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Updated: Dec 20, 2025

A Microphysiological System to Study Leukocyte-Endothelial Cell Interaction during Inflammation
Published on: December 9, 2021
Leukocyte-Endothelium Interaction Is Associated with Fat Mass in Children
Miguel Martí-Masanet1, Pilar Codoñer-Franch2, Samuel Orden3
1Department of Pediatrics, University Hospital Dr. Peset, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region (FISABIO), Valencia, Spain.
Insights
Children with overweight or obesity exhibit altered leukocyte-endothelium interactions, characterized by reduced rolling velocity and increased rolling flux and adhesion. These changes are linked to excess fat mass and may promote early atherosclerosis development.
Area of Science:
- Pediatric Endocrinology
- Cardiovascular Research
- Immunology
Background:
- Childhood obesity is a growing public health concern.
- Obesity is associated with chronic inflammation and an increased risk of cardiovascular disease.
- Leukocyte-endothelium interaction is a critical early step in atherogenesis.
Purpose of the Study:
- To investigate leukocyte-endothelium interactions in children with overweight or obesity.
- To assess whether excess adiposity influences the initial phases of atherosclerosis development in pediatric populations.
Main Methods:
- Prospective study of 77 children (7-16 years), including 47 overweight/obese and 30 normal weight.
- Isolation of polymorphonuclear neutrophils (PMNs) and peripheral blood mononuclear cells.
- Analysis of leukocyte-endothelium interactions using flow chamber microscopy, measuring rolling velocity, flux, and adhesion.
Main Results:
- Overweight/obese children showed significantly reduced PMN and mononuclear cell rolling velocity.
- Increased rolling flux and adhesion of leukocytes were observed in the overweight/obesity group compared to controls.
- Fat mass index was the primary predictor of leukocyte adhesion, and C-reactive protein correlated with altered interactions.
Conclusions:
- Excess fat mass in children activates leukocyte-endothelium interactions.
- These altered interactions may contribute to the early development of atherosclerosis in obese children.
- Findings highlight the importance of managing childhood obesity to mitigate cardiovascular risk.
Objective:
To study leukocyte-endothelium interaction, a measure of the initial phase of atheromatosis, in children with overweight or obesity.
Study Design:
A prospective study was conducted in 77 children aged 7-16 years; 47 were children with overweight/obesity and 30 were normal weight. Polymorphonuclear neutrophils (PMNs) and peripheral blood mononuclear cells were isolated from venous blood samples and the interaction of leukocytes over a monolayer of human umbilical vein endothelial cells was analyzed using flow chamber microscopy. The variables studied included leukocyte rolling velocity, rolling flux, and adhesion to endothelial cells. These were compared between children with overweight/obesity and control children. Correlation between the measures of leukocyte-endothelium interaction and anthropometric and biochemical variables was evaluated.
Results:
In comparison with normal weight children, the PMNs and peripheral blood mononuclear cells of the overweight/obesity group showed a reduction in rolling velocity (P = .000 and P = .001, respectively) and an increase in rolling flux (P = .001 and P = .004), and adhesion (P = .003 and P = .002). The homeostasis model of insulin resistance was correlated inversely with rolling velocity and positively with rolling flux in PMNs. C-reactive protein was correlated positively with rolling flux and adhesion in both types of leucocytes. Fat mass index was correlated with all measures of leukocyte-endothelial interaction and proved to be the main predictor of leukocyte adhesion in the multiple regression analysis (P = .001 for PMNs and P = .006 for peripheral blood mononuclear cells).
Conclusions:
Excess fat mass in children is related to the activation of the leukocyte-endothelium interaction, potentially contributing to the development of atherosclerosis.
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