期刊
JOURNAL OF IMMUNOLOGY
卷 182, 期 1, 页码 39-43出版社
AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.182.1.39
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资金
- American Cancer Society [70-002]
- Cancer Research Coordinating Committee [6-444951-34384]
- V Foundation Scholar Award
- NATIONAL CANCER INSTITUTE [K08CA128893] Funding Source: NIH RePORTER
NKG2D is a receptor used by NK cells to detect virally infected and transformed cells. It recognizes ligands that are expressed constitutively on primary tumors and tumor cell lines. In this report, we have identified four microRNAs (miRNAs) that each was sufficient to reduce the expression of the NKG2D ligand MHC class I-related chain A (MICA). One of these miRNAs (miR-520b) was induced by IFN-gamma, leading to a reduction in MICA surface protein levels. Interestingly, miR-520b acted on both the MICA 3'-untranslated region and the promoter region and caused a decrease in the levels of MICA transcript. In contrast, an antisense oligonucleotide inhibitor of miR-520b increased the expression of a reporter construct containing the MICA 3'-untranslated region but not the MICA promoter region. These findings demonstrate the novel regulation of an NKG2D ligand by an endogenous microRNA that is itself induced by IFN-gamma. The Journal of Immunology, 2009, 182: 39-43.
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