<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-28T22:55:41Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/40712" metadataPrefix="qdc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/40712</identifier><datestamp>2026-02-03T11:29:22Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37953</setSpec></header><metadata><qdc:qualifieddc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Inflammatory microglia are glycolytic and iron retentive and typify the microglia in APP/PS1 mice.</dc:title>
   <dc:creator>Holland, Roland</dc:creator>
   <dc:creator>McIntosh, Allison</dc:creator>
   <dc:creator>Finucane, Orla</dc:creator>
   <dc:creator>Mela-Rivas, Virginia</dc:creator>
   <dc:creator>Rubio-Araiz, Ana</dc:creator>
   <dc:creator>Timmons, G.</dc:creator>
   <dc:creator>McCarthy, S.</dc:creator>
   <dc:creator>Gunko, Y.K.</dc:creator>
   <dc:creator>Lynch, Marina Ann</dc:creator>
   <dc:subject>Microglia</dc:subject>
   <dc:subject>Glucólisis</dc:subject>
   <dc:subject>Hierro - Metabolismo</dc:subject>
   <dc:subject>Inflamación (Patología)</dc:subject>
   <dc:subject>Modelos animales en investigación</dc:subject>
   <dcterms:abstract>Microglia, like macrophages, can adopt inflammatory and anti-inflammatory phenotypes&#xd;
depending on the stimulus. At the polar ends of the spectrum of phenotypes are the socalled M1-like inflammatory cells and M2-like anti-inflammatory cells that are stimulated&#xd;
in vitro by lipopolysaccharide (LPS) or interferon- (IFN) and interleukin-4 (IL-4)&#xd;
respectively. In macrophages, the evidence indicates that these phenotypes have different&#xd;
metabolic profiles with M1-like cells switching to glycolysis as their main source of ATP&#xd;
and M2-like cells utilizing oxidative phosphorylation. There is a paucity of information&#xd;
regarding the metabolic signatures in inflammatory and anti-inflammatory microglial&#xd;
phenotypes. Here, we polarized primary microglia with IFN and show that the&#xd;
characteristic increases in nitric oxide synthase 2 (NOS2) and tumor necrosis factor-α&#xd;
(TNF) were accompanied by increased glycolysis and an increase in the expression of 6-&#xd;
phosphofructo-2-kinase/fructose-2,6-biphosphatase (PFKFB)3, an enzyme that plays a&#xd;
significant role in driving glycolysis. These changes were associated with increased&#xd;
expression of ferritin and retention of iron in microglia. In contrast with the IFN-induced&#xd;
changes IL-4, which predictably increased mRNA expression of mannose receptor C, type&#xd;
1 (MRC-1) and arginase 1 (Arg1), also increased oxygen consumption in microglia. The&#xd;
data indicate distinct metabolic signatures of inflammatory and anti-inflammatory&#xd;
microglia that are also distinguishable by their iron handling profiles.</dcterms:abstract>
   <dcterms:dateAccepted>2025-11-13T07:52:49Z</dcterms:dateAccepted>
   <dcterms:available>2025-11-13T07:52:49Z</dcterms:available>
   <dcterms:created>2025-11-13T07:52:49Z</dcterms:created>
   <dcterms:issued>2018-02</dcterms:issued>
   <dc:type>journal article</dc:type>
   <dc:identifier>Holland R, McIntosh AL, Finucane OM, Mela V, Rubio-Araiz A, Timmons G, McCarthy SA, Gun'ko YK, Lynch MA. Inflammatory microglia are glycolytic and iron retentive and typify the microglia in APP/PS1 mice. Brain Behav Immun. 2018 Feb;68:183-196. doi: 10.1016/j.bbi.2017.10.017. Epub 2017 Oct 20. PMID: 29061364.</dc:identifier>
   <dc:identifier>https://hdl.handle.net/10630/40712</dc:identifier>
   <dc:identifier>10.1016/j.bbi.2017.10.017</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:rights>open access</dc:rights>
   <dc:publisher>Elsevier</dc:publisher>
</qdc:qualifieddc>
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