Related Experiment Video
Updated: Jan 24, 2026

Intravenous Endotoxin Challenge in Healthy Humans: An Experimental Platform to Investigate and Modulate Systemic Inflammation
Published on: May 16, 2016
Primed PMNs in healthy mouse and human circulation are first responders during acute inflammation
Noah Fine1, Oriyah Barzilay1, Chunxiang Sun1
1Matrix Dynamics Group, Faculty of Dentistry, University of Toronto, Toronto, ON, Canada.
Abstract:
Polymorphonuclear neutrophils (PMNs) are the most abundant circulating leukocytes, and the first cells recruited to sites of tissue inflammation. Using a fixation method to preserve native CD marker expression prior to immunophenotyping, we identified a distinct population of "primed for recruitment" PMNs in healthy mouse and human blood that has high expression of adhesion and activation markers compared with the bulk resting-state PMNs. In response to acute tissue inflammation, primed PMNs (pPMNs) were rapidly depleted from the circulation and recruited to the tissue. One hour after acute peritoneal insult, pPMNs became the dominant PMN population in bone marrow (BM) and blood, returning to baseline levels with resolution of inflammation. PMN priming was induced by the granulopoietic factors granulocyte-macrophage-colony-stimulating factor (GM-CSF) and granulocyte-colony-stimulating factor (G-CSF). High levels of pPMNs were observed in neutropenic mice and in pediatric neutropenic patients who were resistant to infection, highlighting an important role of this population in innate immune function.
Insights
Researchers discovered a distinct population of "primed for recruitment" polymorphonuclear neutrophils (PMNs) that are rapidly deployed to inflammation sites. These primed PMNs play a crucial role in the innate immune response.
Area of Science:
- Immunology
- Cell Biology
- Hematology
Background:
- Polymorphonuclear neutrophils (PMNs) are key immune cells involved in inflammation.
- Existing methods may not fully capture the functional state of PMNs in circulation.
Purpose of the Study:
- To identify and characterize a distinct subset of PMNs with enhanced recruitment potential.
- To investigate the role of these primed PMNs in innate immunity and response to inflammation.
Main Methods:
- Utilized a novel fixation method to preserve native CD marker expression on PMNs.
- Employed immunophenotyping to distinguish between resting and primed PMN populations.
- Studied PMN dynamics in mouse models of acute inflammation and in human subjects.
Main Results:
- Identified a population of "primed for recruitment" PMNs (pPMNs) with high adhesion and activation markers.
- Observed rapid depletion of pPMNs from circulation and recruitment to inflamed tissues.
- Found that granulopoietic factors (GM-CSF, G-CSF) induce PMN priming.
- Noted elevated pPMN levels in neutropenic individuals resistant to infection.
Conclusions:
- A distinct, primed PMN population exists and is crucial for effective innate immunity.
- PMN priming is a regulated process influenced by specific growth factors.
- Understanding pPMNs offers insights into immune defense mechanisms, particularly in neutropenic conditions.
Related Concept Videos
Inflammation
Fetal Circulation
Two umbilical arteries transport blood from the fetus to the placenta. At the placenta, the blood absorbs oxygen and nutrients while simultaneously eliminating waste products. This oxygen-enriched and nutrient-rich blood then returns to the fetus through one...
Coronary Circulation
Coronary circulation begins at the base of the aorta, where two main arteries arise—the left and right coronary arteries. These arteries encircle the heart in the coronary sulcus and supply the...
Overview of Pulmonary Circulation
The process begins with the right ventricle of the heart pumping deoxygenated blood into the pulmonary trunk. This large vessel extends about 5 centimeters before splitting into the left and right pulmonary arteries. These arteries...
Overview of Systemic and Pulmonary Circulation
The oxygenated blood is sent...
Bioavailability Study Design: Healthy Subjects Versus Patients

