Nature reviews. Neuroscience, Journal Year: 2018, Volume and Issue: 19(10), P. 622 - 635
Published: Sept. 11, 2018
Language: Английский
Nature reviews. Neuroscience, Journal Year: 2018, Volume and Issue: 19(10), P. 622 - 635
Published: Sept. 11, 2018
Language: Английский
Molecular Neurodegeneration, Journal Year: 2019, Volume and Issue: 14(1)
Published: Aug. 2, 2019
Alzheimer's disease is a progressive neurodegenerative most often associated with memory deficits and cognitive decline, although less common clinical presentations are increasingly recognized. The cardinal pathological features of the have been known for more than one hundred years, today presence these amyloid plaques neurofibrillary tangles still required diagnosis. cause dementia globally. There remain no effective treatment options great majority patients, primary causes unknown except in small number familial cases driven by genetic mutations. Confounding efforts to develop diagnostic tools disease-modifying therapies realization that mixed proteinopathy (amyloid tau) frequently other age-related processes such as cerebrovascular Lewy body disease. Defining relationships between interdependence various co-pathologies remains an active area investigation. This review outlines etiologically-linked pathologic disease, well those inevitable findings uncertain significance, granulovacuolar degeneration Hirano bodies. Other frequent, but not inevitable, also discussed, including can clinically mimic These include TDP-43 proteinopathies argyrophilic grain purpose this provide overview pathology, its defining substrates related pathologies affect diagnosis treatment.
Language: Английский
Citations
2414Cell, Journal Year: 2019, Volume and Issue: 179(2), P. 312 - 339
Published: Sept. 26, 2019
Language: Английский
Citations
2363Nature Reviews Neurology, Journal Year: 2020, Volume and Issue: 17(3), P. 157 - 172
Published: Dec. 14, 2020
Language: Английский
Citations
2100New England Journal of Medicine, Journal Year: 2018, Volume and Issue: 378(2), P. 169 - 180
Published: Jan. 10, 2018
Multiple sclerosis affects more than 2 million people worldwide and is currently incurable. A number of interventions to modify the course multiple have been developed that offer new insight into disease mechanisms.
Language: Английский
Citations
1963Immunity, Journal Year: 2017, Volume and Issue: 46(6), P. 957 - 967
Published: June 1, 2017
Language: Английский
Citations
1912Immunity, Journal Year: 2018, Volume and Issue: 50(1), P. 253 - 271.e6
Published: Nov. 21, 2018
Language: Английский
Citations
1747Nature Neuroscience, Journal Year: 2021, Volume and Issue: 24(3), P. 312 - 325
Published: Feb. 15, 2021
Language: Английский
Citations
1683Translational Neurodegeneration, Journal Year: 2020, Volume and Issue: 9(1)
Published: Nov. 26, 2020
Abstract Neuroinflammation is associated with neurodegenerative diseases, such as Alzheimer’s disease, Parkinson’s and amyotrophic lateral sclerosis. Microglia astrocytes are key regulators of inflammatory responses in the central nervous system. The activation microglia heterogeneous traditionally categorized neurotoxic (M1-phenotype A1-phenotype astrocytes) or neuroprotective (M2-phenotype A2-phenotype astrocytes). However, this dichotomized classification may not reflect various phenotypes astrocytes. relationship between these activated glial cells also very complicated, phenotypic distribution can change, based on progression diseases. A better understanding roles diseases essential for developing effective therapies. In review, we discuss response focusing contributions their relationship. addition, biomarkers to measure neuroinflammation studies therapeutic drugs that modulate neuroinflammation.
Language: Английский
Citations
1675Nature reviews. Immunology, Journal Year: 2017, Volume and Issue: 18(4), P. 225 - 242
Published: Nov. 20, 2017
Language: Английский
Citations
1633The Journal of Cell Biology, Journal Year: 2017, Volume and Issue: 217(2), P. 459 - 472
Published: Dec. 1, 2017
Proliferation and activation of microglia in the brain, concentrated around amyloid plaques, is a prominent feature Alzheimer’s disease (AD). Human genetics data point to key role for pathogenesis AD. The majority risk genes AD are highly expressed (and many selectively expressed) by brain. There mounting evidence that protect against incidence AD, as impaired microglial activities altered responses β-amyloid associated with increased risk. On other hand, there also abundant activated can be harmful neurons. Microglia mediate synapse loss engulfment synapses, likely via complement-dependent mechanism; they exacerbate tau pathology secrete inflammatory factors injure neurons directly or neurotoxic astrocytes. Gene expression profiles indicate multiple states neurodegenerative settings, which might explain disparate roles development progression pathology.
Language: Английский
Citations
1584