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Study Design

Population
colonic epithelial cells and hypothermic hypoxia-induced NEC mice (both sexes)
Methods
In vitro and in vivo experiments using LPS-stimulated colonic epithelial cells and hypothermic hypoxia-induced NEC mice; L-cystine treatment; assessments of Th17/Treg balance, ferroptosis, IL-6 signaling, and conditioned medium experiments.
Funding
Unclear
Necrotizing enterocolitis (NEC) severely affects preterm infants with limited treatments. Although intestinal homeostasis dysfunction is considered a trigger for NEC, the key targets and mechanisms remain unclear. Using lipopolysaccharide-stimulated colonic epithelial cells and hypothermic hypoxia-induced NEC mice (both sexes), we demonstrate that the gut metabolite L-cystine alleviates intestinal inflammation by balancing Th17/Treg responses and inhibiting ferroptosis. Mechanistically, L-cystine directly targets KIF11 to suppress RC3H1 expression, blocking IL-6 transcripts through transcriptional modifications, thereby inhibiting IL-6 secretion and ferroptosis. Conditioned medium from L-cystine-treated cells inactivates IL-6/STAT3 signaling, reducing pro-inflammatory cytokine release and restoring Th17/Treg balance. Notably, microbiota colonization from NEC preterm infants exacerbates intestinal damage, an effect mitigated by L-cystine and IL-6/STAT3 inhibition. Thus, L-cystine attenuates NEC by suppressing ferroptosis in epithelial cells, restoring immune homeostasis, and preserving intestinal barrier integrity. Targeting intestinal metabolites represents a promising prophylactic and therapeutic strategy for NEC, addressing unmet clinical needs in neonatal intestinal injury management.

Research Insights

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