Cutting Edge: Down-Regulation of MHC Class I-Related Chain A on Tumor Cells by IFN-γ-Induced MicroRNA

被引:89
作者
Yadav, Deepak [1 ]
Ngolab, Jennifer [1 ]
Lim, Rod Seung-Hwan [1 ]
Krishnamurthy, Siddharth [1 ]
Bui, Jack D. [1 ]
机构
[1] Univ Calif San Diego, Dept Pathol, La Jolla, CA 92093 USA
关键词
INTERFERON-GAMMA; RECEPTOR NKG2D; NK CELLS; EXPRESSION; LIGANDS; ACTIVATION; SUPPRESSION; MECHANISM; PROTEIN;
D O I
10.4049/jimmunol.182.1.39
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:39 / 43
页数:5
相关论文
共 23 条
  • [1] MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004)
    Bartel, David P.
    [J]. CELL, 2007, 131 (04) : 11 - 29
  • [2] Activation of NK Cells and T Cells by NKG2D, a Receptor for Stress-Inducible MICA
    Bauer, Stefan
    Groh, Veronika
    Wu, Jun
    Steinle, Alexander
    Phillips, Joseph H.
    Lanier, Lewis L.
    Spies, Thomas
    [J]. JOURNAL OF IMMUNOLOGY, 2018, 200 (07) : 2231 - 2233
  • [3] Principles of MicroRNA-target recognition
    Brennecke, J
    Stark, A
    Russell, RB
    Cohen, SM
    [J]. PLOS BIOLOGY, 2005, 3 (03): : 404 - 418
  • [4] IFN-Dependent down-regulation of the NKG2D ligand H60 on tumors
    Bui, JD
    Carayannopoulos, LN
    Lanier, LL
    Yokoyama, WM
    Schreiber, RD
    [J]. JOURNAL OF IMMUNOLOGY, 2006, 176 (02) : 905 - 913
  • [5] Ligands for natural killer cell receptors: redundancy or specificity
    Cerwenka, A
    Lanier, LL
    [J]. IMMUNOLOGICAL REVIEWS, 2001, 181 : 158 - 169
  • [6] Ligands for the murine NKG2D receptor: expression by tumor cells and activation of NK cells and macrophages
    Diefenbach, A
    Jamieson, AM
    Liu, SD
    Shastri, N
    Raulet, DH
    [J]. NATURE IMMUNOLOGY, 2000, 1 (02) : 119 - 126
  • [7] Interferons, immunity and cancer immunoediting
    Dunn, Gavin P.
    Koebel, Catherine M.
    Schreiber, Robert D.
    [J]. NATURE REVIEWS IMMUNOLOGY, 2006, 6 (11) : 836 - 848
  • [8] Tumour-derived soluble MIC ligands impair expression of NKG2D and T-cell activation
    Groh, V
    Wu, J
    Yee, C
    Spies, T
    [J]. NATURE, 2002, 419 (6908) : 734 - 738
  • [9] Cell stress-regulated human major histocompatibility complex class I gene expressed in gastrointestinal epithelium
    Groh, V
    Bahram, S
    Bauer, S
    Herman, A
    Beauchamp, M
    Spies, T
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (22) : 12445 - 12450
  • [10] A novel role of Sp1 and Sp3 in the interferon-γ-mediated suppression of macrophage lipoprotein lipase gene transcription
    Hughes, TR
    Tengku-Muhammad, TS
    Irvine, SA
    Ramji, DP
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (13) : 11097 - 11106