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Stress-induced immunosuppression affecting immune response to Newcastle disease virus vaccine through "miR-155-CTLA-4"pathway in chickens
被引:4
|作者:
Wen, Jie
[1
]
Wu, Yiru
[1
]
Han, Jianwei
[1
]
Tian, Yufei
[1
]
Man, Chaolai
[1
]
机构:
[1] Harbin Normal Univ, Harbin, Peoples R China
来源:
关键词:
Chicken;
MiR-155;
CTLA-4;
gene;
Stress-induced immunosuppression;
Newcastle disease virus;
DEXAMETHASONE-INDUCED IMMUNOSUPPRESSION;
CTLA-4;
EXPRESSION;
MIR-155;
INHIBITION;
CHECKPOINT;
CD4(+);
CELLS;
D O I:
10.7717/peerj.14529
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
MiR-155 and CTLA-4 are important factors involved in the regulation of immune function. However, there is no report about their involvement in function regulation of stress-induced immunosuppression affecting immune response. In this study, the chicken model of stress-induced immunosuppression affecting immune response (simulation with dexamethasone and immunization with Newcastle disease virus (NDV) attenuated vaccine) was established, then the expression characteristics of miR-155 and CTLA-4 gene were analyzed at several key time points during the processes of stress-induced immunosuppression affecting NDV vaccine immune response at serum and tissue levels. The results showed that miR-155 and CTLA-4 were the key factors involved in stress-induced immunosuppression and NDV immune response, whose functions involved in the regulation of immune function were different in different tissues and time points, and 2 day post immunization (dpi), 5dpi and 21dpi were the possible key regulatory time points. CTLA-4, the target gene of miR-155, had significant game regulation relationships between them in various tissues, such as bursa of Fabricius, thymus and liver, indicating that miR-155-CTLA-4 pathway was one of the main mechanisms of their involvement in the regulations of stress -induced immunosuppression affecting NDV immune response. This study can lay the foundation for in-depth exploration of miR-155-CTLA-4 pathway involved in the regulation of immune function.
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页数:13
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