タウオパチー
タウオパチー
(tauopathy から転送)
出典: フリー百科事典『ウィキペディア(Wikipedia)』 (2020/04/25 09:03 UTC 版)
タウオパチー(英: tauopathy)は、ヒトの脳の神経細胞やグリア細胞において、タウタンパク質による神経原線維変化(neurofibrillary tangle、NFT)やglial fibrillary tangleの形成を伴う神経変性疾患群である。タウと呼ばれる微小管結合タンパク質の過剰なリン酸化によって生じ、その結果タウは微小管から解離し不溶性の凝集体を形成する[1]。こうした凝集体は対らせん状細線維(paired helical filament)とも呼ばれる。凝集の形成過程はあまり解明されておらず、それらがアルツハイマー病の主要因であるのか、それとも補助的役割を果たしているだけであるのかについても明らかではない。
- ^ a b “Propagation of Tau aggregates”. Molecular Brain 10 (1): 18. (May 2017). doi:10.1186/s13041-017-0298-7. PMC: 5450399. PMID 28558799 .
- ^ Alzheimer 'tau' protein far surpasses amyloid in predicting toll on brain tissue
- ^ a b c “Neuropathology of non-Alzheimer degenerative disorders”. International Journal of Clinical and Experimental Pathology 3 (1): 1–23. (August 2009). PMC: 2776269. PMID 19918325 .
- ^ “Abnormal hyperphosphorylation of tau: sites, regulation, and molecular mechanism of neurofibrillary degeneration”. Journal of Alzheimer's Disease 33 Suppl 1: S123-39. (2013). doi:10.3233/JAD-2012-129031. PMID 22710920.
- ^ “Tau in physiology and pathology”. Nature Reviews. Neuroscience 17 (1): 5–21. (January 2016). doi:10.1038/nrn.2015.1. PMID 26631930.
- ^ “Neuropathological stageing of Alzheimer-related changes”. Acta Neuropathologica 82 (4): 239–59. (1991). doi:10.1007/BF00308809. PMID 1759558.
- ^ “The MAPT H1 haplotype is associated with tangle-predominant dementia”. Acta Neuropathologica 124 (5): 693–704. (November 2012). doi:10.1007/s00401-012-1017-1. PMC: 3608475. PMID 22802095 .
- ^ “Neurofibrillary tangle-predominant dementia: comparison with classical Alzheimer disease”. Acta Neuropathologica 113 (2): 107–17. (February 2007). doi:10.1007/s00401-006-0156-7. PMID 17089134.
- ^ “The first NINDS/NIBIB consensus meeting to define neuropathological criteria for the diagnosis of chronic traumatic encephalopathy”. Acta Neuropathologica 131 (1): 75–86. (January 2016). doi:10.1007/s00401-015-1515-z. PMC: 4698281. PMID 26667418 .
- ^ “Immunocytochemistry of neurofibrillary tangles in dementia pugilistica and Alzheimer's disease: evidence for common genesis”. Lancet 2 (8626–8627): 1456–8. (1988). doi:10.1016/S0140-6736(88)90934-8. PMID 2904573.
- ^ “Progressive supranuclear palsy: clinicopathological concepts and diagnostic challenges”. The Lancet. Neurology 8 (3): 270–9. (March 2009). doi:10.1016/S1474-4422(09)70042-0. PMID 19233037.
- ^ “Deciphering the genetic basis of Alzheimer's disease”. Annual Review of Genomics and Human Genetics 3: 67–99. (2002). doi:10.1146/annurev.genom.3.022502.103022. PMID 12142353.
- ^ “Amyotrophic lateral sclerosis/parkinsonism-dementia complex of Guam: quantitative neuropathology, immunohistochemical analysis of neuronal vulnerability, and comparison with related neurodegenerative disorders”. Acta Neuropathologica 88 (5): 397–404. (1994). doi:10.1007/BF00389490. PMID 7847067.
- ^ “Tau-associated neuropathology in ganglion cell tumours increases with patient age but appears unrelated to ApoE genotype”. Neuropathology and Applied Neurobiology 27 (3): 197–205. (June 2001). doi:10.1046/j.1365-2990.2001.00311.x. PMID 11489139.
- ^ “Meningio-angiomatosis: a report of six cases with special reference to the occurrence of neurofibrillary tangles”. Journal of Neuropathology and Experimental Neurology 45 (4): 426–46. (July 1986). doi:10.1097/00005072-198607000-00005. PMID 3088216.
- ^ “Neurofibrillary changes in the cerebral cortex of a patient with subacute sclerosing panencephalitis (SSPE)”. Acta Neuropathologica 48 (2): 157–60. (November 1979). doi:10.1007/BF00691159. PMID 506699.
- ^ “Alzheimer neurofibrillary tangles in diseases other than senile and presenile dementia”. Annals of Neurology 5 (3): 288–94. (March 1979). doi:10.1002/ana.410050311. PMID 156000.
- ^ Wang, Lu-Ning; Zhu, Ming-Wei; Feng, Ya-Qing; Wang, Jian-Hua (2006-06). “Pick's disease with Pick bodies combined with progressive supranuclear palsy without tuft-shaped astrocytes: a clinical, neuroradiologic and pathological study of an autopsied case”. Neuropathology: Official Journal of the Japanese Society of Neuropathology 26 (3): 222–230. doi:10.1111/j.1440-1789.2006.00671.x. ISSN 0919-6544. PMID 16771179 .
- ^ “Argyrophilic grain disease”. Brain 131 (Pt 6): 1416–32. (June 2008). doi:10.1093/brain/awm305. PMID 18234698.
- ^ “Argyrophilic grains: a distinct disease or an additive pathology?”. Neurobiology of Aging 29 (4): 566–73. (April 2008). doi:10.1016/j.neurobiolaging.2006.10.032. PMC: 2727715. PMID 17188783 .
- ^ “[Argyrophilic grain disease: synergistic component of dementia?]” (French). Revue Neurologique 166 (4): 428–32. (April 2010). doi:10.1016/j.neurol.2009.10.012. PMID 19963233.
- ^ a b “[Argyrophilic grain disease: differentiation from Alzheimer disease]”. Der Pathologe 20 (3): 159–68. (May 1999). doi:10.1007/s002920050339. PMID 10412175.
- ^ “Dementia with grains (argyrophilic grain disease)”. Brain Pathology 8 (2): 377–86. (April 1998). doi:10.1111/j.1750-3639.1998.tb00161.x. PMID 9546294.
- ^ “Alpha-synuclein and tau: teammates in neurodegeneration?”. Molecular Neurodegeneration 9: 43. (October 2014). doi:10.1186/1750-1326-9-43. PMC: 4230508. PMID 25352339 .
- ^ “Extrapyramidal syndromes in frontotemporal degeneration”. Journal of Molecular Neuroscience 45 (3): 336–42. (November 2011). doi:10.1007/s12031-011-9616-1. PMID 21887521.
- 1 タウオパチーとは
- 2 タウオパチーの概要
- 3 関連項目
- tauopathyのページへのリンク