Journal
IMMUNITY
Volume 33, Issue 4, Pages 607-619Publisher
CELL PRESS
DOI: 10.1016/j.immuni.2010.09.009
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Funding
- Cancer Research Institute
- National Heart Lung and Blood Institute [K99HL102228]
- National Institutes of Health Building Interdisciplinary Research Careers in Women s Health (BIRCWH) center at UCLA [K12 HD001400]
- National Science Foundation
- National Cancer Institute [1K08CA133521]
- NIH [1R01A1079243 01]
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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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