Anti-CD200 attenuates concanavalin A induced hepatitis via modulating the imbalance of CD4 + T lymphocyte differentiation in mice.
AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH(2018)
摘要
Hepatitis occurs in critical ill patients with bad morbidity and mortality. It is known that imbalance of Th1 and Th2 lymphocytes differentiations plays a key role in its mechanisms. Recent studies indicated that type 1 membrane glycoprotein CD200 serves as co-inhibitory molecule, negatively regulating the immune response. In regard of this, we used Concanavalin A (Con A) induced liver injury model to research the effect of CD200 on the differentiation of CD4' T lymphocyte and found that the expression of CD200 on CD4(+) T was significantly higher in hepatitis mouse. The apoptosis of CD4(+) T cell in Con A induced liver injury was significantly attenuated by anti-CD200. The concentration of solube IL-2 and IFN-y was reduced by anti-CD200, in addition, the expression of T-bet, GATA3 and FoxP3 mRNA were all attenuated by anti-CD200. The phosphorylation of SH-2 containing inositol 5' polyphosphatase 1 (SHIP1) was significantly increased in Con A induced liver injury and reduced by anti-CD200. We hypothesized that, anti-CD200 inhibited the phosphorylation of SHIP1, the expression of T-bet, GATA3 and FoxP3 mRNA and CD4(+) T differentiation to protect the liver from autoimmune hepatitis.
更多查看译文
关键词
CD200,Hepatitis,CD4(+) T lymphocyte differentiation,mice
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要