<HashMap><database>biostudies-literature</database><scores/><additional><submitter>von Bernhardi R</submitter><funding>Fondo Nacional de Desarrollo Científico y Tecnológico</funding><pagination>11378</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12692065</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(23)</volume><pubmed_abstract>Ageing results in an increased microglial activation and neuroinflammation. We are interested in assessing ageing-dependent changes in the amount and fractalkine (CX3CL1) proteoforms participating in neuron-microglia crosstalk that could be involved in microglia activation. We analysed age-dependent changes in CX3CL1, CX3CR1, and TGFβ mRNAs using RT-qPCR and CX3CL1 proteoforms using Western blot, in 3 to 20-month-old WT mice and an inflammatory mouse model (SRA&lt;sup>-/-&lt;/sup>) treated with 0.5 mg/kg of intraperitoneal LPS, 2 ng of intrathecal TGFβ, or a vehicle. CX3CL1, CX3CR1, and TGFβ were affected by ageing. CX3CL1 mRNA was similar in young and adult mice but decreased by 52% in >20-month-old mice; adult mice showed a 3-fold increase in 70 kDa soluble CX3CL1. CX3CR1 showed a progressive </pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Age-Related Changes in Neuron-Microglia Interaction Mediated by Fractalkine Under Inflammatory Conditions.</pubmed_title><pmcid>PMC12692065</pmcid><funding_grant_id>1221028</funding_grant_id><pubmed_authors>Godoy G</pubmed_authors><pubmed_authors>Eugenin J</pubmed_authors><pubmed_authors>von Bernhardi R</pubmed_authors><pubmed_authors>Metz C</pubmed_authors><pubmed_authors>Cortes F</pubmed_authors><pubmed_authors>Narea C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Age-Related Changes in Neuron-Microglia Interaction Mediated by Fractalkine Under Inflammatory Conditions.</name><description>Ageing results in an increased microglial activation and neuroinflammation. We are interested in assessing ageing-dependent changes in the amount and fractalkine (CX3CL1) proteoforms participating in neuron-microglia crosstalk that could be involved in microglia activation. We analysed age-dependent changes in CX3CL1, CX3CR1, and TGFβ mRNAs using RT-qPCR and CX3CL1 proteoforms using Western blot, in 3 to 20-month-old WT mice and an inflammatory mouse model (SRA&lt;sup>-/-&lt;/sup>) treated with 0.5 mg/kg of intraperitoneal LPS, 2 ng of intrathecal TGFβ, or a vehicle. CX3CL1, CX3CR1, and TGFβ were affected by ageing. CX3CL1 mRNA was similar in young and adult mice but decreased by 52% in >20-month-old mice; adult mice showed a 3-fold increase in 70 kDa soluble CX3CL1. CX3CR1 showed a progressive </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-05-26T11:08:45.79Z</modification><creation>2026-05-24T03:11:29.993Z</creation></dates><accession>S-EPMC12692065</accession><cross_references><pubmed>41373544</pubmed><doi>10.3390/ijms262311378</doi></cross_references></HashMap>