<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE344nnn/GSE344928/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE344928</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>CD84 Determines Differential Fates of Pro-fibrotic Macrophages [RNA-seq]</name><description>To define the transcriptional effects of CD84 engagement, bone marrow-derived macrophages (BMDMs) from wild-type and Cd84-knockout mice were stimulated with mouse recombinant CD84 (rCD84) and analyzed by bulk RNA sequencing. CD84 engagement induced inflammatory, chemotactic, survival, and adhesion-related gene programs in wild-type macrophages, whereas these responses were markedly reduced by Cd84 deletion. Pathway analysis highlighted cytokine activity, inflammatory responses, leukocyte chemotaxis, focal adhesion, TNF signaling, and JAK/STAT signaling. These findings establish CD84 as a key regulator of macrophage activation and pro-fibrotic transcriptional programming.</description><dates><publication>2026/09/25</publication></dates><accession>GSE344928</accession><cross_references><GSM>GSM9988143</GSM><GSM>GSM9988132</GSM><GSM>GSM9988142</GSM><GSM>GSM9988141</GSM><GSM>GSM9988140</GSM><GSM>GSM9988139</GSM><GSM>GSM9988138</GSM><GSM>GSM9988137</GSM><GSM>GSM9988136</GSM><GSM>GSM9988135</GSM><GSM>GSM9988134</GSM><GSM>GSM9988133</GSM><GPL>34290</GPL><GSE>344928</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>