VAMP4‐ and VAMP7‐expressing vesicles are both required for cytotoxic granule exocytosis in NK cells

NK cells eliminate cancer and virus‐infected cells through their cytolytic activity. The last step in NK‐cell cytotoxicity, resulting in exocytosis of granule content, requires fusion of lytic granules with the plasma membrane. Proteins from the soluble N‐ethylmaleimide‐sensitive factor attachment protein receptor (SNARE) family mediate membrane fusion events in the cell. Here, we show that NK cells express all members of the R‐SNARE subgroup. Two of these R‐SNARE proteins, VAMP4 and VAMP7, colocalize with lytic granules during cytotoxic interactions. However, only VAMP7 associates with perforin‐containing granules in nonactivated cells, indicating that the two VAMPs have different functions in exocytosis. Using both the tumor NK‐cell line YTS and the peripheral NK cells, we show that the disruption of expression of either VAMP4 or VAMP7 inhibits the release of lytic granules and severely impairs NK‐cell cytotoxic activity. Furthermore, VAMP7 but not VAMP4 is involved in IFN‐γ secretion in NK cells, indicating that VAMP7 is involved in many fusion processes and thus plays a more general function in NK‐cell activity than VAMP4.

[1]  W. Hong,et al.  A role for endobrevin/VAMP8 in CTL lytic granule exocytosis , 2009, European journal of immunology.

[2]  T. Südhof,et al.  Membrane Fusion: Grappling with SNARE and SM Proteins , 2009, Science.

[3]  A. Tanimura,et al.  Role of VAMP8/endobrevin in constitutive exocytotic pathway in HeLa cells. , 2009, Cell structure and function.

[4]  J. Strominger,et al.  The killer's kiss: the many functions of NK cell immunological synapses. , 2008, Current opinion in cell biology.

[5]  J. Meldolesi,et al.  The regulated exocytosis of enlargeosomes is mediated by a SNARE machinery that includes VAMP4 , 2008, Journal of Cell Science.

[6]  J. Orange Formation and function of the lytic NK-cell immunological synapse , 2008, Nature Reviews Immunology.

[7]  Eric O Long,et al.  Line of attack: NK cell specificity and integration of signals. , 2008, Current opinion in immunology.

[8]  Lewis L Lanier,et al.  Up on the tightrope: natural killer cell activation and inhibition , 2008, Nature Immunology.

[9]  Eric Vivier,et al.  Functions of natural killer cells , 2008, Nature Immunology.

[10]  T. Galli,et al.  Vesicle associated membrane protein (VAMP)‐7 and VAMP‐8, but not VAMP‐2 or VAMP‐3, are required for activation‐induced degranulation of mature human mast cells , 2008, European journal of immunology.

[11]  X. Chen,et al.  WIP is essential for lytic granule polarization and NK cell cytotoxicity , 2008, Proceedings of the National Academy of Sciences.

[12]  Paige Lacy,et al.  Vesicle-associated membrane protein 7 (VAMP-7) is essential for target cell killing in a natural killer cell line. , 2008, Biochemical and biophysical research communications.

[13]  J. Stow,et al.  SNAREing immunity: the role of SNAREs in the immune system , 2006, Nature Reviews Immunology.

[14]  Reinhard Jahn,et al.  SNAREs — engines for membrane fusion , 2006, Nature Reviews Molecular Cell Biology.

[15]  H. Kita,et al.  A critical role for vesicle‐associated membrane protein‐7 in exocytosis from human eosinophils and neutrophils , 2006, Allergy.

[16]  H. Sugiya,et al.  Difference in distribution of membrane proteins between low- and high-density secretory granules in parotid acinar cells. , 2006, Biochemical and biophysical research communications.

[17]  Varpu Marjomäki,et al.  BioImageXD - New Open Source Free Software for the Processing, Analysis and Visualization of Multidimensional Microscopic Images , 2006, Microscopy Today.

[18]  J. Orange,et al.  Natural killer cells in human health and disease. , 2006, Clinical immunology.

[19]  T. Galli,et al.  [Activation-induced polarized recycling targets T cell receptors to the immunological synapse]. , 2005, Medecine sciences : M/S.

[20]  J. Sibarita,et al.  TI‐VAMP/VAMP7 is required for optimal phagocytosis of opsonised particles in macrophages , 2004, The EMBO journal.

[21]  B. Nal,et al.  Activation-induced polarized recycling targets T cell antigen receptors to the immunological synapse; involvement of SNARE complexes. , 2004, Immunity.

[22]  Jung Hun Song,et al.  Thyrotropin-Mediated Repression of Class II Trans-Activator Expression in Thyroid Cells: Involvement of STAT3 and Suppressor of Cytokine Signaling1 , 2003, The Journal of Immunology.

[23]  G. Griffiths,et al.  The immunological synapse of CTL contains a secretory domain and membrane bridges. , 2001, Immunity.

[24]  B. Eaton,et al.  Biogenesis of Regulated Exocytotic Carriers in Neuroendocrine Cells , 2000, The Journal of Neuroscience.

[25]  O. Mandelboim,et al.  The human natural killer cell immune synapse. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[26]  R. Scheller,et al.  Vesicle-associated membrane protein 4 is implicated in trans-Golgi network vesicle trafficking. , 1999, Molecular biology of the cell.

[27]  Colin R. F. Monks,et al.  Three-dimensional segregation of supramolecular activation clusters in T cells , 1998, Nature.

[28]  G J Brakenhoff,et al.  Dynamics of three-dimensional replication patterns during the S-phase, analysed by double labelling of DNA and confocal microscopy. , 1992, Journal of cell science.