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Molecular mechanisms of leukocyte recruitment in postischemic liver microcirculation
Paul Kubes1, Derrice Payne, Richard C Woodman
1Immunology Research Group, Department of Physiology and Biophysics and Department of Medicine, University of Calgary Health Sciences Center, Calgary, Alberta, Canada T2N 4N1. pkubes@ucalgary.ca
Abstract:
Evidence shows that leukocyte recruitment into inflamed liver sinusoids does not require selectins, with one notable exception: ischemia-reperfusion (I/R). We used intravital microscopy to directly visualize the liver microcirculation during I/R and localized endotoxemia (liver superfused with lipopolysaccharide). General anti-selectin therapy (fucoidan) or anti-adhesion therapy with an antithrombin inhibitor (hirudin) was also used. Many neutrophils rolled and adhered in postsinusoidal vessels and sequestered in the sinusoids during I/R and local endotoxin superfusion. Although fucoidan blocked rolling in both forms of inflammation, leukocyte recruitment into sinusoids was only blocked in I/R. Adhesion was also inhibited in postischemic sinusoids with a second anti-adhesive agent (hirudin). Because liver I/R inevitably induces ischemia upstream in the intestine, anti-selectin therapy may prevent intestinal injury, which could prevent downstream liver inflammation. To test this hypothesis, we completely removed the intestine and rerouted blood flow from the superior mesenteric artery to the superior mesenteric vein. I/R was induced in the liver microcirculation, and many leukocytes rolled and adhered in postsinusoidal venules and adhered in sinusoids. Although fucoidan significantly reduced the rolling in postsinusoidal vessels, adhesion persisted in the sinusoids. Our data suggest that anti-adhesion therapy is effective in liver I/R in the sinusoids and postsinusoidal venules, perhaps in part due to its beneficial effect on the intestine.
Insights
Leukocyte recruitment in liver ischemia-reperfusion (I/R) inflammation relies on adhesion molecules, not selectins. Anti-adhesion therapy effectively targets leukocyte infiltration in liver sinusoids during I/R.
Area of Science:
- Immunology
- Hepatology
- Vascular Biology
Background:
- Leukocyte recruitment into liver sinusoids typically bypasses selectin-dependent mechanisms.
- Liver ischemia-reperfusion (I/R) presents a unique inflammatory exception where selectins may play a role.
Purpose of the Study:
- To investigate the role of selectins and adhesion molecules in leukocyte recruitment during liver I/R.
- To evaluate the efficacy of anti-selectin and anti-adhesion therapies in liver I/R models.
Main Methods:
- Intravital microscopy to visualize liver microcirculation during I/R and endotoxemia.
- Administration of anti-selectin (fucoidan) and anti-adhesion (hirudin) therapies.
- Surgical manipulation to isolate the liver from intestinal ischemia effects.
Main Results:
- Selectin-blocking therapy (fucoidan) inhibited neutrophil rolling but not adhesion in liver sinusoids during I/R.
- Anti-adhesion therapy (hirudin) effectively reduced leukocyte adhesion in postsinusoidal venules and sinusoids during I/R.
- Even after removing the intestine, leukocyte adhesion persisted in sinusoids during liver I/R, suggesting selectin-independent mechanisms.
Conclusions:
- Leukocyte recruitment in liver I/R is primarily mediated by selectin-independent adhesion pathways.
- Anti-adhesion therapy demonstrates significant efficacy in mitigating leukocyte infiltration in the liver during I/R.
- Targeting adhesion molecules offers a promising therapeutic strategy for liver I/R injury, potentially independent of upstream intestinal effects.