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Updated: May 5, 2026

Isolation and Characterization of Dendritic Cells and Macrophages from the Mouse Intestine
Published on: May 21, 2012
Interleukin 12 is expressed and actively released by Crohn's disease intestinal lamina propria mononuclear cells
G Monteleone1, L Biancone, R Marasco
1Dipartimento di Medicina Sperimentale e Clinica, Università di Reggio Calabria, Catanzaro, Italy.
Insights
Crohn's disease (CD) patients show increased expression of interleukin (IL)-12 in intestinal cells. This bioactive IL-12 release is significantly higher in CD compared to ulcerative colitis (UC), suggesting it differentiates the two conditions.
Area of Science:
- Immunology
- Gastroenterology
- Molecular Biology
Background:
- Cell-mediated immunity is a hallmark of Crohn's disease (CD).
- Interleukin (IL)-12, a cytokine produced by phagocytes, stimulates T-cell production of interferon (IFN)-gamma.
- The role of IL-12 in CD pathogenesis requires further investigation.
Purpose of the Study:
- To determine if lamina propria mononuclear cells (LPMCs) from CD patients express and release bioactive IL-12.
- To compare IL-12 expression and release in CD LPMCs versus those from ulcerative colitis (UC) patients and healthy controls.
Main Methods:
- Isolation of LPMCs from CD patients, UC patients, and controls.
- Detection of IL-12 subunit mRNA using reverse-transcription polymerase chain reaction.
- Quantification of bioactive IL-12 in LPMC supernatants via enzyme-linked immunosorbent assay (ELISA).
Main Results:
- IL-12 mRNA transcripts were significantly more prevalent in LPMCs from CD patients (11/13) compared to UC (1/9) and controls (1/13).
- Bioactive IL-12 was detected in unstimulated CD LPMC supernatants and its release was enhanced by mitogens.
- Significant IL-12 production was largely absent in unstimulated UC and control LPMCs, with lower induced levels in UC compared to CD.
Conclusions:
- Intestinal tissues in CD exhibit IL-12 gene expression.
- LPMCs from CD patients demonstrate an augmented capacity for releasing bioactive IL-12.
- The differential expression and release of bioactive IL-12 may serve as a distinguishing factor between CD and UC.
Background & Aims:
Cell-mediated immunity is a feature of Crohn's disease (CD). The heterodimer interleukin (IL)-12, produced by phagocytes, induces T-cell cytokines, primarily interferon (IFN)-gamma. This study examined whether CD lamina propria mononuclear cells (LPMCs) express and release bioactive IL-12.
Methods:
LPMCs were isolated from 13 patients with CD, 9 with ulcerative colitis (UC), and 13 controls. Messenger RNA for p40 and p35 IL-12 subunits was evaluated by reverse-transcription polymerase chain reaction. IL-12 was measured by enzyme-linked immunosorbent assay in LPMC culture supernatants. The INF-gamma-inducing effect of unstimulated LPMC supernatants was evaluated.
Results:
Messenger RNA for both IL-12 subunits was detected in LPMCs of 11 of 13 patients with CD, 1 of 9 patients with UC, and 1 of 13 controls (P < 0.001). IL-12 was measured (10.5 +/- 2 pg/mL at 24 hours) in unstimulated CD LPMCs and was enhanced by pokeweed mitogen, lipopolysaccharide, and staphylococcal enterotoxin B. No IL-12 was detectable in 8 of 9 patients with UC and 12 of 13 control-unstimulated LPMCs. IL-12 induced by pokeweed mitogen and staphylococcal enterotoxin B in UC was lower than in CD and did not differ from controls. An IFN-gamma-inducing effect was restricted to unstimulated CD LPMC supernatants and was inhibited by an anti-IL-12 antibody in a dose-dependent fashion.
Conclusions:
IL-12 transcripts are expressed in CD intestinal tissues. CD LPMCs are up-regulated in their capability of releasing bioactive IL-12. Expression and release of bioactive IL-12 seem to differentiate CD from UC.
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