Ontology highlight
ABSTRACT: Objective
Neutrophil dysfunction is a hallmark of systemic lupus erythematosus (SLE), but its molecular basis remains unclear. This study explores transcriptional and post-transcriptional changes in low-density granulocytes (LDGs), a proinflammatory neutrophil subset expanded in SLE, focusing on NADPH oxidase (Nox) function and minor intron splicing.Methods
LDGs and normal-density neutrophils (NDGs) were isolated from SLE patients and healthy controls (HCs). CYBA (P22phox) expression was evaluated at transcript and protein levels. Nox activity was measured using luminol assays. Bulk RNA sequencing and rMATS software were used to assess alternative splicing, particularly of U12-type intron-containing genes.Results
CYBA expression was reduced in SLE LDGs (n=11) compar
SUBMITTER: Blanco LP
PROVIDER: S-EPMC12637451 | biostudies-literature | 2025 Nov
REPOSITORIES: biostudies-literature