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Rhomboid domain-containing protein 3 is a negative regulator of TLR3-triggered natural killer cell activation
Juan Liu, Shuxun Liu, Meng Xia, Sheng Xu, Chunmei Wang, Yan Bao, Minghong Jiang, Yue Wu, Tian Xu and Xuetao Cao
Proceedings of the National Academy of Sciences of the United States of America
Vol. 110, No. 19 (May 7, 2013), pp. 7814-7819
Published by: National Academy of Sciences
Stable URL: http://www.jstor.org/stable/42656388
Page Count: 6
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Rhomboid domain-containing protein 3 (Rhbdd3), which belongs to a family of proteins with rhomboid domain, is widely expressed in immune cells; however, the roles of the Rhbdd members, including Rhbdd3, in immunity remain unknown. Natural killer (NK) cells are critical for host immune defense and also can mediate inflammatory diseases such as hepatitis. Although much is known about how NK cells are activated, the detailed mechanisms for negative regulation of NK cell activation remain to be fully understood. Using Rhbdd3-deficient mice, we reveal that Rhbdd3, selectively up-regulated in NK cells upon Toll-like receptor 3 (TLR3) stimulation, negatively regulates TLR3-mediated NK cell activation in a feedback manner. Rhbdd3 inhibits TLR3-triggered IFN-γ and granzyme B expression of NK cells in cell-cell contact dependence of accessory cells such as dendritic cells and Kupffer cells. Rhbdd3 interacts with DNAX activation protein of 12 kDa and promotes its degradation, inhibiting MAPK activation in TLR3-triggered NK cells. Furthermore, Rhbdd3 plays a critical role in attenuating TLR3-triggered acute inflammation by controlling NK cell activation and accumulation in liver and disrupting NK cell-Kupffer cell interaction. Therefore, Rhbdd3 is a feedback inhibitor of TLR3-triggered NK cell activation. Our study outlines a mechanism for the negative regulation of NK cell activation and also provides clues for the function of the rhomboid proteins in immunity.
Proceedings of the National Academy of Sciences of the United States of America © 2013 National Academy of Sciences