Work

Proinflammatory cytokines modify Ca2+ signaling and induce an apoptotic lipidome in murine small intestinal organoids

Year: 2026

Type: article

Abstract: Background Inflammatory bowel diseases (IBD) are associated with elevated levels of proinflammatory cytokines exerting a detrimental effect on the intestinal epithelium. Since contradictory studies regarding time-dependent actions on epithelial secretion exist, intestinal organoids were treated with a mix of proinflammatory cytokines. Methods Long-term (1–5 days) effects of a cytokine mix consisting of tumor necrosis factor α, interleukin-1β and interferon-γ on murine small intestinal epithelial organoids were investigated using live cell imaging, immunofluorescent staining, qPCR, scanning microprobe matrix-assisted laser desorption/ionization mass spectrometry imaging (AP-SMALDI MSI), and liquid-chromatography tandem mass spectrometry (UHPLC MS/MS). Results Treatment with the cytokine mix resulted in an enlarged organoid lumen. Stimulation of Cl – secretion seems to underly this swelling since it was inhibited by bumetanide, a blocker of Na + -K + -2Cl – cotransporters. Ca 2+ imaging experiments revealed that the cytokine mix time-dependently enhanced the response to carbachol, a Ca 2+ -dependent secretagogue, which would favor Ca 2+ -dependent Cl − secretion. This was concomitant with an upregulated gene expression of inositol-1,4,5-trisphosphate receptor type 1 (IP 3 R1) and stromal interaction molecule 2 (STIM2), which is involved in store-operated Ca 2+ entry. The cytokines induced apoptosis in organoids confirmed by an increase in caspase 3-immunopositive cells. Lipidomic analysis using UHPLC MS/MS revealed an upregulation of ceramides, sphingomyelins and ether-linked lipids within the epithelial cells. AP-SMALDI MSI showed an accumulation of ceramide-positive (apoptotic) cells within the organoid lumen. Conclusion Proinflammatory cytokines induce fluid secretion and transiently upregulate Ca 2+ signaling concomitant with the induction of an apoptotic lipidome in small intestinal organoids.

Source: Frontiers in Physiology

DOI: 10.3389/fphys.2026.1738447

Authors: Svenja Mareike Pauer, Alina Schindler, Parviz Ghezellou, Bernhard Spengler, Martin Diener, Jasmin Ballout

Institutions: Justus-Liebig-Universität Gießen, Goethe University Frankfurt

Language: English

Topic: Inflammatory Bowel Disease

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: gold

Estimated APC paid: $3,801