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Intracellular Clusterin Interacts with Brain Isoforms of the Bridging Integrator 1 and with the Microtubule-Associated Protein Tau in Alzheimer's Disease
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BIN1 isoforms 9 and 10 are ubiquitously expressed and are also detected in the brain.
“Isoforms 9 and 10 are ubiquitously expressed and are also detected in the brain [11].”
From BIN1 protein isoforms are differentially expressed in astrocytes, neurons, and microglia: neuronal and astrocyte BIN1 are implicated in tau pathology (2020) · cites this paper as [11]
BIN1 has 10 isoforms expressed in the central nervous system.
“BIN1 has 10 isoforms that are expressed in the Central Nervous System (CNS).”
From BIN1 protein isoforms are differentially expressed in astrocytes, neurons, and microglia: neuronal and astrocyte BIN1 are implicated in tau pathology (2020) · cites this paper as [11]
BIN1 isoforms are translated into proteins differently in neurons and astrocytes: cultured neurons mostly express isoforms 1, 3, 5 and 7 while cultured astrocytes express isoforms 2, 5, 9 and 10.
“It was reported that BIN1 isoforms are translated into proteins differently in neurons and astrocytes: cultured neurons mostly express isoforms 1, 3, 5 and 7 while cultured astrocytes express isoforms 2, 5, 9 and 10 [11].”
From BIN1 protein isoforms are differentially expressed in astrocytes, neurons, and microglia: neuronal and astrocyte BIN1 are implicated in tau pathology (2020) · cites this paper as [11]
Isoform 1 and 3 are expressed in neurons and isoform 2 in astrocytes.
“are consistent with previously published reports of isoform 1 and 3 expression in neurons and isoform 2 in astrocytes [11].”
From BIN1 protein isoforms are differentially expressed in astrocytes, neurons, and microglia: neuronal and astrocyte BIN1 are implicated in tau pathology (2020) · cites this paper as [11]
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Harold, D., Abraham, R., Hollingworth, P., Sims, R., Gerrish, A., Hamshere, M. L., Pahwa, J. S., Moskvina, V., Dowzell, K., Williams, A., et al. (2009) · Nature Genetics · doi:10.1038/ng.440 · Cited by 3,326
Naj, A. C., Jun, G., Beecham, G. W., Wang, L.-S., Vardarajan, B. N., Buros, J., Gallins, P. J., Buxbaum, J. D., Jarvik, G. P., Crane, P. K., et al. (2011) · Nature Genetics · doi:10.1038/ng.801 · Cited by 1,901
Human ApoE isoforms differentially regulate brain amyloid-β peptide clearance
Castellano, J. M., Kim, J., Stewart, F. R., Jiang, H., DeMattos, R. B., Patterson, B. W., Fagan, A. M., Morris, J. C., Mawuenyega, K. G., Cruchaga, C., et al. (2011) · Science Translational Medicine · doi:10.1126/scitranslmed.3002156 · Cited by 1,242 · cited 2×
“Because of previously reported effects of apoE genotype on brain amyloid burden [24], we also characterized subjects for their APOE variants.”
BackgroundClusterin inhibits apoptosis by interacting with activated Bax
Zhang, H., Kim, J. K., Edwards, C. A., Xu, Z., Taichman, R., & Wang, C.-Y. (2005) · Nature Cell Biology · doi:10.1038/ncb1291 · Cited by 453
Apolipoprotein J: structure and tissue distribution
De Silva, H. V., Harmony, J. A. K., Stuart, W. D., Gil, C. M., & Robbins, J. (1990) · Biochemistry · doi:10.1021/bi00474a025 · Cited by 353
May, P. C., Lampert-Etchells, M., Johnson, S. A., Poirier, J., Masters, J. N., & Finch, C. E. (1990) · Neuron · doi:10.1016/0896-6273(90)90342-d · Cited by 339
Expression of Novel Alzheimer’s Disease Risk Genes in Control and Alzheimer’s Disease Brains
Karch, C. M., Jeng, A. T., Nowotny, P., Cady, J., Cruchaga, C., & Goate, A. M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0050976 · Cited by 328
Corneveaux, J. J., Myers, A. J., Allen, A. N., Pruzin, J. J., Ramirez, M., Engel, A., Nalls, M. A., Chen, K., Lee, W., Chewning, K., et al. (2010) · Human Molecular Genetics · doi:10.1093/hmg/ddq221 · Cited by 237
Distribution of clusterin in Alzheimer brain tissue
McGeer, P. L., Kawamata, T., & Walker, D. G. (1992) · Brain Research · doi:10.1016/0006-8993(92)90071-g · Cited by 212 · cited 1×
“Induction of CLU mRNA is observed within pyramidal neurons of the hippocampus and the entorhinal cortex of AD patients [20,21], and CLU immunoreactivity is found in association with neutrophil threads, neurofibrillary tangles and amyloid plaques [20].”
BackgroundReplication of CLU, CR1, and PICALM Associations With Alzheimer Disease
Carrasquillo, M. M., Belbin, O., Hunter, T. A., Ma, L., Bisceglio, G. D., Zou, F., Crook, J. E., Pankratz, V. S., Dickson, D. W., Graff-Radford, N. R., et al. (2010) · Archives of Neurology · doi:10.1001/archneurol.2010.147 · Cited by 208
Shulman, J. M., Imboywa, S., Giagtzoglou, N., Powers, M. P., Hu, Y., Devenport, D., Chipendo, P., Chibnik, L. B., Diamond, A., Perrimon, N., et al. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddt478 · Cited by 167
Functional and structural properties of lipid-associated apolipoprotein J (clusterin)
CALERO, M., TOKUDA, T., ROSTAGNO, A., KUMAR, A., ZLOKOVIC, B., FRANGIONE, B., & GHISO, J. (1999) · Biochemical Journal · doi:10.1042/bj3440375 · Cited by 98
Flagged first, then by citations
Research works printed but not linked: 45
- JC Lambert, 2009, Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease, Nat Genet, 41, 1094, 10.1038/ng.439 · DOI · Paper page
- G Jun, 2010, Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes, Arch Neurol, 67, 1473, 10.1001/archneurol.2010.201 · DOI · Paper page
- JH Lee, 2011, Identification of novel loci for Alzheimer disease and replication of CLU, PICALM, and BIN1 in Caribbean Hispanic individuals, Arch Neurol, 68, 320
- EM Wijsman, 2011, Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE, PLoS Genet, 7, e1001308, 10.1371/journal.pgen.1001308 · DOI
- K Bettens, 2012, Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer risk, Mol Neurodegener, 7, 3, 10.1186/1750-1326-7-3 · DOI
- T Nuutinen, 2009, Clusterin: a forgotten player in Alzheimer's disease, Brain Res Rev, 61, 89, 10.1016/j.brainresrev.2009.05.007 · DOI · Paper page
- P Nizard, 2007, Stress-induced retrotranslocation of clusterin/ApoJ into the cytosol, Traffic, 8, 554, 10.1111/j.1600-0854.2007.00549.x · DOI
- S Bettuzzi, 2009, Nuclear CLU (nCLU) and the fate of the cell, Adv Cancer Res, 104, 59, 10.1016/S0065-230X(09)04005-6 · DOI
- H Prochnow, 2013, Non-secreted clusterin isoforms are translated in rare amounts from distinct human mRNA variants and do not affect Bax-mediated apoptosis or the NF-κB signaling pathway, PLoS One, 8, e75303, 10.1371/journal.pone.0075303 · DOI
- N Kim, 2011, Human nuclear clusterin mediates apoptosis by interacting with Bcl-XL through C-terminal coiled coil domain, J Cell Physiol, 227, 1157, 10.1002/jcp.22836 · DOI
- R Killick, 2014, Clusterin regulates β-amyloid toxicity via Dickkopf-1-driven induction of the wnt-PCP-JNK pathway, Mol Psychiatry, 19, 88, 10.1038/mp.2012.163 · DOI · Paper page
- JR Duguid, 1989, Changes in brain gene expression shared by scrapie and Alzheimer disease, Proc Natl Acad Sci USA, 86, 7260, 10.1073/pnas.86.18.7260 · DOI
- AM Lidström, 1998, Clusterin (apolipoprotein J) protein levels are increased in hippocampus and in frontal cortex in Alzheimer's disease, Exp Neurol, 154, 511, 10.1006/exnr.1998.6892 · DOI
- RB DeMattos, 2002, Clusterin promotes amyloid plaque formation and is critical for neuritic toxicity in a mouse model of Alzheimer's disease, Proc Natl Acad Sci USA, 99, 10843, 10.1073/pnas.162228299 · DOI · Paper page
- RB DeMattos, 2004, ApoE and clusterin cooperatively suppress Abeta levels and deposition: evidence that ApoE regulates extracellular Abeta metabolism in vivo, Neuron, 41, 193, 10.1016/S0896-6273(03)00850-X · DOI · Paper page
- P Narayan, 2012, Amyloid-β oligomers are sequestered by both intracellular and extracellular chaperones, Biochemistry, 51, 9270, 10.1021/bi301277k · DOI
- R Cascella, 2013, Extracellular chaperones prevent Aβ42-induced toxicity in rat brains, Biochim Biophys Acta, 1832, 1217, 10.1016/j.bbadis.2013.04.012 · DOI
- S Baig, 2012, Clusterin mRNA and protein in Alzheimer's disease, J Alzheimers Dis, 28, 337, 10.3233/JAD-2011-110473 · DOI
- TM Hughes, 2014, Markers of cholesterol transport are associated with amyloid deposition in the brain, Neurobiol Aging, 35, 802, 10.1016/j.neurobiolaging.2013.09.040 · DOI
- MN Braskie, 2011, Common Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adults, J Neurosci, 31, 6764, 10.1523/JNEUROSCI.5794-10.2011 · DOI
- S Erk, 2011, Hippocampal function in healthy carriers of the CLU Alzheimer's disease risk variant, J Neurosci, 31, 18180, 10.1523/JNEUROSCI.4960-11.2011 · DOI
- M Thambisetty, 2013, Alzheimer risk variant CLU and brain function during aging, Biol Psychiatry, 73, 399, 10.1016/j.biopsych.2012.05.026 · DOI
- D Sakamuro, 1996, BIN1 is a novel MYC-interacting protein with features of a tumour suppressor, Nat Genet, 14, 69, 10.1038/ng0996-69 · DOI · Paper page
- S Seshadri, 2010, Genome-wide analysis of genetic loci associated with Alzheimer disease, JAMA, 303, 1832, 10.1001/jama.2010.574 · DOI · Paper page
- MM Carrasquillo, 2011, Replication of BIN1 association with Alzheimer's disease and evaluation of genetic interactions, J Alzheimers Dis, 24, 751, 10.3233/JAD-2011-101932 · DOI
- X Hu, 2011, Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease, PLoS One, 6, e16616, 10.1371/journal.pone.0016616 · DOI
- MW Logue, 2011, A comprehensive genetic association study of Alzheimer disease in African Americans, Arch Neurol, 68, 1569, 10.1001/archneurol.2011.646 · DOI
- MS Tan, 2013, Bridging integrator 1 (BIN1): form, function, and Alzheimer's disease, Trends Mol Med, 19, 594, 10.1016/j.molmed.2013.06.004 · DOI
- J Chapuis, 2013, Increased expression of BIN1 mediates Alzheimer genetic risk by modulating Tau pathology, Mol Psychiatry, 18, 1225, 10.1038/mp.2013.1 · DOI · Paper page
- C Cruchaga, 2014, Genetic discoveries in AD using CSF amyloid and tau, Curr Genet Med Rep, 2, 23, 10.1007/s40142-014-0031-0 · DOI
- AM Fagan, 2011, Comparison of analytical platforms for cerebrospinal fluid measures of β-amyloid 1–42, total tau, and p-tau181 for identifying Alzheimer disease amyloid plaque pathology, Arch Neurol, 68, 1137, 10.1001/archneurol.2011.105 · DOI
- NS Schoonenboom, 2012, Cerebrospinal fluid markers for differential dementia diagnosis in a large memory clinic cohort, Neurology, 78, 47, 10.1212/WNL.0b013e31823ed0f0 · DOI · Paper page
- BM Schjeide, 2011, The role of clusterin, complement receptor 1, and phosphatidylinositol binding clathrin assembly protein in Alzheimer disease risk and cerebrospinal fluid biomarker levels, Arch Gen Psychiatry, 68, 207, 10.1001/archgenpsychiatry.2010.196 · DOI
- LS Elias-Sonnenschein, 2012, Relationship between genetic risk factors and markers for Alzheimer's disease pathology, Biomark Med, 6, 477, 10.2217/bmm.12.56 · DOI
- AM Nilselid, 2006, Clusterin in cerebrospinal fluid: analysis of carbohydrates and quantification of native and glycosylated forms, Neurochem Int, 48, 718, 10.1016/j.neuint.2005.12.005 · DOI · Paper page
- C Sihlbom, 2008, Structural and quantitative comparison of cerebrospinal fluid glycoproteins in Alzheimer's disease patients and healthy individuals, Neurochem Res, 33, 1332, 10.1007/s11064-008-9588-x · DOI
- M Ramsden, 2005, Age-dependent neurofibrillary tangle formation, neuron loss, and memory impairment in a mouse model of human tauopathy (P301L), J Neurosci, 25, 10637, 10.1523/JNEUROSCI.3279-05.2005 · DOI · Paper page
- CR Yang, 2000, Nuclear clusterin/XIP8, an x-ray-induced Ku70-binding protein that signals cell death, Proc Natl Acad Sci USA, 97, 5907, 10.1073/pnas.97.11.5907 · DOI
- SW Kang, 2005, Clusterin interacts with SCLIP (SCG10-like protein) and promotes neurite outgrowth of PC12 cells, Exp Cell Res, 309, 305, 10.1016/j.yexcr.2005.06.012 · DOI
- EM Schrijvers, 2011, Plasma clusterin and the risk of Alzheimer disease, JAMA, 305, 1322, 10.1001/jama.2011.381 · DOI · Paper page
- RS Desikan, 2014, The Role of Clusterin in Amyloid-β-Associated Neurodegeneration, JAMA Neurol, 71, 180, 10.1001/jamaneurol.2013.4560 · DOI · Paper page
- SW Kang, 2013, Unglycosylated clusterin variant accumulates in the endoplasmic reticulum and induces cytotoxicity, Int J Biochem Cell Biol, 45, 221, 10.1016/j.biocel.2012.11.014 · DOI
- S Barghorn, 2000, Structure, microtubule interactions, and paired helical filament aggregation by tau mutants of frontotemporal dementias, Biochemistry, 39, 11714, 10.1021/bi000850r · DOI
- JD Ellis, 2012, Tissue-specific alternative splicing remodels protein-protein interaction networks, Mol Cell, 46, 884, 10.1016/j.molcel.2012.05.037 · DOI · Paper page
- K Ando, 2013, Clathrin adaptor CALM/PICALM is associated with neurofibrillary tangles and is cleaved in Alzheimer's brains, Acta Neuropathol, 125, 861, 10.1007/s00401-013-1111-z · DOI · Paper page
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Metadata
- Authors
- Zhou, Y., Hayashi, I., Wong, J., Tugusheva, K., Renger, J. J., & Zerbinatti, C.
- Venue
- PLoS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2014-07-22
- Volume
- 9
- Issue
- 7
- Pages
- e103187
- ISSN
- 1932-6203
- PMC
- PMC4106906
- Cited by
- 72
- References
- 12
- Language
- en
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