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Leptin inhibits neutrophil apoptosis in children via ERK/NF-κB-dependent pathways
Zhizhi Sun1, Stéphane Dragon, Allan Becker
1Department of Immunology, University of Manitoba, Winnipeg, Manitoba, Canada.
Insights
Leptin receptor is expressed on neutrophils in children, with lower expression in allergic asthmatics. Leptin promotes neutrophil survival via NF-κB and MAPK pathways, potentially increasing airway inflammation.
Area of Science:
- Immunology
- Cell Biology
- Pediatric Allergy
Background:
- Delayed neutrophil apoptosis is linked to chronic airway diseases.
- Leptin, an adipocyte hormone, regulates immune responses and cell survival.
- Increased serum leptin is observed during airway allergic reactions.
Purpose of the Study:
- To investigate leptin receptor expression and function in neutrophils from children.
- To determine the role of leptin in neutrophil apoptosis and survival pathways.
- To explore leptin's potential contribution to airway inflammation in pediatric populations.
Main Methods:
- Flow cytometry to detect leptin receptor expression on neutrophils from allergic asthmatic, allergic non-asthmatic, non-allergic asthmatic, and healthy children.
- Confocal microscopy to identify intracellular leptin receptor pools.
- Annexin-V/PI staining and caspase 3 activity assays to assess neutrophil apoptosis.
- Pharmacological inhibitors to investigate the involvement of MAPK and NF-κB pathways.
Main Results:
- Leptin receptor expression on neutrophils varied among children, with significantly lower expression in allergic asthmatics compared to healthy controls.
- An intracellular pool of leptin receptor was identified, which could be mobilized to the cell surface upon GM-CSF stimulation.
- Leptin demonstrated anti-apoptotic effects on neutrophils, mediated through the NF-κB and MEK1/2 MAPK pathways.
Conclusions:
- Neutrophils from children exhibit heterogeneous leptin receptor expression, influenced by allergic asthma status.
- Leptin's anti-apoptotic action on neutrophils, via specific signaling pathways, suggests a role in enhancing airway inflammation.
- These findings highlight leptin as a potential therapeutic target in pediatric airway diseases.
Introduction And Rationale:
Previous studies have shown that delayed neutrophil apoptosis is associated with chronic airway diseases. Leptin is an adipocyte-derived hormone that acts as a regulator of energy homeostasis and food intake. Emerging evidence suggests that leptin can regulate immune responses including the release of proinflammatory cytokines and protection of inflammatory cells from apoptosis. Serum leptin is increased during allergic reactions in the airways. However, the expression and function of leptin receptor in neutrophils isolated from children is not known.
Methods:
Flow cytometry was used to detect leptin receptor expression in neutrophils isolated from allergic asthmatic (n = 14), allergic non asthmatic (n = 21), non allergic asthmatic (n = 7) and healthy children (n = 23); confocal laser scanning microscopy combined with immunofluorescence was performed to detect intracellular pool of leptin receptor; Annexin-V/PI staining and caspase 3 activity was used to determine neutrophil survival. Pharmacological inhibitors were utilized to understand the role of MAPK and NF-κB pathway in leptin-induced neutrophil survival.
Results And Conclusion:
A heterogeneous leptin receptor expression was observed on neutrophils isolated from children. Neutrophils isolated from healthy children expressed more leptin receptor than those from allergic asthmatic (P<0.05) but not allergic non-asthmatic (P>0.05) or non-allergic asthmatic children (n = 7, P>0.05). Neutrophils isolated from children express an intracellular pool of leptin receptor that was mobilized to the cell surface upon GM-CSF stimulation. Finally, leptin exhibited anti-apoptotic properties on neutrophils via NF-κB and MEK1/2 MAPK pathway. Collectively, our data suggest that leptin may enhance airway inflammation by promoting neutrophil survival.
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