<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Salas-Gallardo GA</submitter><funding>Consejo Nacional de Ciencia y Tecnología</funding><funding>Dirección General de Asuntos del Personal Académico, Universidad Nacional Autónoma de México</funding><pagination>e0297576</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10919594</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(3)</volume><pubmed_abstract>The Peritumoral Brain Zone (PBZ) contributes to Glioblastoma (GBM) relapse months after the resection of the original tumor, which is influenced by a variety of pathological factors. Among those, microglia are recognized as one of the main regulators of GBM progression and probably relapse. Although microglial morphology has been analyzed inside GBM and its immediate surroundings, it has not been objectively characterized throughout the PBZ. Thus, we aimed to perform a thorough characterization of microglial morphology in the PBZ and its likely differentiation not just from the tumor-associated microglia but from control tissue microglia. For this purpose, Sprague Dawley rats were intrastriatally implanted with C6 cells to induce a GBM formation. Gadolinium-based magnetic resonance imaging</pubmed_abstract><journal>PloS one</journal><pubmed_title>Morphological differentiation of peritumoral brain zone microglia.</pubmed_title><pmcid>PMC10919594</pmcid><funding_grant_id>A1-S-7540</funding_grant_id><funding_grant_id>IG200521</funding_grant_id><pubmed_authors>Pena-Ortega F</pubmed_authors><pubmed_authors>Robles-Gomez AA</pubmed_authors><pubmed_authors>Salas-Gallardo GA</pubmed_authors><pubmed_authors>Lorea-Hernandez JJ</pubmed_authors><pubmed_authors>Del Campo CC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Morphological differentiation of peritumoral brain zone microglia.</name><description>The Peritumoral Brain Zone (PBZ) contributes to Glioblastoma (GBM) relapse months after the resection of the original tumor, which is influenced by a variety of pathological factors. Among those, microglia are recognized as one of the main regulators of GBM progression and probably relapse. Although microglial morphology has been analyzed inside GBM and its immediate surroundings, it has not been objectively characterized throughout the PBZ. Thus, we aimed to perform a thorough characterization of microglial morphology in the PBZ and its likely differentiation not just from the tumor-associated microglia but from control tissue microglia. For this purpose, Sprague Dawley rats were intrastriatally implanted with C6 cells to induce a GBM formation. Gadolinium-based magnetic resonance imaging</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2026-06-12T10:10:08.706Z</modification><creation>2025-04-04T12:34:55.537Z</creation></dates><accession>S-EPMC10919594</accession><cross_references><pubmed>38451958</pubmed><doi>10.1371/journal.pone.0297576</doi></cross_references></HashMap>