共 43 条
MicroRNA-155 Promotes Autoimmune Inflammation by Enhancing Inflammatory T Cell Development
被引:842
作者:
O'Connell, Ryan M.
[1
]
Kahn, Daniel
[1
,2
]
Gibson, William S. J.
[1
]
Round, June L.
[1
]
Scholz, Rebecca L.
[1
]
Chaudhuri, Aadel A.
[1
]
Kahn, Melissa E.
[4
]
Rao, Dinesh S.
[1
,3
]
Baltimore, David
[1
]
机构:
[1] CALTECH, Div Biol, Pasadena, CA 91125 USA
[2] Univ Calif Los Angeles, Div Maternal Fetal Med, Dept Obstet & Gynecol, David Geffen Sch Med, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Pathol & Lab Med, David Geffen Sch Med, Los Angeles, CA 90095 USA
[4] Cedars Sinai Med Ctr, Dept Pathol & Lab Med, Los Angeles, CA 90048 USA
来源:
基金:
美国国家卫生研究院;
美国国家科学基金会;
关键词:
CUTTING EDGE;
TGF-BETA;
DIFFERENTIATION;
ACTIVATION;
EXPRESSION;
TARGET;
ROLES;
MICE;
GENERATION;
PATHWAY;
D O I:
10.1016/j.immuni.2010.09.009
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Mammalian noncoding microRNAs (miRNAs) are a class of gene regulators that have been linked to immune system function Here, we have investigated the role of miR-155 during an autoimmune inflammatory disease Consistent with a positive role for mir155(-/-) in mediating inflammatory responses, Mir155(-/-) mice were highly resistant to experimental autoimmune encephalomyelitis (EAE) miR-155 functions in the hematopoietic compartment to promote the development of inflammatory T cells including the T helper 17 (Th17) cell and Th1 cell subsets Furthermore, the major contribution of miR-155 to EAE was CD4(+) T cell intrinsic, whereas miR-155 was also required for optimum dendritic cell production of cytokines that promoted Th17 cell formation Our study shows that one aspect of miR-155 function is the promotion of T cell-dependent tissue inflammation, suggesting that miR-155 might be a promising therapeutic target for the treatment of autoimmune disorders
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页码:607 / 619
页数:13
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