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   <dc:title>Inflammatory Response in the Hippocampus of PS1M146L/APP751SL Mouse Model of Alzheimer’s Disease: Age-Dependent Switch in the Microglial Phenotype from Alternative to Classic.</dc:title>
   <dc:creator>Jiménez, Sebastián</dc:creator>
   <dc:creator>Baglietto-Vargas, David</dc:creator>
   <dc:creator>Caballero, Cristina</dc:creator>
   <dc:creator>Moreno-González, Inés</dc:creator>
   <dc:creator>Torres, Manuel</dc:creator>
   <dc:creator>Sánchez-Varo, Raquel María</dc:creator>
   <dc:creator>Ruano, Diego</dc:creator>
   <dc:creator>Vizuete, Marisa</dc:creator>
   <dc:creator>Gutiérrez-Pérez, Antonia</dc:creator>
   <dc:creator>Vitorica Ferrández, Javier</dc:creator>
   <dc:creator>Baglietto-Vargas, David</dc:creator>
   <dc:subject>Alzheimer, Enfermedad de - Modelos animales</dc:subject>
   <dc:subject>Microglia</dc:subject>
   <dc:subject>Hipocampo (Cerebro)</dc:subject>
   <dcterms:abstract>Although the microglial activation is concomitant to the Alzheimer's disease, its precise role (neuroprotection vs neurodegeneration) has not yet been resolved. Here, we show the existence of an age-dependent phenotypic change of microglial activation in the hippocampus of PS1xAPP model, from an alternative activation state with Aβ phagocytic capabilities (at 6 months) to a classic cytotoxic phenotype (expressing TNF-α and related factors) at 18 months of age. This switch was coincident with high levels of soluble Aβ oligomers and a significant pyramidal neurodegeneration. In vitro assays, using astromicroglial cultures, demonstrated that oligomeric Aβ42 and soluble extracts from 18-month-old PS1xAPP hippocampus produced a potent TNF-α induction whereas monomeric Aβ42 and soluble extract from 6- or 18-month-old control and 6-month-old PS1xAPP hippocampi produced no stimulation. This stimulatory effect was avoided by immunodepletion using 6E10 or A11. In conclusion, our results show evidence of a switch in the activated microglia phenotype from alternative, at the beginning of Aβ pathology, to a classical at advanced stage of the disease in this model. This change was induced, at least in part, by the age-dependent accumulation of extracellular soluble Aβ oligomers. Finally, these cytotoxic activated microglial cells could participate in the neuronal lost observed in AD.</dcterms:abstract>
   <dcterms:dateAccepted>2024-07-03T08:28:04Z</dcterms:dateAccepted>
   <dcterms:available>2024-07-03T08:28:04Z</dcterms:available>
   <dcterms:created>2024-07-03T08:28:04Z</dcterms:created>
   <dcterms:issued>2008</dcterms:issued>
   <dc:type>journal article</dc:type>
   <dc:identifier>Jimenez S, Baglietto-Vargas D, Caballero C, Moreno-Gonzalez I, Torres M, Sanchez-Varo R, Ruano D, Vizuete M, Gutierrez A, Vitorica J. Inflammatory response in the hippocampus of PS1M146L/APP751SL mouse model of Alzheimer's disease: age-dependent switch in the microglial phenotype from alternative to classic. J Neurosci. 2008 Nov 5;28(45):11650-61. doi: 10.1523/JNEUROSCI.3024-08.2008. PMID: 18987201; PMCID: PMC6671312.</dc:identifier>
   <dc:identifier>https://hdl.handle.net/10630/31853</dc:identifier>
   <dc:identifier>10.1523/JNEUROSCI.3024-08.2008</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
   <dc:rights>open access</dc:rights>
   <dc:rights>Atribución 4.0 Internacional</dc:rights>
   <dc:publisher>Society for Neuroscience</dc:publisher>
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