Suárez-Calvet, Marc
Kleinberger, Gernot
Araque Caballero, Miguel Ángel
Brendel, Matthias
Rominger, Axel
Alcolea, Daniel
Fortea, Juan
Lleó, Alberto
Blesa, Rafael
Gispert, Juan Domingo
Sanchez-Valle, Raquel
Antonell, Anna
Rami Gonzalez, Lorena
Molinuevo, José Luis
Brosseron, Frederic
Traschütz, Andreas
Heneka, Michael
Struyfs, Hanne
Engelborghs, Sebastiaan
Sleegers, Kristel
Van Broeckhoven, Christine
Zetterberg, Henrik
Nellgård, Bengt
Blennow, Kaj
Crispin, Alexander
Ewers, Michael
Haass, Christian
Universitat Autònoma de Barcelona
2016
2 is an innate immune receptor expressed on the surface of microglia. Loss-of-function mutations of 2 are associated with increased risk of Alzheimer's disease (). 2 is a type-1 protein with an ectodomain that is proteolytically cleaved and released into the extracellular space as a soluble variant (2), which can be measured in the cerebrospinal fluid (). In this cross-sectional multicenter study, we investigated whether levels of 2 are changed during the clinical course of , and in cognitively normal individuals with suspected non- pathology (). 2 levels were higher in mild cognitive impairment due to than in all other groups and controls. individuals also had significantly increased 2 compared to controls. Moreover, increased 2 levels were associated with higher total tau and phospho-tau, which are markers of neuronal degeneration and tau pathology. Our data demonstrate that 2 levels are increased in the early symptomatic phase of , probably reflecting a corresponding change of the microglia activation status in response to neuronal degeneration.
English
Alzheimer's disease; Biomarkers; Microglia; Neurodegeneration; TREM2; Biomarkers & Diagnostic Imaging; Neuroscience
European Commission P7-2007-2013
EMBO Molecular Medicine ; Vol. 8 (march 2016), p. 466-476
open access
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