{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["13"],"submitter":["Zheng LY"],"pubmed_abstract":["<h4>Background</h4>Dendritic cells are crucial in the development of sepsis, yet the effect of ribophagy on dendritic cell activation remains unclear. This study aimed to investigate the potential role of nuclear fragile X mental retardation-interacting protein 1 (NUFIP1), a selective autophagy receptor, on sequestering ribosomes in autophagosomes to maintain dendritic cell function during early stages of sepsis.<h4>Methods</h4>Splenic dendritic cells were isolated using CD11c<sup>+</sup> microbeads and treated with lipopolysaccharide. Sepsis models were generated using cecal ligation and puncture. Expression of dendritic cell surface molecules was detected using flow cytometry. Cytokine level was quantified using enzyme-linked immunosorbent assay kits. Laser scanning confocal microscopy w"],"journal":["Burns & trauma"],"pagination":["tkaf034"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC12448799"],"repository":["biostudies-literature"],"pubmed_title":["Nuclear fragile X mental retardation-interacting protein 1-mediated ribophagy regulates immune function of dendritic cells in polymicrobial sepsis."],"pmcid":["PMC12448799"],"pubmed_authors":["Wu MY","Yao RQ","Wei ST","Yao YM","Zheng LY","Zheng L","He PY","Dong N","Wu Y","Zhao PY","Duan Y"],"additional_accession":[]},"is_claimable":false,"name":"Nuclear fragile X mental retardation-interacting protein 1-mediated ribophagy regulates immune function of dendritic cells in polymicrobial sepsis.","description":"<h4>Background</h4>Dendritic cells are crucial in the development of sepsis, yet the effect of ribophagy on dendritic cell activation remains unclear. This study aimed to investigate the potential role of nuclear fragile X mental retardation-interacting protein 1 (NUFIP1), a selective autophagy receptor, on sequestering ribosomes in autophagosomes to maintain dendritic cell function during early stages of sepsis.<h4>Methods</h4>Splenic dendritic cells were isolated using CD11c<sup>+</sup> microbeads and treated with lipopolysaccharide. Sepsis models were generated using cecal ligation and puncture. Expression of dendritic cell surface molecules was detected using flow cytometry. Cytokine level was quantified using enzyme-linked immunosorbent assay kits. Laser scanning confocal microscopy w","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025","modification":"2026-06-03T15:39:32.079Z","creation":"2026-05-30T03:07:53.857Z"},"accession":"S-EPMC12448799","cross_references":{"pubmed":["40979900"],"doi":["10.1093/burnst/tkaf034"]}}