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Published on: August 17, 2022
Increased CD11b+ cells and Interleukin-1 (IL-1) alpha levels during cardiomyopathy induced by chronic adrenergic
Jeremy Ben-Shoshan1, Ayman Jubran1, Ran Levy1
1Department of Cardiology, Tel Aviv Sourasky Medical Center, affiliated with the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Insights
Systemic CD11b+ cells and IL-1 signaling are linked to cardiomyopathy from chronic adrenergic stimulation. This suggests a role for immune system modulation in heart disease development.
Area of Science:
- Cardiovascular Research
- Immunology
- Cell Biology
Background:
- Systemic CD11b+ cells are implicated in various cardiac conditions, including chronic heart failure.
- Understanding the role of immune cells in cardiac disease is crucial for developing new therapies.
Purpose of the Study:
- To investigate the levels of circulating CD11b+ cells and pro-inflammatory cytokines in rats with cardiomyopathy induced by chronic adrenergic stimulation.
- To explore the relationship between systemic immune markers and cardiac dysfunction.
Main Methods:
- Male Lewis rats received low-dose isoproterenol for 3 months to induce cardiomyopathy.
- Echocardiography assessed cardiac function, flow cytometry quantified CD11b+ cells, and cytokine arrays measured inflammatory markers.
- Real-time PCR analyzed cardiac IL-1 receptor expression, and histology evaluated fibrosis and inflammation.
Main Results:
- Isoproterenol induced cardiac hypertrophy, fibrosis, and dysfunction, with increased heart rate and heart weight-to-body weight ratio.
- CD11b+ cells accumulated in the spleen, but cardiac inflammation was not observed.
- Elevated serum IL-1 alpha and cardiac IL-1 receptor type 2 overexpression correlated with cardiac dysfunction.
Conclusions:
- Systemic CD11b+ cell levels and IL-1 signaling pathways are associated with cardiomyopathy induced by chronic adrenergic stimulation.
- These findings highlight the potential involvement of systemic immunomodulation in this type of cardiomyopathy.
- Further research is warranted to elucidate the precise role of systemic immunity in cardiac disease.
Background:
Systemic CD11b+ cells have been associated with several cardiac diseases, such as chronic heart failure.
Objectives:
To assess the levels of circulating CD11b+ cells and pro-inflammatory cytokines in cardiomyopathy induced by chronic adrenergic stimulation.
Methods:
Male Lewis rats were injected with low doses of isoproterenol (isoprel) for 3 months. Cardiac parameters were tested by echocardiography. The percentage of CD11b+ cells was tested by flow cytometry. The levels of inflammatory cytokines in the sera were determined by an inflammation array, and the expression levels of cardiac interleukin-1 (IL-1) receptors were analyzed by real-time polymerase chain reactions. Cardiac fibrosis and inflammation were determined by histological analysis.
Results:
Chronic isoprel administration resulted in increased heart rate, cardiac hypertrophy, elevated cardiac peri-vascular fibrosis, reduced fractional shortening, and increased heart weight per body weight ratio compared to control animals. This clinical presentation was associated with accumulation of CD11b+ cells in the spleen with no concomitant cardiac inflammation. Cardiac dysfunction was also associated with elevated sera levels of IL-1 alpha and over expression of cardiac IL-1 receptor type 2.
Conclusions:
CD11b+ systemic levels and IL-1 signaling are associated with cardiomyopathy induced by chronic adrenergic stimulation. Further studies are needed to define the role of systemic immunomodulation in this cardiomyopathy.
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