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Dedicator of Cytokinesis 8 Interacts with Talin and Wiskott-Aldrich Syndrome Protein To Regulate NK Cell Cytotoxicity
被引:91
作者:

Ham, Hyoungjun
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Mayo Clin, Coll Med, Dept Immunol, Rochester, MN 55905 USA Mayo Clin, Coll Med, Dept Immunol, Rochester, MN 55905 USA

Guerrier, Sabrice
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机构:
Carleton Coll, Dept Biol, Northfield, MN 55057 USA Mayo Clin, Coll Med, Dept Immunol, Rochester, MN 55905 USA

Kim, JungJin
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机构:
Carleton Coll, Coll Med, Div Oncol Res, Schulze Ctr Novel Therapeut, Northfield, MN 55057 USA Mayo Clin, Coll Med, Dept Immunol, Rochester, MN 55905 USA

Schoon, Renee A.
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Carleton Coll, Coll Med, Div Oncol Res, Schulze Ctr Novel Therapeut, Northfield, MN 55057 USA Mayo Clin, Coll Med, Dept Immunol, Rochester, MN 55905 USA

Anderson, Erik L.
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Mayo Clin, Coll Med, Dept Immunol, Rochester, MN 55905 USA
Bemidji State Univ, Biol Dept, Bemidji, MN 56601 USA Mayo Clin, Coll Med, Dept Immunol, Rochester, MN 55905 USA

Hamann, Michael J.
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Bemidji State Univ, Biol Dept, Bemidji, MN 56601 USA Mayo Clin, Coll Med, Dept Immunol, Rochester, MN 55905 USA

Lou, Zhenkun
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Carleton Coll, Coll Med, Div Oncol Res, Schulze Ctr Novel Therapeut, Northfield, MN 55057 USA Mayo Clin, Coll Med, Dept Immunol, Rochester, MN 55905 USA

Billadeau, Daniel D.
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h-index: 0
机构:
Mayo Clin, Coll Med, Dept Immunol, Rochester, MN 55905 USA
Carleton Coll, Coll Med, Div Oncol Res, Schulze Ctr Novel Therapeut, Northfield, MN 55057 USA Mayo Clin, Coll Med, Dept Immunol, Rochester, MN 55905 USA
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.
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页码:3661 / 3669
页数:9
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