Alterations in thymocyte populations under conditions of endotoxin tolerance.
10.1097/CM9.0000000000001598
- VernacularTitle:Alterations in thymocyte populations under conditions of endotoxin tolerance
- Author:
Yi-Jing TAO
1
;
Juan-Juan ZHAO
2
;
Li-Hua RAO
1
;
Song YANG
1
;
Guo-Liang ZHANG
1
;
Meng-Meng GUO
2
;
Chao CHEN
2
;
Lin XU
2
Author Information
1. Department of Laboratory Medicine, Jiangxi Hospital of Integrated Chinese and Western Medicine, Nanchang, Jiangxi 330009, China.
2. Department of Immunology, Zunyi Medical University, Zunyi, Guizhou 563000, China.
- Publication Type:Journal Article
- MeSH:
Animals;
CD4-Positive T-Lymphocytes;
Cell Differentiation;
Endotoxins/toxicity*;
Flow Cytometry;
Mice;
Signal Transduction;
Thymocytes;
Thymus Gland
- From:
Chinese Medical Journal
2021;134(15):1855-1865
- CountryChina
- Language:English
-
Abstract:
BACKGROUND:Endotoxin tolerance (ET) is a protective phenomenon in which pre-treatment with a tolerance dose of lipopolysaccharide (LPS) leads to dramatically elevated survival. Accumulating evidence has shown that peripheral T cells contribute to the induction of ET. However, what happens to T cell development in the thymus under ET conditions remains unclear. The purpose of this study was to analyze the alterations in thymocyte populations (double-positive [DP] and single-positive [SP] cells) under ET conditions.
METHODS:Mice were intraperitoneally injected with LPS at a concentration of 5 mg/kg to establish an LPS tolerance model and were divided into two groups: a group examined 72 h after LPS injection (72-h group) and a group examined 8 days after LPS injection (8-day group). Injection of phosphate-buffered saline was used as a control (control group). Changes in thymus weight, cell counts, and morphology were detected in the three groups. Moreover, surface molecules such as CD4, CD8, CD44, CD69, and CD62L were analyzed using flow cytometry. Furthermore, proliferation, apoptosis, cytokine production, and extracellular signal-regulated kinase (ERK) pathway signaling were analyzed in thymocyte populations. The polymorphism and length of the T-cell receptor (TCR) β chain complementarity-determining region 3 (CDR3) were analyzed using capillary electrophoresis DNA laser scanning analysis (ABI 3730).
RESULTS:Thymus weight and cell counts were decreased in the early stage but recovered by the late stage in a murine model of LPS-induced ET. Moreover, the proportions of DP cells (control: 72.130 ± 4.074, 72-h: 10.600 ± 3.517, 8-day: 84.770 ± 2.228), CD4+ SP cells (control: 15.770 ± 4.419, 72-h: 44.670 ± 3.089, 8-day: 6.367 ± 0.513), and CD8+ SP cells (control: 7.000 ± 1.916, 72-h: 34.030 ± 3.850, 8-day: 5.133 ± 0.647) were obviously different at different stages of ET. The polymorphism and length of TCR β chain CDR3 also changed obviously, indicating the occurrence of TCR rearrangement and thymocyte diversification. Further analysis showed that the expression of surface molecules, including CD44, CD69, and CD62L, on thymocyte populations (DP and SP cells) were changed to different degrees. Finally, the proliferation, apoptosis, cytokine production, and ERK pathway signaling of thymocyte populations were changed significantly.
CONCLUSION:These data reveal that alterations in thymocyte populations might contribute to the establishment of ET.
