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Updated: Aug 9, 2026

A Microphysiological System to Study Leukocyte-Endothelial Cell Interaction during Inflammation
Published on: December 9, 2021
Leukocyte-endothelial interactions via ICAM-1 are detrimental in polymicrobial sepsis
Martijn van Griensven1, Christian Probst, Katrin Müller
1Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, Donaueschingenstrasse 13, A-1200 Vienna, Austria. Martijn.van.Griensven@ibitrauma.org
Abstract:
Intercellular adhesion molecule 1 (ICAM-1) plays an important role in the transmigration of polymorphonuclear neutrophils (PMN) in sepsis. Moreover, the transmigration rate of leukocytes from the blood via endothelial adhesion molecules into tissues correlates with the severity of multi organ failure. We examined the effect of the deletion of the ICAM-1 gene in polymicrobial sepsis using a cecal ligation and puncture (CLP) sepsis model in mice. Twenty male ICAM-1 knockout (KO) mice and 20 wild-type (WT) male C57BL/6 mice were studied. CLP was performed. At several time points during a 96-hour postoperative observation period, we measured mortality, body weight, and temperature. The delayed type of hypersensitivity (DTH) reaction was determined by pinna swelling after sensitization with 50 microL of dinitrofluorobenzene (DNFB) 1%. Lymphocyte subpopulations (CD4, CD8, and CD56) and cytokines [tumor necrosis factor-alpha (TNF-alpha), interleukin-1beta (IL-1beta), interleukin-6 (IL-6), and interleukin-10 (IL-10)] were measured using flow cytometry and ELISA testing, respectively. Also, a histologic examination of the liver and lung was performed. CLP-induced mortality was lower in the ICAM-1 group compared to normal mice (5% vs 45.0%). So were the ratios of lymphocyte subpopulations in the KO versus the WT group [CD4: 16.4 +/- 1.6% vs 25.7 +/- 4.7%; CD8: 18.3 +/- 1.4% vs 34.9 +/- 2.9%; natural killer (NK) cells: 5.6 +/- 0.3% vs 49.5 +/- 0.7%; P < 0.01]. And also the cytokine blood levels of the KO mice were significantly lower versus the WT mice (TNF-alpha: 67.2 +/- 42.2 vs 823.9 +/- 170.5 pg/mL; IL-1beta: 5.9 +/- 0.9 vs 296.2 +/- 66.2 pg/mL; IL-6: 223.1 +/- 48.8 vs 3062.5 +/- 1222.8 pg/mL; IL-10: 34.6 +/- 5.8 vs 1565.6 +/- 448.8 pg/mL; P < 0.01). With respect to the histology, significantly less leukocyte invasion and organ damage (eg, hydropic degeneration) were present in the ICAM-1-/- group compared to controls in liver and lung tissues. The DTH reaction was significantly decreased in ICAM-1-/- mice versus WT mice (0.34 vs 0.41 mm; P < 0.05). Our results demonstrate a significant reduction of mortality after septic challenge in ICAM-1-/- mice compared to normal mice. This is associated with a decrease in lymphocyte subpopulations, cytokine levels, and DTH type 4 reaction, possibly reflecting an overall attenuation of the immune system.
Insights
Mice lacking the ICAM-1 gene showed significantly reduced mortality in a sepsis model. This was linked to lower immune cell activity and inflammatory markers, suggesting ICAM-1 plays a key role in sepsis severity.
Area of Science:
- Immunology
- Pathophysiology
- Sepsis Research
Background:
- Intercellular Adhesion Molecule 1 (ICAM-1) is crucial for leukocyte transmigration in sepsis.
- Leukocyte transmigration correlates with multi-organ failure severity.
- The role of ICAM-1 gene deletion in polymicrobial sepsis requires further investigation.
Purpose of the Study:
- To investigate the impact of ICAM-1 gene deletion on mortality and immune responses in a murine model of polymicrobial sepsis.
- To evaluate the effect of ICAM-1 deficiency on leukocyte subpopulations, cytokine levels, and organ damage.
Main Methods:
- A cecal ligation and puncture (CLP) sepsis model was used in ICAM-1 knockout (KO) and wild-type (WT) mice.
- Mortality, body weight, temperature, delayed-type hypersensitivity (DTH) reaction, lymphocyte subpopulations, and cytokine levels were measured.
- Histological examination of liver and lung tissues was performed.
Main Results:
- Mortality was significantly lower in ICAM-1 KO mice compared to WT mice (5% vs 45.0%).
- KO mice exhibited reduced lymphocyte subpopulations (CD4, CD8, NK cells) and lower levels of pro-inflammatory cytokines (TNF-alpha, IL-1beta, IL-6, IL-10).
- Histology revealed less leukocyte invasion and organ damage in KO mice, with a decreased DTH reaction.
Conclusions:
- ICAM-1 gene deletion significantly reduces mortality in a murine sepsis model.
- The reduced mortality is associated with an attenuated immune response, including decreased lymphocyte counts, cytokine levels, and DTH reaction.
- These findings highlight ICAM-1's critical role in sepsis pathogenesis and suggest it as a potential therapeutic target.
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