternative macroautophagy, Nature, 461
- Boland, 2008, induction and autophagosome clearance in neurons : relationship to autophagic pathology in Alzheimer s disease, Autophagy Neurosci, 28, 6926
- Tumbarello, 2012, receptors link myosin VI to autophagosomes to mediate Tom - dependent autophagosome maturation and fusion with the lysosome, Autophagy Nat Cell Biol, 14, 1
- Nishida, 2009, Discovery of independent alternative macroautophagy, Nature, 461
- Grotemeier, 2010, independent induction of autophagy by cytosolic Ca increase, Cell Signal, 22, 914, 10.1016/j.cellsig.2010.01.015 · DOI · Paper page
- Stefanis, 2012, α in s disease Cold a, Parkinson Perspect Med, 009399
- Zheng, 2011, Biology and pathophysiology of the amyloid precursor protein, Mol Neurodegener, 6, 1, 10.1186/1750-1326-6-27 · DOI
- Darlington, 2012, Multiple low - dose infusions of human umbilical cord blood cells improve cognitive impairments and reduce amyloid - β - associated neuropathology in Alzheimer mice, Stem Cells Dev, 22, 412, 10.1089/scd.2012.0345 · DOI
- Coffey, 2014, alkalization and dysfunction in human fibroblasts with the Alzheimer s disease - linked presenilin mutation can be reversed with cAMP, Neuroscience, 1
- Querfurth, 2010, Alzheimer disease, Engl J Med, 362
- Zhang, 2005, Microtubule - associated protein τ is a substrate of ATP - dependent proteasome protease system, Neural Transm, 112
- Felbor, 2002, Neuronal loss and brain atrophy in mice lacking cathepsins, Proc Natl Acad Sci USA, 99
- Wang, 2009, τ fragmentation aggregation clearance the dual role of lysosomal processing, Hum Mol Genet, 18, 4153, 10.1093/hmg/ddp367 · DOI · Paper page
- Kirkin, 2009, a role for in autophagosomal degradation of ubiquitinated substrates, Mol Cell, 1
- Hosokawa, 2009, Nutrient - dependent mTORC association with the ULK complex required for, autophagy Mol Biol Cell, 20, 1
- Kundu, 2011, ULK mammalian target of rapamycin mitochondria linking nutrient availability and Antioxidants Signal, autophagy, 14, 1
- Steele, 2013, improves cognition and arrests progression of neuropathology in an Alzheimer s mouse model, Mol Psychiatry, 18, 889, 10.1038/mp.2012.106 · DOI
- Jisun, 2012, mitochondria oxidative stress cross talk redox signalling, Autophagy Biochem J, 441
- Yu, 2004, Autophagic vacuoles are enriched in amyloid precursor protein - secretase activities : implications for β - amyloid peptide over - production and localization in Alzheimer s disease, Int J Biochem Cell Biol, 2531, 10.1016/j.biocel.2004.05.010 · DOI · Paper page
- Salminen, 2013, Impaired processing in Alzheimer s disease : the potential role of interactome, autophagy Prog Neurobiol, 1
- Son, 2012, induced formation of autophagosomes is mediated by RAGE signaling, Aging, 1006
- Yu, 2005, Macroautophagy a novel β - amyloid peptide - generating pathway activated in Alzheimer s disease, Cell Biol, 171
- Bejarano, 2010, Chaperone mediated Thoracic, autophagy Proc Am Soc, 7
- David, 2002, degradation of τ protein, J Neurochem, 176, 10.1046/j.1471-4159.2002.01137.x · DOI · Paper page
- Hosokawa, 2009, Nutrient - dependent mTORC association with the ULK complex required for, autophagy Mol Biol Cell, 20, 1
- Harrington, 2008, Methylthioninium chloride acts as a τ aggregation inhibitor in a cellular model and reverses τ pathology in transgenic mice models of Alzheimer s disease International Conference on Alzheimer s Disease Abstracts
- Wischik, 2008, τ aggregation inhibitor therapy with rember arrests disease progression in mild and moderate Alzheimer s disease over weeks Alzheimer, Dementia, 04
- Wang, 2008, Cadmium - induced autophagy and apoptosis are mediated by a calcium signaling pathway, Cell Mol Life Sci, 3640, 10.1007/s00018-008-8383-9 · DOI
- Necula, 2007, Der Veer Methylene blue inhibits amyloid Aβ oligomerization by promoting fibrillization, Biochemistry Moscow, 8850, 10.1021/bi700411k · DOI · Paper page
- Harrington, 2008, Methylthioninium chloride acts as a τ aggregation inhibitor in a cellular model and reverses τ pathology in transgenic mice models of Alzheimer s disease International Conference on Alzheimer s Disease Abstracts
- Martina, 2014, and The nutrient - responsive transcription factor promotes autophagy lysosomal biogenesis and clearance of cellular debris Signal ra, Sci
- Cataldo, 1996, Properties of the endosomal - lysosomal system in the human central nervous system : disturbances mark most neurons in populations at risk to degenerate in Alzheimer s disease, Neurosci, 16, 186, 10.1523/JNEUROSCI.16-01-00186.1996 · DOI
- Kodiha, 2011, AMP kinase the missing link between type diabetes and neurodegenerative diseases Trends, Mol Med, 17, 613
- Nixon, 2011, failure in Alzheimer s disease locating the primary defect, Autophagy Dis, 43, 38
- Johansen, 2011, Selective autophagy mediated by autophagic adapter proteins, Autophagy, 279, 10.4161/auto.7.3.14487 · DOI
- Chen, 2014, IV Modeling ALS with iPSCs reveals that mutant SOD misregulates neurofilament balance in motor neurons, Cell Stem Cell, 14, 1, 10.1016/j.stem.2014.02.004 · DOI · Paper page
- Li, 2012, lesser known self eating, Cell Mol Life Sci, 69
- Jinwal, 2009, rd Chemical manipulation of hsp activity regulates τ stability, Neurosci, 29, 12079, 10.1523/JNEUROSCI.3345-09.2009 · DOI
- Bjørkøy, 2005, forms protein aggregates degraded by autophagy and has a protective effect on huntingtin - induced cell death, Cell Biol, 1
- Scheff, 2006, Hippocampal synaptic loss in early Alzheimer s disease and mild cognitive impairment, Aging, 27, 1372
- Shimizu, 2010, takes an alternative pathway, Autophagy Autophagy, 290, 10.4161/auto.6.2.11127 · DOI
- Kim, 2002, mTOR interacts with raptor to form a nutrient - sensitive complex that signals to the cell growth machinery, Cell, 110
- Tung, 2012, a double - edged sword in Alzheimer s disease, Autophagy, 37
- Khan, 2010, Role of inositol trisphosphate receptors in autophagy in cells, Biol Chem, 285
- Zhu, 2013, Arctigenin effectively ameliorates memory impairment in Alzheimer s disease model mice targeting both β - amyloid production and clearance, Neurosci, 13138, 10.1523/JNEUROSCI.4790-12.2013 · DOI
- Hamano, 2008, Autophagic - lysosomal perturbation enhances τ aggregation in transfectants with induced wild - type τ expression, Eur J Neurosci, 27, 1119, 10.1111/j.1460-9568.2008.06084.x · DOI · Paper page
- Vingtdeux, 2010, AMP - activated protein kinase signaling activation by resveratrol modulates amyloid - β peptide metabolism, Biol Chem, 285
- Ichimura, 2010, Selective degradation of by, autophagy Immunopathol, 431
- Majeski, 2004, Mechanisms of chaperone mediated, autophagy Int J Biochem Cell Biol, 2435, 10.1016/j.biocel.2004.02.013 · DOI
- Rubinsztein, 2006, The roles of intracellular protein - degradation pathways in neurodegeneration, Nature, 443
- Krüger, 2012, Autophagic degradation of τ in primary neurons and its enhancement by trehalose, Aging, 2291
- Wan, 2014, The role of Wnt signaling in the development of Alzheimer s disease : a potential therapeutic target, Res Int
- Criollo, 2007, Regulation of autophagy by the inositol trisphosphate receptor, Cell Death Differ, 14, 1029, 10.1038/sj.cdd.4402099 · DOI
- Berger, 2006, Rapamycin alleviates toxicity of different aggregate - prone proteins, Hum Mol Genet, 15, 433, 10.1093/hmg/ddi458 · DOI · Paper page
- Dickey, 2007, The high - affinity CHIP complex recognizes and selectively degrades phosphorylated τ client proteins, Clin Invest, 117
- Hayashi, 2009, Alzheimer disease - associated peptide β inhibits vascular regeneration with induction of endothelial autophagy, amyloid Thromb Biol, 29, 1909, 10.1161/ATVBAHA.109.188516 · DOI
- Cai, 2012, Roles of AMP - activated protein kinase in Alzheimer s disease, Med, 14, 1
- Sarkar, 2007, a novel mTOR - independent autophagy enhancer accelerates the clearance of mutant huntingtin and α - synuclein, Biol Chem, 282
- Jo, 2014, reduces levels of phosphorylated τ protein by inducing autophagy adaptor protein, Nat Commun, 3496, 10.1038/ncomms4496 · DOI · Paper page
- Kaminskyy, 2012, Proteases in Proteins, autophagy Biochim Biophys Acta Proteomics, 44, 10.1016/j.bbapap.2011.05.013 · DOI
- Sweetlove, 2012, Phase III CONCERT trial of latrepirdine, Pharm Med, 26, 113, 10.1007/BF03256900 · DOI
- Leary, 2010, rd rd - mediated rescue of cognition in τ transgenic mice requires neuroprotection and reduced soluble τ burden, Mol Neurodegener, 5, 1, 10.1186/1750-1326-5-45 · DOI
- Neely, 2011, Presenilin is necessary for efficient proteolysis through the autophagy - lysosome system in a γ - secretase - independent manner, Neurosci, 31, 2781, 10.1523/JNEUROSCI.5156-10.2010 · DOI · Paper page
- Sancak, 2010, Bar - Rag complex targets mTORC to the lysosomal surface and is necessary for its activation by amino acids, Cell, 1
- Son, 2012, induced formation of autophagosomes is mediated by RAGE signaling, Aging, 1006
- Chauhan, 2013, is a master transcriptional repressor of, autophagy Mol Cell, 50, 16, 10.1016/j.molcel.2013.01.024 · DOI · Paper page
- Dobrowolski, 2012, Presenilin deficiency or lysosomal inhibition enhances Wnt signaling through relocalization of to the late - endosomal compartment, Cell Rep, 29, 1316, 10.1016/j.celrep.2012.09.026 · DOI
- Shin, 2014, Mesenchymal stem cells enhance autophagy and increase β - amyloid clearance in Alzheimer disease models, Autophagy, 10
- Caccamo, 2010, Molecular interplay between mammalian target of rapamycin mTOR β τ effects on cognitive impairments, amyloid Biol Chem, 285
- Yang, 2013, Human umbilical cord mesenchymal stem cell - derived neuron - like cells rescue memory deficits and reduce amyloid - β deposition in an AβPP transgenic mouse model, PS Cell Res Ther, 1
- Pankiv, 2007, binds directly to to facilitate degradation of ubiquitinated protein aggregates by autophagy, Biol Chem, 1
- Lee, 2010, proteolysis and autophagy require presenilin are disrupted by Alzheimer - related mutations, PS Cell, 1
- Esselens, 2004, mediates the turnover of telencephalin in hippocampal neurons via an autophagic degradative pathway, Cell Biol, 1
- Zhang, 2012, role for presenilins in autophagy revisited : normal acidification of lysosomes in cells lacking, Neurosci, 8633, 10.1523/JNEUROSCI.0556-12.2012 · DOI · Paper page
- Li, 2010, dysfunction in Alzheimer s disease, Autophagy Dis, 265
- Querfurth, 2010, Alzheimer disease, Engl J Med, 362
- Pickford, 2008, The autophagy - related protein shows reduced expression in early Alzheimer disease and regulates amyloid β accumulation in mice, Clin Invest, 1
- Medina, 2011, Methylene blue reduces Aβ levels and rescues early cognitive deficit by increasing proteasome activity, Brain Pathol, 21, 140, 10.1111/j.1750-3639.2010.00430.x · DOI
- Lee, 2013, τ degradation : the ubiquitin - proteasome system versus the autophagy - lysosome system, Prog Neurobiol, 105
- Zhang, 2011, Rapamycin treatment augments motor neuron degeneration in SOD mouse model of amyotrophic lateral sclerosis, Autophagy, 1
- Wischik, 1996, Selective inhibition of Alzheimer disease - like τ aggregation by phenothiazines, Proc Natl Acad Sci USA, 11213, 10.1073/pnas.93.20.11213 · DOI · Paper page
- Tung, 2014, regulates the expression of to govern - dependent τ degradation, Mol Neurobiol, 49, 1, 10.1007/s12035-013-8482-y · DOI
- Dolan, 2010, caspase cleaved form of τ is preferentially degraded through the autophagy pathway, Biol Chem, 285
- Cárdenas, 2012, Mitochondrial Ca signals in, autophagy Cell Calcium, 52, 44, 10.1016/j.ceca.2012.03.001 · DOI
- Dekosky, 1990, loss in frontal cortex biopsies in Alzheimer s disease : correlation with cognitive severity, Synapse Ann Neurol, 27, 457, 10.1002/ana.410270502 · DOI · Paper page
- Settembre, 2011, links autophagy to lysosomal biogenesis, Science, 332
- Cheung, 2011, Ip deregulation in neurodegenerative diseases recent advances and future perspectives, Autophagy Neurochem, 317, 10.1111/j.1471-4159.2011.07314.x · DOI
- Inomata, 2012, Into Regulation of Toll - like receptor signaling by mediated selective autophagy is normally inactivated by, Cell Mol Life Sci, 20, 69
- Chapman, 1999, Impaired synaptic plasticity and learning in aged amyloid precursor protein transgenic mice, Nat Neurosci, 271, 10.1038/6374 · DOI · Paper page
- Luo, 2007, Roles of heat - shock protein in maintaining and facilitating the neurodegenerative phenotype in tauopathies, Proc Natl Acad Sci USA, 9511, 10.1073/pnas.0701055104 · DOI
- Kirkin, 2009, role for ubiquitin in selective, autophagy Mol Cell, 259, 10.1016/j.molcel.2009.04.026 · DOI
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“This is supported by a number of studies reporting dysregulation in many autophagic/lysosomal pathways in the context of AD [234,235], while the vast majority of AD-associated genes appears to be related to these same pathways [232].”
BackgroundMachine learning identifies candidates for drug repurposing in Alzheimer’s disease
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Metadata
- Authors
- Zare-shahabadi, A., Masliah, E., Johnson, G. V. W., & Rezaei, N.
- Affiliations
- Tehran University of Medical Sciences (IR)
- University of California San Diego (US)
- University of Rochester Medicine (US)
- Universal Scientific Education and Research Network (IR)
- Corresponding author
- Rezaei, Nima
- Venue
- Reviews in the Neurosciences
- Publisher
- Walter de Gruyter GmbH
- Published
- 2015-01-01
- Volume
- 26
- Issue
- 4
- Pages
- 385-95
- ISSN
- 0334-1763 (ISSN-L)
- 2191-0200
- PMC
- PMC5039008
- OpenAlex
- W1992935533
- Cited by
- 204
- References
- 119
- Citations by year
- 2026: 2 · 2025: 10 · 2024: 10 · 2023: 21 · 2022: 27 · 2021: 25 · 2020: 38 · 2019: 27 · 2018: 21 · 2017: 19 · 2016: 3 · 2015: 1
- FWCI
- 1.89
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Reviews in the Neurosciences (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute on Aging (R01AG018440)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- autophagy, Alzheimer's disease, autophagy-lysosome pathway, neurodegeneration, proteostasis, neuronal survival, lysosomal dysfunction
- MeSH terms
- Alzheimer Disease, Animals, Autophagy, Humans, Amyloid beta-Peptides, tau Proteins
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