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In vitro lipopolysaccharide treatment alters regulatory T cell properties in chickens
Revathi Shanmugasundaram1, Ramesh K Selvaraj
1Department of Animal Sciences, Ohio Agricultural Research and Development Center, Wooster, OH 44691, United States.
Abstract:
The objective of this study was to identify the effect of in vitro lipopolysaccharide (LPS) treatment on regulatory T cells (Tregs) from chickens. Tregs had approximately 30-fold higher TLR 2-type 2 and six-fold higher TLR 4 mRNA content than CD4+CD25- cells. Tregs were treated with either 0 or 1 μg/ml LPS for 0, 2, and 4d. LPS treatment increased the IL-2 mRNA amount in Tregs at 2 and 4d post-LPS treatment. LPS treatment increased the IL-10 mRNA amount in Tregs at 4d post-LPS treatment. The total live cell numbers were approximately two-fold higher at 2d and three-fold higher at 4d in the 1 μg/ml LPS-treated groups than in the 0 μg LPS-treated controls. LPS treatment abrogated suppressive properties of Tregs at 2d post-LPS treatment. At 4d post-LPS treatment, Tregs became supersuppressive. In conclusion, chicken Tregs are differentially activated to facilitate immune response during the early stage of inflammation and to facilitate immune suppression at a later stage of inflammation.
Insights
Lipopolysaccharide (LPS) treatment alters chicken regulatory T cells (Tregs). Initially, LPS enhances immune response, but later induces supersuppression, demonstrating differential activation during inflammation.
Area of Science:
- Immunology
- Cell Biology
- Veterinary Science
Background:
- Regulatory T cells (Tregs) play a crucial role in maintaining immune homeostasis.
- Toll-like receptors (TLRs) are key components of the innate immune system, recognizing pathogen-associated molecular patterns.
- Understanding avian immune responses is vital for poultry health and disease management.
Purpose of the Study:
- To investigate the in vitro effects of lipopolysaccharide (LPS) on chicken regulatory T cells (Tregs).
- To determine how LPS influences Treg function, including cytokine production and suppressive capacity.
Main Methods:
- Chicken Tregs were isolated and treated with varying concentrations of LPS (0 or 1 μg/ml) over time (0, 2, and 4 days).
- Quantitative real-time PCR was used to measure mRNA levels of TLRs, IL-2, and IL-10.
- Cell proliferation assays and functional suppression assays were performed.
Main Results:
- Tregs exhibited higher mRNA expression of TLR 2 and TLR 4 compared to CD4+CD25- cells.
- LPS treatment upregulated IL-2 mRNA at 2 and 4 days, and IL-10 mRNA at 4 days.
- LPS exposure led to increased Treg proliferation and initially abrogated, then enhanced, Treg suppressive function, resulting in supersuppression by day 4.
Conclusions:
- Chicken Tregs demonstrate dynamic functional changes in response to LPS stimulation.
- Early-stage LPS treatment promotes immune activation, while later stages induce potent immune suppression.
- These findings highlight the differential roles of Tregs in managing inflammation in chickens.
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