Dedicator of Cytokinesis 8 Interacts with Talin and Wiskott-Aldrich Syndrome Protein To Regulate NK Cell Cytotoxicity

被引:91
作者
Ham, Hyoungjun [1 ]
Guerrier, Sabrice [2 ]
Kim, JungJin [3 ]
Schoon, Renee A. [3 ]
Anderson, Erik L. [1 ,4 ]
Hamann, Michael J. [4 ]
Lou, Zhenkun [3 ]
Billadeau, Daniel D. [1 ,3 ]
机构
[1] Mayo Clin, Coll Med, Dept Immunol, Rochester, MN 55905 USA
[2] Carleton Coll, Dept Biol, Northfield, MN 55057 USA
[3] Carleton Coll, Coll Med, Div Oncol Res, Schulze Ctr Novel Therapeut, Northfield, MN 55057 USA
[4] Bemidji State Univ, Biol Dept, Bemidji, MN 56601 USA
关键词
NATURAL-KILLER-CELLS; IMMUNOLOGICAL SYNAPSE; INTEGRIN ACTIVATION; MEDIATED CYTOTOXICITY; DOCK8; DEFICIENCY; ARP2/3; COMPLEX; POLARIZATION; ACTIN; CDC42; WASP;
D O I
10.4049/jimmunol.1202792
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recently, patients with mutations in DOCK8 have been reported to have a combined immunodeficiency characterized by cutaneous viral infections and allergies. NK cells represent a first-line defense against viral infections, suggesting that DOCK8 might participate in NK cell function. In this study, we demonstrate that DOCK8-suppressed human NK cells showed defects in natural cytotoxicity as well as specific activating receptor-mediated NK cytotoxicity. Additionally, compared with control NK cells, NK cells depleted of DOCK8 showed defective conjugate formation, along with decreased polarization of LFA-1, F-actin, and cytolytic granules toward the cytotoxic synapse. Using a proteomic approach, we found that DOCK8 exists in a macromolecular complex with the Wiskott-Aldrich syndrome protein, an actin nucleation-promoting factor activated by CDC42, as well as talin, which is required for integrin-mediated adhesion. Taken together, our results demonstrate an important role for DOCK8 in NK cell effector function and provide important new mechanistic insight into how DOCK8 regulates F-actin and integrin-mediated adhesion in immune cells. The Journal of Immunology, 2013, 190: 3661-3669.
引用
收藏
页码:3661 / 3669
页数:9
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