A Becn1 mutation mediates hyperactive autophagic sequestration of amyloid oligomers and improved cognition in Alzheimer's disease
Open accessAbstract
Impairment of the autophagy pathway has been observed during the pathogenesis of Alzheimer's disease (AD), a neurodegenerative disorder characterized by abnormal deposition of extracellular and intracellular amyloid β (Aβ) peptides. Yet the role of autophagy in Aβ production and AD progression is complex. To study whether increased basal autophagy plays a beneficial role in Aβ clearance and cognitive improvement, we developed a novel genetic model to hyperactivate autophagy in vivo. We found that knock-in of a point mutation F121A in the essential autophagy gene Beclin 1/Becn1 in mice significantly reduces the interaction of BECN1 with its inhibitor BCL2, and thus leads to constitutively active autophagy even under non-autophagy-inducing conditions in multiple tissues, including brain. Becn1F121A-mediated autophagy hyperactivation significantly decreases amyloid accumulation, prevents cognitive decline, and restores survival in AD mouse models. Using an immunoisolation method, we found biochemically that Aβ oligomers are autophagic substrates and sequestered inside autophagosomes in the brain of autophagy-hyperactive AD mice. In addition to genetic activation of autophagy by Becn1 gain-of-function, we also found that ML246, a small-molecule autophagy inducer, as well as voluntary exercise, a physiological autophagy inducer, exert similar Becn1-dependent protective effects on Aβ removal and memory in AD mice. Taken together, these results demonstrate that genetically disrupting BECN1-BCL2 binding hyperactivates autophagy in vivo, which sequestrates amyloid oligomers and prevents AD progression. The study establishes new approaches to activate autophagy in the brain, and reveals the important function of Becn1-mediated autophagy hyperactivation in the prevention of AD.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
When autophagy is impaired, Aβ peptides can accumulate intracellularly while their extracellular release decreases.
“Evidence indicates that Aβ peptides can accumulate intracellularly while their extracellular release decreases when autophagy is impaired [85, 93].”
From Senescence-related impairment of autophagy induces toxic intraneuronal amyloid-β accumulation in a mouse model of amyloid pathology (2023) · cites this paper as [93]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
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 · see citing works
Genome engineering using the CRISPR-Cas9 system
Ran, F. A., Hsu, P. D., Wright, J., Agarwala, V., Scott, D. A., & Zhang, F. (2013) · Nature Protocols · doi:10.1038/nprot.2013.143 · Cited by 11,133 · see citing works
Sperling, R. A., Aisen, P. S., Beckett, L. A., Bennett, D. A., Craft, S., Fagan, A. M., Iwatsubo, T., Jack, C. R., Kaye, J., Montine, T. J., et al. (2011) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2011.03.003 · Cited by 7,155 · see citing works
Autophagy: Renovation of Cells and Tissues
Mizushima, N., & Komatsu, M. (2011) · Cell · doi:10.1016/j.cell.2011.10.026 · Cited by 6,467 · see citing works
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 · see citing works
Exercise training increases size of hippocampus and improves memory
Erickson, K. I., Voss, M. W., Prakash, R. S., Basak, C., Szabo, A., Chaddock, L., Kim, J. S., Heo, S., Alves, H., White, S. M., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1015950108 · Cited by 4,855 · see citing works
Suppression of basal autophagy in neural cells causes neurodegenerative disease in mice
Hara, T., Nakamura, K., Matsui, M., Yamamoto, A., Nakahara, Y., Suzuki-Migishima, R., Yokoyama, M., Mishima, K., Saito, I., Okano, H., et al. (2006) · Nature · doi:10.1038/nature04724 · Cited by 3,882 · see citing works
Levine, B., & Klionsky, D. J. (2004) · Developmental Cell · doi:10.1016/s1534-5807(04)00099-1 · Cited by 3,672 · see citing works
Self-citationBcl-2 Antiapoptotic Proteins Inhibit Beclin 1-Dependent Autophagy
Pattingre, S., Tassa, A., Qu, X., Garuti, R., Liang, X. H., Mizushima, N., Packer, M., Schneider, M. D., & Levine, B. (2005) · Cell · doi:10.1016/j.cell.2005.07.002 · Cited by 3,536 · see citing works
Self-citationOakley, H., Cole, S. L., Logan, S., Maus, E., Shao, P., Craft, J., Guillozet-Bongaarts, A., Ohno, M., Disterhoft, J., Van Eldik, L., et al. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.1202-06.2006 · Cited by 3,530 · see citing works
Self-citationLoss of autophagy in the central nervous system causes neurodegeneration in mice
Komatsu, M., Waguri, S., Chiba, T., Murata, S., Iwata, J.-I., Tanida, I., Ueno, T., Koike, M., Uchiyama, Y., Kominami, E., et al. (2006) · Nature · doi:10.1038/nature04723 · Cited by 3,500 · see citing works
de Duve, C., & Wattiaux, R. (1966) · Annual Review of Physiology · doi:10.1146/annurev.ph.28.030166.002251 · Cited by 3,033 · see citing works
Alzheimer-type neuropathology in transgenic mice overexpressing V717F β-amyloid precursor protein
Games, D., Adams, D., Alessandrini, R., Barbour, R., Borthelette, P., Blackwell, C., Carr, T., Clemens, J., Donaldson, T., Gillespie, F., et al. (1995) · Nature · doi:10.1038/373523a0 · Cited by 2,516 · see citing works
Mizushima, N., Yamamoto, A., Matsui, M., Yoshimori, T., & Ohsumi, Y. (2003) · Molecular Biology of the Cell · doi:10.1091/mbc.e03-09-0704 · Cited by 2,323 · see citing works
Promotion of tumorigenesis by heterozygous disruption of the beclin 1 autophagy gene
Qu, X., Yu, J., Bhagat, G., Furuya, N., Hibshoosh, H., Troxel, A., Rosen, J., Eskelinen, E.-L., Mizushima, N., Ohsumi, Y., et al. (2003) · Journal of Clinical Investigation · doi:10.1172/jci20039 · Cited by 2,311 · see citing works
Self-citationAutophagosome formation: core machinery and adaptations
Xie, Z., & Klionsky, D. J. (2007) · Nature Cell Biology · doi:10.1038/ncb1007-1102 · Cited by 2,165 · see citing works
A Century of Alzheimer's Disease
Goedert, M., & Spillantini, M. G. (2006) · Science · doi:10.1126/science.1132814 · Cited by 2,106 · see citing works
The role of autophagy in neurodegenerative disease
Nixon, R. A. (2013) · Nature Medicine · doi:10.1038/nm.3232 · Cited by 2,059 · see citing works
Intracellular amyloid-β in Alzheimer's disease
LaFerla, F. M., Green, K. N., & Oddo, S. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2168 · Cited by 1,942 · see citing works
Alzheimer Mechanisms and Therapeutic Strategies
Huang, Y., & Mucke, L. (2012) · Cell · doi:10.1016/j.cell.2012.02.040 · Cited by 1,758 · see citing works
Isolation and characterization of autophagy‐defective mutants of Saccharomyces cerevisiae
Tsukada, M., & Ohsumi, Y. (1993) · FEBS Letters · doi:10.1016/0014-5793(93)80398-e · Cited by 1,756 · see citing works
Defeating Alzheimer's disease and other dementias: a priority for European science and society
Winblad, B., Amouyel, P., Andrieu, S., Ballard, C., Brayne, C., Brodaty, H., Cedazo-Minguez, A., Dubois, B., Edvardsson, D., Feldman, H., et al. (2016) · The Lancet Neurology · doi:10.1016/s1474-4422(16)00062-4 · Cited by 1,676 · see citing works
Larson, E. B., Wang, L., Bowen, J. D., McCormick, W. C., Teri, L., Crane, P., & Kukull, W. (2006) · Annals of Internal Medicine · doi:10.7326/0003-4819-144-2-200601170-00004 · Cited by 1,463 · see citing works
Alzheimer’s Disease: The Challenge of the Second Century
Holtzman, D. M., Morris, J. C., & Goate, A. M. (2011) · Science Translational Medicine · doi:10.1126/scitranslmed.3002369 · Cited by 1,424 · see citing works
JNK1-Mediated Phosphorylation of Bcl-2 Regulates Starvation-Induced Autophagy
Wei, Y., Pattingre, S., Sinha, S., Bassik, M., & Levine, B. (2008) · Molecular Cell · doi:10.1016/j.molcel.2008.06.001 · Cited by 1,329 · see citing works
Self-citationExercise-induced BCL2-regulated autophagy is required for muscle glucose homeostasis
He, C., Bassik, M. C., Moresi, V., Sun, K., Wei, Y., Zou, Z., An, Z., Loh, J., Fisher, J., Sun, Q., et al. (2012) · Nature · doi:10.1038/nature10758 · Cited by 1,136 · see citing works
Self-citationTrafficking and Proteolytic Processing of APP
Haass, C., Kaether, C., Thinakaran, G., & Sisodia, S. (2012) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a006270 · Cited by 1,075 · see citing works
Pickford, F., Masliah, E., Britschgi, M., Lucin, K. M., Narasimhan, R., Jaeger, P. A., Small, S. A., Spencer, B. J., Rockenstein, E. M., Levine, B., et al. (2008) · Journal of Clinical Investigation · doi:10.1172/jci33585 · Cited by 1,072 · see citing works
Self-citationSpilman, 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 · see citing works
Physical Activity, Diet, and Risk of Alzheimer Disease
Scarmeas, N. (2009) · JAMA · doi:10.1001/jama.2009.1144 · Cited by 916 · see citing works
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 · see citing works
Voluntary Exercise Decreases Amyloid Load in a Transgenic Model of Alzheimer's Disease
Adlard, P. A., Perreau, V. M., Pop, V., & Cotman, C. W. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0496-05.2005 · Cited by 806 · see citing works
BACE1 is the major β-secretase for generation of Aβ peptides by neurons
Cai, H., Wang, Y.-S., McCarthy, D., Wen, H., Borchelt, D., Price, D. L., & Wong, P. (2001) · Nature Neuroscience · doi:10.1038/85064 · Cited by 791 · see citing works
Self-citationSmall Molecule Inhibition of the Autophagy Kinase ULK1 and Identification of ULK1 Substrates
Egan, D. F., Chun, M. G. H., Vamos, M., Zou, H., Rong, J., Miller, C. J., Lou, H. J., Raveendra-Panickar, D., Yang, C.-C., Sheffler, D. J., et al. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.05.031 · Cited by 715 · see citing works
Takahashi, R. H., Milner, T. A., Li, F., Nam, E. E., Edgar, M. A., Yamaguchi, H., Beal, M. F., Xu, H., Greengard, P., & Gouras, G. K. (2002) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)64463-x · Cited by 706 · see citing works
He, C., & Levine, B. (2010) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2010.01.001 · Cited by 659 · see citing works
Self-citationPhysical activity and memory functions: An interventional study
Ruscheweyh, R., Willemer, C., Krüger, K., Duning, T., Warnecke, T., Sommer, J., Völker, K., Ho, H. V., Mooren, F., Knecht, S., et al. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2009.08.001 · Cited by 499 · see citing works
Aβ Secretion and Plaque Formation Depend on Autophagy
Nilsson, P., Loganathan, K., Sekiguchi, M., Matsuba, Y., Hui, K., Tsubuki, S., Tanaka, M., Iwata, N., Saito, T., & Saido, T. C. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.08.042 · Cited by 459 · see citing works
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 · see citing works
Majumder, S., Richardson, A. G., Strong, R., & Oddo, S. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025416 · Cited by 401 · see citing works
Lucin, K. M., O’Brien, C. E., Bieri, G., Czirr, E., Mosher, K. I., Abbey, R. J., Mastroeni, D. F., Rogers, J., Spencer, B., Masliah, E., et al. (2013) · Neuron · doi:10.1016/j.neuron.2013.06.046 · Cited by 374 · see citing works
Autophagy-mediated clearance of huntingtin aggregates triggered by the insulin-signaling pathway
Yamamoto, A., Cremona, M. L., & Rothman, J. E. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200510065 · Cited by 355 · see citing works
Short-term fasting induces profound neuronal autophagy
Alirezaei, M., Kemball, C. C., Flynn, C. T., Wood, M. R., Whitton, J. L., & Kiosses, W. B. (2010) · Autophagy · doi:10.4161/auto.6.6.12376 · Cited by 310 · see citing works
Preclinical Alzheimer disease—the challenges ahead
Sperling, R. A., Karlawish, J., & Johnson, K. A. (2013) · Nature Reviews Neurology · doi:10.1038/nrneurol.2012.241 · Cited by 291 · see citing works
Grumati, P., Coletto, L., Schiavinato, A., Castagnaro, S., Bertaggia, E., Sandri, M., & Bonaldo, P. (2011) · Autophagy · doi:10.4161/auto.7.12.17877 · Cited by 267 · see citing works
Exercise induces autophagy in peripheral tissues and in the brain
He, C., Sumpter, R., & Levine, B. (2012) · Autophagy · doi:10.4161/auto.21327 · Cited by 259 · see citing works
Self-citationPhysical Exercise Protects Against Alzheimer's Disease in 3xTg-AD Mice
García‐Mesa, Y., López, J. C., Giménez‐Llort, L., Revilla, S., Guerra, R., Gruart, A., LaFerla, F. M., Cristòfol, R. M., Delgado-Garcia, J. M., & Sanfeliu, C. (2011) · Journal of Alzheimer s Disease · doi:10.3233/jad-2011-101635 · Cited by 253 · see citing works
Yuede, C. M., Zimmerman, S., Dong, H., Kling, M. J., Bero, A. W., Holtzman, D. M., Timson, B. F., & Csernansky, J. G. (2009) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.06.002 · Cited by 250 · see citing works
Tian, Y., Chang, J. C., Fan, E. Y., Flajolet, M., & Greengard, P. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1315110110 · Cited by 233 · see citing works
Hurtado, D. E., Molina-Porcel, L., Iba, M., Aboagye, A. K., Paul, S. M., Trojanowski, J. Q., & Lee, V. M.-Y. (2010) · The American Journal of Pathology · doi:10.2353/ajpath.2010.100346 · Cited by 222 · see citing works
Aβ reduction in BACE1 heterozygous null 5XFAD mice is associated with transgenic APP level
Sadleir, K. R., Eimer, W. A., Cole, S. L., & Vassar, R. (2015) · Molecular Neurodegeneration · doi:10.1186/1750-1326-10-1 · Cited by 213 · see citing works
Self-citationRegulation 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 204 · see citing works
Tapia‐Rojas, C., Aránguiz, F. C., Varela‐Nallar, L., & Inestrosa, N. C. (2015) · Brain Pathology · doi:10.1111/bpa.12255 · Cited by 168 · see citing works
Beclin 2 Functions in Autophagy, Degradation of G Protein-Coupled Receptors, and Metabolism
He, C., Wei, Y., Sun, K., Li, B., Dong, X., Zou, Z., Liu, Y., Kinch, L. N., Khan, S., Sinha, S. C., et al. (2013) · Cell · doi:10.1016/j.cell.2013.07.035 · Cited by 150 · see citing works
Self-citationHurtado, D. E., Molina-Porcel, L., Carroll, J. C., MacDonald, C., Aboagye, A. K., Trojanowski, J. Q., & Lee, V. M.-Y. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.0889-12.2012 · Cited by 126 · see citing works
Shibuya, Y., Chang, C. C. Y., Huang, L.-H., Bryleva, E. Y., & Chang, T.-Y. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.2567-14.2014 · Cited by 108 · see citing works
Gao, W., Kang, J. H., Liao, Y., Ding, W.-X., Gambotto, A. A., Watkins, S. C., Liu, Y.-J., Stolz, D. B., & Yin, X.-M. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.054197 · Cited by 94 · see citing works
Macroautophagy Is Not Directly Involved in the Metabolism of Amyloid Precursor Protein
Boland, B., Smith, D. A., Mooney, D., Jung, S. S., Walsh, D. M., & Platt, F. M. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.186411 · Cited by 91 · see citing works
Chen, X., Kondo, K., Motoki, K., Homma, H., & Okazawa, H. (2015) · Scientific Reports · doi:10.1038/srep12115 · Cited by 83 · see citing works
Identification of natural products with neuronal and metabolic benefits through autophagy induction
Fan, Y., Wang, N., Rocchi, A., Zhang, W., Vassar, R. J., Zhou, Y., & He, C. (2016) · Autophagy · doi:10.1080/15548627.2016.1240855 · Cited by 78 · see citing works
Self-citationSUMO1 promotes Aβ production via the modulation of autophagy
Cho, S., Yun, S., Jo, C., Lee, D., Choi, K. J., Song, J. C., Park, S. I., Kim, Y.-J., & Koh, Y. H. (2014) · Autophagy · doi:10.4161/15548627.2014.984283 · Cited by 76 · see citing works
Emerging roles of autophagy in metabolism and metabolic disorders
Rocchi, A., & He, C. (2015) · Frontiers in Biology · doi:10.1007/s11515-015-1354-2 · Cited by 65 · see citing works
Self-citationBECN1/Beclin 1 sorts cell-surface APP/amyloid β precursor protein for lysosomal degradation
Swaminathan, G., Zhu, W., & Plowey, E. D. (2016) · Autophagy · doi:10.1080/15548627.2016.1234561 · Cited by 50 · see citing works
Activating Autophagy by Aerobic Exercise in Mice
Rocchi, A., & He, C. (2017) · Journal of Visualized Experiments · doi:10.3791/55099 · Cited by 39 · see citing works
Self-citationAutophagy activation by novel inducers prevents BECN2-mediated drug tolerance to cannabinoids
Kuramoto, K., Wang, N., Fan, Y., Zhang, W., Schoenen, F. J., Frankowski, K. J., Marugán, J., Zhou, Y., Huang, S., & He, C. (2016) · Autophagy · doi:10.1080/15548627.2016.1187367 · Cited by 19 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Biological Functions of Autophagy Genes: A Disease Perspective
Levine, B., & Kroemer, G. (2019) · Cell · doi:10.1016/j.cell.2018.09.048 · Cited by 2,832 · see citing works
Self-citationAutophagy in healthy aging and disease
Aman, Y., Schmauck-Medina, T., Hansen, M., Morimoto, R. I., Simon, A. K., Bjedov, I., Palikaras, K., Simonsen, A., Johansen, T., Tavernarakis, N., et al. (2021) · Nature Aging · doi:10.1038/s43587-021-00098-4 · Cited by 1,313 · see citing works
The Amyloid-β Oligomer Hypothesis: Beginning of the Third Decade
Cline, E. N., Bicca, M. A., Viola, K. L., & Klein, W. L. (2018) · Journal of Alzheimer's Disease · doi:10.3233/jad-179941 · Cited by 870 · see citing works
Disruption of the beclin 1–BCL2 autophagy regulatory complex promotes longevity in mice
Fernández, Á. F., Sebti, S., Wei, Y., Zou, Z., Shi, M., McMillan, K. L., He, C., Ting, T., Liu, Y., Chiang, W.-C., et al. (2018) · Nature · doi:10.1038/s41586-018-0162-7 · Cited by 630 · see citing works
Self-citationPromoting the clearance of neurotoxic proteins in neurodegenerative disorders of ageing
Boland, B., Yu, W. H., Corti, O., Mollereau, B., Henriques, A., Bézard, E., Pastores, G., Rubinsztein, D. C., Nixon, R. A., Duchen, M. R., et al. (2018) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2018.109 · Cited by 552 · see citing works
Self-citationAutophagy and the cell biology of age-related disease
Leidal, A. M., Levine, B., & Debnath, J. (2018) · Nature Cell Biology · doi:10.1038/s41556-018-0235-8 · Cited by 424 · see citing works
Self-citationAutophagy in Alzheimer’s disease pathogenesis: Therapeutic potential and future perspectives
Zhang, Z., Yang, X., Song, Y., & Tu, J. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101464 · Cited by 378 · see citing works
Beclin 1 Phosphorylation – at the Center of Autophagy Regulation
Menon, M., & Dhamija, S. (2018) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2018.00137 · Cited by 342 · see citing works
Possible Neuroprotective Mechanisms of Physical Exercise in Neurodegeneration
Mahalakshmi, B., Maurya, N., Lee, S., & Kumar, V. B. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21165895 · Cited by 360 · see citing works
Xu, H., & Qin, Z. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-981-15-0602-4_5 · Cited by 318 · see citing works
Role of tau protein in Alzheimer’s disease: The prime pathological player
Muralidar, S., Ambi, S. V., Sekaran, S., Thirumalai, D., & Palaniappan, B. (2020) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2020.07.327 · Cited by 278 · see citing works
Autophagy Induction as a Therapeutic Strategy for Neurodegenerative Diseases
Djajadikerta, A., Keshri, S., Tanasa, M. P., Prestil, R., Ryan, L., & Rubinsztein, D. C. (2019) · Journal of Molecular Biology · doi:10.1016/j.jmb.2019.12.035 · Cited by 238 · see citing works
Dewanjee, S., Chakraborty, P., Bhattacharya, H., Chacko, L., Singh, B., Chaudhary, A., Javvaji, K., Pradhan, S. R., Vallamkondu, J., Dey, A., et al. (2022) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2022.09.032 · Cited by 235 · see citing works
Post-translational modifications of Beclin 1 provide multiple strategies for autophagy regulation
Hill, S. M., Wróbel, L., & Rubinsztein, D. C. (2018) · Cell Death and Differentiation · doi:10.1038/s41418-018-0254-9 · Cited by 221 · see citing works
BECLIN1: Protein Structure, Function and Regulation
Tran, S. H., Fairlie, W. D., & Lee, E. F. (2021) · Cells · doi:10.3390/cells10061522 · Cited by 224 · see citing works
Targeting Autophagy for the Treatment of Alzheimer’s Disease: Challenges and Opportunities
Liu, J., & Li, L. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00203 · Cited by 159 · see citing works
Autophagy Differentially Regulates Insulin Production and Insulin Sensitivity
Yamamoto, S., Kuramoto, K., Wang, N., Situ, X., Priyadarshini, M., Zhang, W., Cordoba-Chacon, J., Layden, B. T., & He, C. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.05.032 · Cited by 144 · see citing works
Self-citationWang, S., Wang, L., Qin, X., Turdi, S., Sun, D., Culver, B., Reiter, R. J., Wang, X., Zhou, H., & Ren, J. (2020) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-020-0171-5 · Cited by 135 · see citing works
Pignataro, P., Dicarlo, M., Zerlotin, R., Zecca, C., Dell’Abate, M. T., Buccoliero, C., Logroscino, G., Colucci, S. C., & Grano, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22041605 · Cited by 131 · see citing works
Increased autophagy blocks HER2-mediated breast tumorigenesis
Vega-Rubín-de-Celis, S., Zou, Z., Fernández, Á. F., Ci, B., Kim, M., Xiao, G., Xie, Y., & Levine, B. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1717800115 · Cited by 129 · see citing works
Self-citationAutophagy in Age-Associated Neurodegeneration
Metaxakis, A., Ploumi, C., & Tavernarakis, N. (2018) · Cells · doi:10.3390/cells7050037 · Cited by 121 · see citing works
The beclin 1 interactome: Modification and roles in the pathology of autophagy-related disorders
Kaur, S., & Changotra, H. (2020) · Biochimie · doi:10.1016/j.biochi.2020.04.025 · Cited by 114 · see citing works
β-cell autophagy: Mechanism and role in β-cell dysfunction
Lee, Y., Kim, J., Park, K., & Lee, M. (2019) · Molecular Metabolism · doi:10.1016/j.molmet.2019.06.014 · Cited by 102 · see citing works
Crosstalk between apoptosis and autophagy signaling pathways
(2020) · International Review of Cell and Molecular Biology · doi:10.1016/bs.ircmb.2020.01.003 · Cited by 92 · see citing works
Targeting autophagy in Alzheimer’s disease: Animal models and mechanisms
Zhang, X.-W., 澳门大学中华医药研究院中药质量研究国家重点实验室, 澳. 凼. 9., State Key Laboratory of Quality Research in Chinese Medicine, I. O. C. M. S., Zhu, X.-X., Tang, D.-S., Lu, J.-H., 佛山大学广东省动物分子设计与精准育种重点实验室, 广., & Guangdong Provincial Key Laboratory of Animal Molecular Design and Precise Breeding, G. E. T. C. O. G. P. (2023) · Zoological Research · doi:10.24272/j.issn.2095-8137.2023.294 · Cited by 77 · see citing works
Chiang, W., Wei, Y., Kuo, Y.-C., Wei, S., Zhou, A., Zou, Z., Yehl, J., Ranaghan, M. J., Skepner, A. P., Bittker, J. A., et al. (2018) · ACS Chemical Biology · doi:10.1021/acschembio.8b00421 · Cited by 75 · see citing works
Self-citationGalizzi, G., & Carlo, M. D. (2022) · Biology · doi:10.3390/biology11060943 · Cited by 76 · see citing works
Autophagy in Alzheimer's disease and promising modulatory effects of herbal medicine
Zeng, Q., Siu, W. S., Li, L., Yu, J., Liang, S., Cao, M., Ma, M., & Wu, Z. (2019) · Experimental Gerontology · doi:10.1016/j.exger.2019.01.027 · Cited by 64 · see citing works
Comprehensive autophagy evaluation in cardiac disease models
Kaludercic, N., Maiuri, M. C., Kaushik, S., Fernández, Á. F., de Bruijn, J., Castoldi, F., Chen, Y., Ito, J., Mukai, R., Murakawa, T., et al. (2020) · Cardiovascular Research · doi:10.1093/cvr/cvz233 · Cited by 64 · see citing works
Pharmacological modulation of autophagy for Alzheimer's disease therapy: Opportunities and obstacles
Deng, Z., Dong, Y., Zhou, X., Lu, J.-H., & Yue, Z. (2022) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2021.12.009 · Cited by 58 · see citing works
Insulin and Autophagy in Neurodegeneration
de Mello, N. P., Orellana, A. M., Mazucanti, C. H., Lima, G. D. M., Scavone, C., & Kawamoto, E. M. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00491 · Cited by 56 · see citing works
Li, P., Shi, M., Maique, J., Shaffer, J., Yan, S. X., Moe, O. W., & Hu, M. C. (2020) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00504.2019 · Cited by 54 · see citing works
Vitamin K2 Holds Promise for Alzheimer’s Prevention and Treatment
Popescu, A., & German, M. (2021) · Nutrients · doi:10.3390/nu13072206 · Cited by 55 · see citing works
Tang, Z., Cao, J., Yao, J.-L., Fan, X., Zhao, J., Zhao, M., Duan, Q., Han, B., & Duan, S. (2022) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2022.12.099 · Cited by 54 · see citing works
Mechanisms by which autophagy regulates memory capacity in ageing
Risi, M. D., Torromino, G., Tufano, M., Moriceau, S., Pignataro, A., Rivagorda, M., Carrano, N., Middei, S., Settembre, C., Ammassari‐Teule, M., et al. (2020) · Aging Cell · doi:10.1111/acel.13189 · Cited by 53 · see citing works
Yang, J., Zhang, W., Zhang, S., Iyaswamy, A., Sun, J., Wang, J., & Yang, C. (2023) · Aging and Disease · doi:10.14336/ad.2022.0927 · Cited by 48 · see citing works
Self-citationGiovedı̀, S., Ravanelli, M. M., Parisi, B., Bettegazzi, B., & Guarnieri, F. C. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.602116 · Cited by 49 · see citing works
Zhao, Y., Zou, Z., Sun, D., Li, Y., Sinha, S. C., Yu, L., Bennett, L. B., & Levine, B. (2020) · Autophagy · doi:10.1080/15548627.2020.1847798 · Cited by 47 · see citing works
Self-citationThe plasma peptides of Alzheimer’s disease
Florentinus-Mefailoski, A., Bowden, P., Scheltens, P., Killestein, J., Teunissen, C. E., & Marshall, J. G. (2021) · Clinical Proteomics · doi:10.1186/s12014-021-09320-2 · Cited by 46 · see citing works
Compromised autophagy and mitophagy in brain ageing and Alzheimer’s diseases.
Caponio, D., Veverová, K., Zhang, S.-Q., Shi, L., Wong, G., Vyhnalek, M., & Fang, E. F. (2022) · Aging Brain · doi:10.1016/j.nbas.2022.100056 · Cited by 45 · see citing works
Wang, J., Liu, B., Xu, Y. X., Yang, M., Wang, C., Song, M., Liu, J., Wang, W., You, J., Sun, F., et al. (2021) · Aging Cell · doi:10.1111/acel.13333 · Cited by 46 · see citing works
The effects of treadmill exercise on autophagy in hippocampus of APP/PS1 transgenic mice
Zhao, N., Zhang, X., Song, C., Yang, Y., He, B., & Xu, B. (2018) · Neuroreport · doi:10.1097/wnr.0000000000001038 · Cited by 45 · see citing works
Bonam, S. R., Bayry, J., Tschan, M. P., & Muller, S. (2020) · Cells · doi:10.3390/cells9051321 · Cited by 44 · see citing works
Suelves, N., Saleki, S., Ibrahim, T., Palomares, D., Moonen, S., Koper, M. J., Vrancx, C., Vadukul, D. M., Papadopoulos, N., Viceconte, N., et al. (2023) · Acta Neuropathologica Communications · doi:10.1186/s40478-023-01578-x · Cited by 43 · see citing works
Wang, C., Haas, M., Yeo, S. K., Sebti, S., Fernández, Á. F., Zou, Z., Levine, B., & Guan, J. (2021) · Autophagy · doi:10.1080/15548627.2021.1936358 · Cited by 37 · see citing works
Self-citationMolecular Mechanism of Autophagy: Its Role in the Therapy of Alzheimer’s Disease
Zhao, Y., Zhang, Y., Zhang, J., Zhang, X., & Yang, G. (2020) · Current Neuropharmacology · doi:10.2174/1570159x18666200114163636 · Cited by 40 · see citing works
Lin, X., Wen, X., Wei, Z., Guo, K., Shi, F., Huang, T., Wang, W., & Zheng, J. (2021) · Neuroreport · doi:10.1097/wnr.0000000000001599 · Cited by 39 · see citing works
Companys‐Alemany, J., Turcu, A. L., Schneider, M., Müller, C. E., Vázquez, S., Griñán‐Ferré, C., & Pallàs, M. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04438-4 · Cited by 38 · see citing works
Proteolytic cleavage of Beclin 1 exacerbates neurodegeneration
Bieri, G., Lucin, K. M., O’Brien, C. E., Zhang, H., Villeda, S., & Wyss‐Coray, T. (2018) · Molecular Neurodegeneration · doi:10.1186/s13024-018-0302-4 · Cited by 35 · see citing works
Kuramoto, K., Kim, Y.-J., Hong, J. H., & He, C. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109184 · Cited by 40 · see citing works
Self-citationSong, L., Yao, L., Zhang, L., Piao, Z., & Lu, Y. (2020) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-019-01792-2 · Cited by 36 · see citing works
Beclin‐1‐mediated activation of autophagy improves proximal and distal urea cycle disorders
Soria, L. R., Gurung, S., Sabbata, G. D., Perocheau, D. P. B., Angelis, A. D., Bruno, G., Polishchuk, E., Paris, D., Cuomo, P., Motta, A., et al. (2020) · EMBO Molecular Medicine · doi:10.15252/emmm.202013158 · Cited by 33 · see citing works
Protein Kinase C Isozymes and Autophagy during Neurodegenerative Disease Progression
Kaleli, H., Ozer, E., Kaya, V. O., & Kutlu, O. (2020) · Cells · doi:10.3390/cells9030553 · Cited by 30 · see citing works
Xu, J., Kong, L., Oliver, B. A., Li, B., Creasey, E. A., Guzman, G., Schenone, M., Carey, K. L., Carr, S. A., Graham, D. B., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112708 · Cited by 35 · see citing works
Gebril, H. M., Aryasomayajula, A., de Lima, M. R. N., Uhrich, K. E., & Moghe, P. V. (2024) · Translational Neurodegeneration · doi:10.1186/s40035-023-00393-7 · Cited by 36 · see citing works
Carbon monoxide alleviates senescence in diabetic nephropathy by improving autophagy
Chen, L., Mei, G., Jiang, C., Cheng, X., Li, D., Zhao, Y., Chen, H., Wan, C., Yao, P., Gao, C., et al. (2021) · Cell Proliferation · doi:10.1111/cpr.13052 · Cited by 33 · see citing works
Li, S., Poon, C. H., Zhang, Z., Yue, M., Chen, R., Zhang, Y., Hossain, M. F., Pan, Y., Zhao, J. J., Rong, L., et al. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14143 · Cited by 34 · see citing works
Exercise-driven cellular autophagy: A bridge to systematic wellness
Zhou, X.-H., Luo, Y., & Yao, X. (2025) · Journal of Advanced Research · doi:10.1016/j.jare.2024.12.036 · Cited by 33 · see citing works
Griffin, E. F., Yan, X., Caldwell, K. A., & Caldwell, G. A. (2018) · Human Molecular Genetics · doi:10.1093/hmg/ddy308 · Cited by 32 · see citing works
Pharmacological Tools to Modulate Autophagy in Neurodegenerative Diseases
Suresh, S., Chakravorty, A., Giridharan, M., Garimella, L., & Manjithaya, R. R. (2020) · Journal of Molecular Biology · doi:10.1016/j.jmb.2020.02.023 · Cited by 32 · see citing works
Autophagy and Cellular Senescence in Alzheimer's Disease: Key Drivers of Neurodegeneration
Hussain, M. S., Agrawal, N., Ilma, B., Rekha, M. M., Nayak, P. P., Kaur, M., Khachi, A., Goyal, K., Rekha, A., Gupta, S., et al. (2025) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.70503 · Cited by 33 · see citing works
Autophagy in ageing and ageing-related neurodegenerative diseases
Karabiyik, C., Frake, R. A., Park, S. J., Tanasa, M. P., & Rubinsztein, D. C. (2021) · Ageing and Neurodegenerative Diseases · doi:10.20517/and.2021.05 · Cited by 31 · see citing works
Das, S., Murumulla, L., Ghosh, P., & Challa, S. (2025) · BioMetals · doi:10.1007/s10534-025-00665-x · Cited by 31 · see citing works
Autophagy system as a potential therapeutic target for neurodegenerative diseases
Cui, M., Yoshimori, T., & Nakamura, S. (2022) · Neurochemistry International · doi:10.1016/j.neuint.2022.105308 · Cited by 27 · see citing works
Popli, P., Tang, S., Chadchan, S. B., Talwar, C., Rucker, E. B., Guan, X., Monsivais, D., Lydon, J. P., Stallings, C. L., Moley, K. H., et al. (2022) · Developmental Cell · doi:10.1016/j.devcel.2023.03.013 · Cited by 31 · see citing works
Chernyaeva, L., Ratti, G., Teirilä, L., Fudo, S., Rankka, U., Pelkonen, A., Korhonen, P., Leskinen, K., Keskitalo, S., Salokas, K., et al. (2023) · EMBO Reports · doi:10.15252/embr.202256467 · Cited by 26 · see citing works
Fu, Y., Zhang, J., Qin, R., Ren, Y., Zhou, T., Han, B., & Liu, B. (2025) · Pharmacological Reviews · doi:10.1016/j.pharmr.2025.100053 · Cited by 28 · see citing works
Genetically prolonged beige fat in male mice confers long-lasting metabolic health
Wu, R., Park, J., Qian, Y., Shi, Z., Hu, R., Yuan, Y., Xiong, S., Wang, Z., Yan, G., Ong, S., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-38471-z · Cited by 25 · see citing works
Self-citationO’Keefe, L. V., & Denton, D. (2018) · BioMed Research International · doi:10.1155/2018/5195416 · Cited by 24 · see citing works
Hadi, F., Mortaja, M., & Hadi, Z. (2024) · Cell Biochemistry and Function · doi:10.1002/cbf.4085 · Cited by 23 · see citing works
Current Status of Autophagy Enhancers in Metabolic Disorders and Other Diseases
Park, K., & Lee, M. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.811701 · Cited by 24 · see citing works
Chen, M., Wu, Q., Zhu, Z., Huang, A., Zhang, J., Bekhit, A. E. A., Wang, J., & Ding, Y. (2023) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2023.2172547 · Cited by 23 · see citing works
Kamaruzzaman, M. A., Romli, M. H., Abas, R., Vidyadaran, S., Baharuldin, M. T. H., Nasaruddin, M. L., Vishnumukkala, T., Sura, S., Warsito, K., Nor, N. H. M., et al. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1053680 · Cited by 25 · see citing works
Programmable DNA Nanodevices for Applications in Neuroscience
Hivare, P., Panda, C., Gupta, S. K., & Bhatia, D. D. (2021) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.0c00723 · Cited by 21 · see citing works
Loss of ATG7 in microglia impairs UPR, triggers ferroptosis, and weakens amyloid pathology control
Cai, Z., Wang, S., Cao, S. “., Chen, Y., Penati, S., Peng, V., Yuede, C. M., Beatty, W. L., Lin, K., Zhu, Y., et al. (2025) · The Journal of Experimental Medicine · doi:10.1084/jem.20230173 · Cited by 23 · see citing works
Long, T., Chen, X., Zhang, Y., Zhou, Y., He, Y.-N., Zhu, Y., Fu, H., Yu, L., Yu, C., Law, B. Y. K., et al. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115261 · Cited by 21 · see citing works
Genetic enhancement of macroautophagy in vertebrate models of neurodegenerative diseases
Ejlerskov, P., Ashkenazi, A., & Rubinsztein, D. C. (2018) · Neurobiology of Disease · doi:10.1016/j.nbd.2018.04.001 · Cited by 20 · see citing works
The tripartite interaction of phosphate, autophagy, and αKlotho in health maintenance
Shi, M., Maique, J., Shaffer, J., Davidson, T. L., Sebti, S., Fernández, Á. F., Zou, Z., Yan, S. X., Levine, B., Moe, O. W., et al. (2020) · The FASEB Journal · doi:10.1096/fj.201902127r · Cited by 20 · see citing works
Self-citationAutophagy and autophagy‐related molecules in neurodegenerative diseases
Dou, C., Zhang, Y., Zhang, L., & Qin, C. (2022) · Animal Models and Experimental Medicine · doi:10.1002/ame2.12229 · Cited by 19 · see citing works
Dong, X., Liang, Q., Pan, Y.-Z., Wang, X., Kuo, Y.-C., Chiang, W., Zhang, X., Williams, N. S., Rizo, J., Levine, B., et al. (2022) · ACS Medicinal Chemistry Letters · doi:10.1021/acsmedchemlett.2c00309 · Cited by 20 · see citing works
Self-citationModulation of microRNAs through Lifestyle Changes in Alzheimer’s Disease
Pinto-Hernández, P., Castilla-Silgado, J., Coto-Vilcapoma, A., Fernández-Sanjurjo, M., Fernández-García, B., Tomás-Zapico, C., & Iglesias-Gutiérrez, E. (2023) · Nutrients · doi:10.3390/nu15173688 · Cited by 20 · see citing works
Macrophage LRRK2 hyperactivity impairs autophagy and induces Paneth cell dysfunction
Sun, S., Hodel, M., Wang, X., de Vicente, J., Haritunians, T., Debebe, A., Hung, C., Ma, C., Malique, A., Nguyen, H. N., et al. (2024) · Science Immunology · doi:10.1126/sciimmunol.adi7907 · Cited by 20 · see citing works
An autophagy-related protein Becn2 regulates cocaine reward behaviors in the dopaminergic system
Kim, Y.-J., Kong, Q., Yamamoto, S., Kuramoto, K., Huang, M., Wang, N., Hong, J. H., Xiao, T., Levine, B., Qiu, X., et al. (2021) · Science Advances · doi:10.1126/sciadv.abc8310 · Cited by 19 · see citing works
Self-citationcGAS-STING signaling in Alzheimer's disease: Microglial mechanisms and therapeutic opportunities
Fazal, F., Dar, N. J., Ahamad, S., Khan, S., Bano, N., Saha, S., Nazir, A., & Bhat, S. A. (2026) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2025.101444 · Cited by 21 · see citing works
Beclin1 Binds to Enterovirus 71 3D Protein to Promote the Virus Replication
Xiang, Q., Wan, P., Yang, G., Huang, S., Qin, M., Yang, H., Luo, Z., Wu, K., & Wu, J. (2020) · Viruses · doi:10.3390/v12070756 · Cited by 18 · see citing works
Self-citationReduced ULK1 links impaired autophagy and mitophagy to Alzheimer’s disease pathology
Pan, J., Wang, P.-J., Zhang, J., Knapskog, A., Watne, L. O., Wang, H.-L., Lagartos-Donate, M. J., Lautrup, S., Mao, L.-P., Wang, Q., et al. (2026) · Nature Aging · doi:10.1038/s43587-026-01108-z · Cited by 19 · see citing works
Zhang, Z., Chen, S., Jun, S., Xu, X., Hong, Y., Yang, X., Zou, L., Song, Y., Chen, Y., & Tu, J. (2024) · Autophagy · doi:10.1080/15548627.2024.2395727 · Cited by 16 · see citing works
Gressler, A. E., Leng, H.-F., Zinecker, H., & Simon, A. (2023) · Seminars in Immunology · doi:10.1016/j.smim.2023.101838 · Cited by 16 · see citing works
Self-Digestion for Lifespan Extension: Enhanced Autophagy Delays Aging
Arensman, M. D., & Eng, C. H. (2018) · Molecular Cell · doi:10.1016/j.molcel.2018.08.002 · Cited by 16 · see citing works
Sebti, S., Zou, Z., & Shiloh, M. U. (2022) · Autophagy · doi:10.1080/15548627.2022.2111852 · Cited by 14 · see citing works
Structural insights for selective disruption of Beclin 1 binding to Bcl-2
Pan, Y.-Z., Liang, Q., Tomchick, D. R., Brabander, J. K. D., & Rizo, J. (2023) · Communications Biology · doi:10.1038/s42003-023-05467-w · Cited by 14 · see citing works
Sun, F., Wang, J., Meng, L., Zhou, Z., Xu, Y., Yang, M., Li, Y., Jiang, T., Liu, B., & Yan, H. (2024) · British Journal of Pharmacology · doi:10.1111/bph.16400 · Cited by 15 · see citing works
Human autophagy measurement: an underappreciated barrier to translation
Sargeant, T. J., & Bensalem, J. (2021) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2021.09.003 · Cited by 13 · see citing works
Targeting autophagy drug discovery: Targets, indications and development trends
Jiang, M., Wu, W., Xiong, Z., Ye, Z., Ye, Z., & Wu, Z. (2024) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2023.116117 · Cited by 13 · see citing works
Age-related dysfunction of the autophago-lysosomal pathway in human endothelial cells
Mai, S., Brehm, N., Auburger, G. W. J., Bereiter‐Hahn, J., & Jendrach, M. (2019) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-019-02288-x · Cited by 13 · see citing works
Neuroprotective effects of ZL006 in Aβ1–42-treated neuronal cells
Tao, W., Yu, L., Jiang, S., Cao, X., Chen, J., Bao, X.-Y., Li, F., Xu, Y., & Zhu, X.-L. (2020) · Neural Regeneration Research · doi:10.4103/1673-5374.285006 · Cited by 12 · see citing works
Structural insights into Beclin 1 interactions with it's regulators for autophagy modulation
Sarmadhikari, D., & Asthana, S. (2025) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2025.06.044 · Cited by 11 · see citing works
Sadleir, K. R., Popović, J., Khatri, A. W., & Vassar, R. J. (2022) · PLoS ONE · doi:10.1371/journal.pone.0263332 · Cited by 11 · see citing works
Self-citationULK1 confers neuroprotection by regulating microglial/macrophages activation after ischemic stroke
Xiong, Y., Cui, M. Y., Li, Z. L., Fu, Y. Q., Zheng, Y., Yu, Y., Zhang, C., Huang, X. Y., & Chen, B. H. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.111379 · Cited by 10 · see citing works
Pain hypersensitivity is dependent on autophagy protein Beclin 1 in males but not females
Tam, T. H., Zhang, W., Tu, Y., Hicks, J. L., Farcas, S., Kim, D., & Salter, M. W. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114293 · Cited by 10 · see citing works
Self-citation
- Authors
- Rocchi, A., Yamamoto, S., Ting, T., Fan, Y., Sadleir, K., Wang, Y., Zhang, W., Huang, S., Levine, B., Vassar, R., & He, C.
- Affiliations
- Northwestern University (US)
- Howard Hughes Medical Institute (US)
- Corresponding author
- He, Congcong
- ORCID
- Venue
- PLOS Genetics
- Publisher
- Public Library of Science (PLoS)
- Published
- 2017-08-14
- Volume
- 13
- Issue
- 8
- Pages
- e1006962
- ISSN
- 1553-7390 (ISSN-L)
- 1553-7404
- PMC
- PMC5570506
- OpenAlex
- W2749882665
- Cited by
- 166
- References
- 65
- Citations by year
- 2026: 11 · 2025: 24 · 2024: 12 · 2023: 21 · 2022: 24 · 2021: 29 · 2020: 19 · 2019: 10 · 2018: 16
- FWCI
- 9.10
- Type
- journal article
- Language
- en
- Update notices
- new_version (2017-08-24)
- Open access
- gold
- doi.org
- Licence
- Locations
- PLoS Genetics (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by)
- Funders
- Cancer Prevention and Research Institute of Texas (RP120718)
- Northwestern University (AG13854)
- Northeast Normal University
- National Institutes of Health (U19AI199725, 5r01gm078555-08, AG13854, RO1 CA109618)
- University of North Carolina at Chapel Hill
- Fundamental Research Funds for the Central Universities (2412017FZ018)
- National Institute on Aging (AG13854, R01AG030142, R01AG022560, P30AG013854)
- National Cancer Institute (R01CA109618)
- National Institute of General Medical Sciences (R01 GM-078555)
- National Institute of Allergy and Infectious Diseases (U19AI109725, T32AI007163)
- Topics
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- Alzheimer's disease, autophagy, Beclin-1, Bcl-2, amyloid-beta oligomers, autophagosomes, cognitive decline, voluntary exercise, autophagy inducers, genetic mouse models
- MeSH terms
- Beclin-1, Alzheimer Disease, Animals, Autophagy, Cognition, Disease Models, Animal, HeLa Cells, Humans, Male, Memory, Mice, Inbred C57BL, Neurons, Amyloid beta-Peptides, Point Mutation, Sequence Analysis, DNA, Proto-Oncogene Proteins c-bcl-2, In Situ Nick-End Labeling, Mice, Gene Knock-In Techniques, HEK293 Cells
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