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Myosin IIA Associates with NK Cell Lytic Granules to Enable Their Interaction with F-Actin and Function at the Immunological Synapse
Abstract
NK cell cytotoxicity requires the formation of an actin-rich immunological synapse (IS) with a target cell and the polarization of perforin-containing lytic granules toward the IS. Following the polarization of lytic granules, they traverse through the actin-rich IS to join the NK cell membrane in order for directed secretion of their contents to occur. We examined the role of myosin IIA as a candidate for facilitating this prefinal step in lytic NK cell IS function. Lytic granules in and derived from a human NK cell line, or ex vivo human NK cells, were constitutively associated with myosin IIA. When isolated using density gradients, myosin IIA-associated NK cell lytic granules directly bound to F-actin and the interaction was sensitive to the presence of ATP under conditions of flow. In NK cells from patients with a truncation mutation in myosin IIA, NK cell cytotoxicity, lytic granule penetration into F-actin at the IS, and interaction of isolated granules with F-actin were all decreased. Similarly, inhibition of myosin function also diminished the penetration of lytic granules into F-actin at the IS, as well as the final approach of lytic granules to and their dynamics at the IS. Thus, NK cell lytic granule-associated myosin IIA enables their interaction with actin and final transit through the actin-rich IS to the synaptic membrane, and can be defective in the context of naturally occurring human myosin IIA mutation.
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“Therefore, our data confirm the previously reported function of myosin IIA in terms of translocation of granules and mitochondria in other cell types such as NK cells and thrombocytes [46–49].”
From Nascent RHOH acts as a molecular brake on actomyosin-mediated effector functions of inflammatory neutrophils (2022) · cites this paper as [47]
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Cites
Functions of natural killer cells
Vivier, E., Tomasello, E., Baratin, M., Walzer, T., & Ugolini, S. (2008) · Nature Immunology · doi:10.1038/ni1582 · Cited by 3,943
Research works printed but not linked: 60
- 2004, What is the importance of the immunological synapse?., 323
- 2008, Formation and function of the lytic NK-cell immunological synapse., 713
- 2006, Centrosome polarization delivers secretory granules to the immunological synapse., 462
- 1991, Cytotoxic T lymphocyte granules are secretory lysosomes, containing both perforin and granzymes., 1099
- 2007, Cdc42-interacting protein-4 functionally links actin and microtubule networks at the cytolytic NK cell immunological synapse., 2305
- 2003, The mature activating natural killer cell immunologic synapse is formed in distinct stages., 14151
- 1991, Polarized expression of cytokines in cell conjugates of helper T cells and splenic B cells., 775
- 2006, CD28-stimulated ERK2 phosphorylation is required for polarization of the microtubule organizing center and granules in YTS NK cells., 10346
- 2005, Human decidual NK cells form immature activating synapses and are not cytotoxic., 15563
- 2003, Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3)., 461
- 2007, Secretory cytotoxic granule maturation and exocytosis require the effector protein hMunc13-4., 257
- 2000, Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome., 173
- 2007, Defective cytotoxic lymphocyte degranulation in syntaxin-11 deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients., 1906
- 2004, A single class II myosin modulates T cell motility and stopping, but not synapse formation., 531
- 2007, Myosin IIA is required for cytolytic granule exocytosis in human NK cells., 2285
- 2006, Phosphorylation of nonmuscle myosin heavy chain IIA on Ser1917 is mediated by protein kinase CβII and coincides with the onset of stimulated degranulation of RBL-2H3 mast cells., 1492
- 2004, Dictyostelium PAKc is required for proper chemotaxis., 5456
- 2002, Myosin VI is required for E-cadherin-mediated border cell migration., 616
- 1999, A targeted gene silencing technique shows that Drosophila myosin VI is required for egg chamber and imaginal disc morphogenesis., 3677
- 2006, Formation of a WIP-, WASp-, actin-, and myosin IIA-containing multiprotein complex in activated NK cells and its alteration by KIR inhibitory signaling., 121
- 2000, Myosins: a diverse superfamily., 3
- 2007, Myosin II isoforms in smooth muscle: heterogeneity and function., C493
- 2001, The tip of the coiled-coil rod determines the filament formation of smooth muscle and nonmuscle myosin., 30293
- 1983, The proteolytic substructure of light meromyosin: localization of a region responsible for the low ionic strength insolubility of myosin., 13213
- 1986, Solubility-determining domain of smooth muscle myosin rod., 355
- 1990, Identification of functional regions on the tail of Acanthamoeba myosin-II using recombinant fusion proteins, II: assembly properties of tails with NH2- and COOH-terminal deletions., 2417
- 2003, Dissecting temporal and spatial control of cytokinesis with a myosin II Inhibitor., 1743
- 1987, Selective inhibition of catalytic activity of smooth muscle myosin light chain kinase., 7796
- 2000, Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes: the May-Heggllin/Fechtner Syndrome Consortium., 103
- 2003, MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness., 203
- 2000, Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly., 106
- 2001, Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes., 1033
- 2002, Wiskott-Aldrich syndrome protein is required for NK cell cytotoxicity and colocalizes with actin to NK cell-activating immunologic synapses., 11351
- 2008, IFN-γ production and degranulation are differentially regulated in response to stimulation in murine natural killer cells., 1
- 1985, Sliding distance of actin filament induced by a myosin crossbridge during one ATP hydrolysis cycle., 366
- 2004, Phototoxicity and photoinactivation of blebbistatin in UV and visible light., 1020
- 1990, The lytic granules of natural killer cells are dual-function organelles combining secretory and pre-lysosomal compartments., 2327
- 2001, The immunological synapse of CTL contains a secretory domain and membrane bridges., 751
- 2001, Spatial organization of signal transduction molecules in the NK cell immune synapses during MHC class I-regulated noncytolytic and cytolytic interactions., 4358
- 2002, Myosin-V, a versatile motor for short-range vesicle transport., 859
- 1999, Vesicle transport: the role of actin filaments and myosin motors., 93
- 1999, Specific isoforms of actin-binding proteins on distinct populations of Golgi-derived vesicles., 10743
- 1997, Myosin II is associated with Golgi membranes: identification of p200 as nonmuscle myosin II on Golgi-derived vesicles., 2155
- 2007, Membrane associated nonmuscle myosin II functions as a motor for actin-based vesicle transport in clam oocyte extracts., 739
- 2008, Myosin II contributes to fusion pore expansion during exocytosis., 10949
- 2004, New roles of myosin II during vesicle transport and fusion in chromaffin cells., 27450
- 2002, Protein phosphatases 1 and 2A transiently associate with myosin during the peak rate of secretion from mast cells., 1083
- 1994, Direct binding of myosin II to phospholipid vesicles via tail regions and phosphorylation of the heavy chains by protein kinase C., 16082
- 1994, Association of a cellular myosin II with anionic phospholipids and the neuronal plasma membrane., 853
- 2006, In vitro reconstitution of a transport complex containing Rab27a, melanophilin and myosin Va., 5863
- 2008, WIP is essential for lytic granule polarization and NK cell cytotoxicity., 2568
- 2007, Organelle proteomics: identification of the exocytic machinery associated with the natural killer cell secretory lysosome., 767
- 2001, Functional dichotomy in natural killer cell signaling: Vav1-dependent and -independent mechanisms., 1413
- 2005, Relative contributions of NK and CD8 T cells to IFN-γ mediated innate immune protection against Listeria monocytogenes., 1751
- 2005, Rod mutations associated with MYH9-related disorders disrupt nonmuscle myosin-IIA assembly., 161
- 2004, Relating biochemistry and function in the myosin superfamily., 61
- 1998, Two nonmuscle myosin II heavy chain isoforms expressed in rabbit brains: filament forming properties, the effects of phosphorylation by protein kinase C and casein kinase II, and location of the phosphorylation sites., 1989
- 1991, Identification of the serine residue phosphorylated by protein kinase C in vertebrate nonmuscle myosin heavy chains., 966
- 1993, Phosphorylation of vertebrate nonmuscle and smooth muscle myosin heavy chains and light chains., 219
- 1998, Metastasis-associated Mts1 (S100A4) protein modulates protein kinase C phosphorylation of the heavy chain of nonmuscle myosin., 9852
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Cook, S. A., Comrie, W. A., Poli, M. C., Similuk, M., Oler, A. J., Faruqi, A. J., Kuhns, D. B., Yang, S., Vargas-Hernández, A., Carisey, A. F., et al. (2020) · Science · doi:10.1126/science.aay5663 · Cited by 102
Self-citationSubstance P inhibits natural killer cell cytotoxicity through the neurokinin-1 receptor
Monaco-Shawver, L., Schwartz, L., Tuluc, F., Guo, C.-J., Lai, J. P., Gunnam, S. M., Kilpatrick, L. E., Banerjee, P. P., Douglas, S. D., & Orange, J. S. (2010) · Journal of Leukocyte Biology · doi:10.1189/jlb.0410200 · Cited by 39
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Metadata
- Authors
- Sanborn, K. B., Rak, G. D., Maru, S. Y., Demers, K., Difeo, A., Martignetti, J. A., Betts, M. R., Favier, R., Banerjee, P. P., & Orange, J. S.
- Affiliations
- Immunology Graduate Group, University of Pennsylvania School of Medicine , Philadelphia, PA 19104
- Cell Biology and Physiology Graduate Program, University of Pennsylvania School of Medicine , Philadelphia, PA 19104
- Joseph Stokes Jr. Research Institute of the Children’s Hospital of Philadelphia , Philadelphia, PA 19104
- Department of Microbiology, University of Pennsylvania , Philadelphia, PA 19104
- Department of Genetics and Genomic Sciences, Mount Sinai School of Medicine , New York, NY 10029
- Assistance Publique-Hôpitaux de Paris, Centre de Référence des Pathologies Plaquettaires, Armand Trousseau Children’s Hospital , 75012; INSERM U790, Villejuif,
- Venue
- The Journal of Immunology
- Publisher
- Oxford University Press (OUP)
- Published
- 2009-06-01
- Volume
- 182
- Issue
- 11
- Pages
- 6969-6984
- ISSN
- 1550-6606
- 0022-1767
- PMC
- PMC2835774
- Cited by
- 87
- References
- 1
- Language
- en
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