Dynamin 2 Regulates Granule Exocytosis during NK Cell-Mediated Cytotoxicity
Author(s) -
Laura N. Arneson,
Colin M. Segovis,
Timothy S. Gomez,
Renee A. Schoon,
Christopher J. Dick,
Zhenkun Lou,
Daniel D. Billadeau,
Paul J. Leibson
Publication year - 2008
Publication title -
the journal of immunology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.181.10.6995
Subject(s) - dynamin , microbiology and biotechnology , exocytosis , lytic cycle , cytotoxicity , granule (geology) , secretion , biology , cell , gtpase , endosome , innate immune system , endocytosis , immune system , immunology , in vitro , biochemistry , virus , paleontology , intracellular
NK cells are innate immune cells that can eliminate their targets through granule release. In this study, we describe a specialized role for the large GTPase Dynamin 2 (Dyn2) in the regulation of these secretory events leading to cell-mediated cytotoxicity. By modulating the expression of Dyn2 using small interfering RNA or by inhibiting its activity using a pharmacological agent, we determined that Dyn2 does not regulate conjugate formation, proximal signaling, or granule polarization. In contrast, during cell-mediated killing, Dyn2 localizes with lytic granules and polarizes to the NK cell-target interface where it regulates the final fusion of lytic granules with the plasma membrane. These findings identify a novel role for Dyn2 in the exocytic events required for effective NK cell-mediated cytotoxicity.
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