<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/003/SRR23310603/SRR23310603_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/002/SRR23310602/SRR23310602_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/002/SRR23310602/SRR23310602_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/003/SRR23310603/SRR23310603_1.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>College of Pharmacy, Pusan National University</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA930493</full_dataset_link><scientific_name>Mus musculus</scientific_name><long_description>Liver X receptor (LXR) is a critical regulator of cholesterol homeostasis, and inhibits TCR-induced proliferation by altering intracellular sterol metabolism. However, the mechanisms by which LXR regulates helper T cell subset differentiation in vivo remains unclear. Here we demonstrate here that LXR is a crucial regulator of follicular helper T (Tfh) cells in vivo. Both mixed bone marrow chimera and antigen-specific T cell adoptive co-transfer studies show a specific increase in Tfh cells among LXRβ-deficient CD4+ T cell population in response to immunization and LCMV infection. Mechanistically LXRβ-deficient Tfh cells express increased levels of TCF-1 but comparable levels of Bcl6, CXCR5, and PD-1 in comparison with LXRβ-sufficient Tfh cells. Loss of LXRβ confers inactivation of GSK3β induced by either AKT/ERK activation or Wnt/β-catenin pathway, leading to elevated TCF-1 expression in CD4+ T cells. Conversely, ligation of LXR represses TCF-1 expression and Tfh cell differentiation in both murine and human CD4+ T cells. Treatment with an LXR agonist significantly diminishes Tfh cells and the levels of antigen-specific IgG upon immunization. These findings unveil a novel cell-intrinsic regulatory function of LXR in Tfh cell differentiation via controlling GSK3β-TCF1 pathway, which might be a promising target for pharmacological intervention in Tfh-mediated diseases. Overall design: mRNA profiles of follicular helper T cells from wild type and Nr1h2-/- mice were generated by deep sequencing, singleplicate, using Illumina Truseq</long_description><tag>xref:PubMed:36802434</tag><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Liver X receptor controls follicular helper T cell differentiation via repression of TCF-1</name><description>Liver X receptor controls follicular helper T cell differentiation via repression of TCF-1</description><dates><last_updated>2025-09-24</last_updated><first_public>2023-02-07</first_public></dates><accession>PRJNA930493</accession><cross_references><GEO>GSE224303</GEO><taxon>10090</taxon><PubMed>36802434</PubMed></cross_references></HashMap>