<HashMap><database>biostudies-arrayexpress</database><scores/><additional><omics_type>Metabolomics</omics_type><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><submitter>Aymeric Silvin</submitter><instrument_platform>BD Rhapsody</instrument_platform><instrument_platform>Illumina HiSeq 4000</instrument_platform><study_type>RNA-seq of coding RNA from single cells</study_type><organism>Mus musculus</organism><species>Mus musculus</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-14797</full_dataset_link><description>Microglia are brain-resident macrophages critical for cerebral development, function and homeostasis. During development, yolk-sac-derived microglial progenitors colonize and populate the brain following a well-defined spatiotemporal pattern. However, the mechanisms driving microglial colonization and proliferation are largely unknown. Herein, using scRNA-seq of conditional inactivation of Colony Stimulating Factor 1 (Csf1), we revealed that embryonic cortical microglia critically rely on neural Csf1, mainly produced by cortical progenitors but also by post-mitotic neurons, and that the action of Csf1 is local, dose-dependent and transient. Alongside, intrinsic Csf1 expressed by ATM contributed to their sustained proliferation at developmental hotspots.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Nucleic Acid Extraction - cells were captured and processed in a two run. Run 1 = Sample 1 ; Run 2 = Sample 2. Four sample tags were used in Run 1 (comprising 2 mix, and 2 wild type), pooled using the BDTM Ms Single Cell Sample Multiplexing Kit (Cat No: 633793). Six sample tags were used in Run 2 (comprising 1 mix, 2 wild type and 3 EMX1creCSF1flox)</sample_protocol><sample_protocol>Sample Collection - CD45+ cells were enriched using CD45 microbeads from Miltenyi (Cat# 130-052-301) and the Automacs using possel function.</sample_protocol><sample_protocol>Library Construction - The sample was processed according to the BD Rhapsody™ Whole Transcriptom protocol</sample_protocol><sample_protocol>Sequencing - ome Analysis (WTA) Amplification Kit (Cat No: 633801) and the BD Rhapsody™ Whole Transcriptome Analysis (WTA) Reagent Kit (Cat No: 665915). The library was then subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) with 20% PhiX spike in. Over 3 753 million reads were sequenced.</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><pubmed_authors>Aymeric Silvin</pubmed_authors></additional><is_claimable>false</is_claimable><name>Microglial colonization is shaped by intrinsic and extrinsic CSF-1 during early forebrain development</name><description>Microglia are brain-resident macrophages critical for cerebral development, function and homeostasis. During development, yolk-sac-derived microglial progenitors colonize and populate the brain following a well-defined spatiotemporal pattern. However, the mechanisms driving microglial colonization and proliferation are largely unknown. Herein, using scRNA-seq of conditional inactivation of Colony Stimulating Factor 1 (Csf1), we revealed that embryonic cortical microglia critically rely on neural Csf1, mainly produced by cortical progenitors but also by post-mitotic neurons, and that the action of Csf1 is local, dose-dependent and transient. Alongside, intrinsic Csf1 expressed by ATM contributed to their sustained proliferation at developmental hotspots.</description><dates><release>2025-09-18T00:00:00Z</release><modification>2025-09-18T01:02:33.788Z</modification><creation>2025-01-29T17:33:27.138Z</creation></dates><accession>E-MTAB-14797</accession><cross_references><ENA>ERP168786</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0005684</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>