Nanowire Based Guidance of the Morphology and Cytotoxic Activity of Natural Killer Cells

被引:16
作者
Bhingardive, Viraj [1 ,2 ]
Le Saux, Guillaume [1 ,2 ]
Edri, Avishay [3 ]
Porgador, Angel [3 ]
Schvartzman, Mark [1 ,2 ]
机构
[1] Ben Gurion Univ Negev, Dept Mat Engn, POB 653, IL-84105 Beer Sheva, Israel
[2] Ben Gurion Univ Negev, Ilse Katz Inst Nanoscale Sci & Technol, Shraga Segal Dept Microbiol, POB 653, IL-84105 Beer Sheva, Israel
[3] Ben Gurion Univ Negev, Genet Fac Hlth Sci, POB 653, IL-84105 Beer Sheva, Israel
基金
以色列科学基金会;
关键词
biofunctionalization; immunotherapy; natural killer cells; silicon nanowires; site selective functionalization; IMMUNOLOGICAL SYNAPSE; T-CELLS; ACTIVATION; RECEPTOR; GROWTH; COMMUNICATION; CD107A;
D O I
10.1002/smll.202007347
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The cytotoxic activity of natural killer (NK) cells is regulated by many chemical and physical cues, whose integration mechanism is still obscure. Here, a multifunctional platform is engineered for NK cell stimulation, to study the effect of the signal integration and spatial heterogeneity on NK cell function. The platform is based on nanowires, whose mechanical compliance and site-selective tip functionalization with antigens produce the physical and chemical stimuli, respectively. The nanowires are confined to micron-sized islands, which induce a splitting of the NK cells into two subpopulations with distinct morphologies and immune responses: NK cells atop the nanowire islands display symmetrical spreading and enhanced activation, whereas cells lying in the straits between the islands develop elongated profiles and show lower activation levels. The demonstrated tunability of NK cell cytotoxicity provides an important insight into the mechanism of their immune function and introduces a novel technological route for the ex vivo shaping of cytotoxic lymphocytes in immunotherapy.
引用
收藏
页数:12
相关论文
共 75 条
[21]   Receptor Signaling Clusters in the Immune Synapse [J].
Dustin, Michael L. ;
Groves, Jay T. .
ANNUAL REVIEW OF BIOPHYSICS, VOL 41, 2012, 41 :543-556
[22]   Human dendritic cells activate resting natural killer (NK) cells and are recognized via the NKp30 receptor by activated NK cells [J].
Ferlazzo, G ;
Tsang, ML ;
Moretta, L ;
Melioli, G ;
Steinman, RM ;
Münz, C .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (03) :343-351
[23]  
FUKUDA M, 1991, J BIOL CHEM, V266, P21327
[24]   The Immunological Synapse: A Molecular Machine Controlling T Cell Activation [J].
Grakoui, Arash ;
Bromley, Shannon K. ;
Sumen, Cenk ;
Davis, Mark M. ;
Shaw, Andrey S. ;
Allen, Paul M. ;
Dustin, Michael L. .
JOURNAL OF IMMUNOLOGY, 2015, 194 (09) :221-227
[25]   Growth and transport properties of complementary germanium nanowire field-effect transistors [J].
Greytak, AB ;
Lauhon, LJ ;
Gudiksen, MS ;
Lieber, CM .
APPLIED PHYSICS LETTERS, 2004, 84 (21) :4176-4178
[26]   Microchip screening Platform for single cell assessment of NK cell cytotoxicity [J].
Guldevall, Karolin ;
Brandt, Ludwig ;
Forslund, Elin ;
Olofsson, Karl ;
Frisk, Thomas W. ;
Olofsson, Per E. ;
Gustafsson, Karin ;
Manneberg, Otto ;
Vanherberghen, Bruno ;
Brismar, Hjalmar ;
Karre, Klas ;
Uhlin, Michael ;
Onfelt, Bjorn .
FRONTIERS IN IMMUNOLOGY, 2016, 7
[27]   Fifteen-Piconewton Force Detection from Neural Growth Cones Using Nanowire Arrays [J].
Hallstrom, Waldemar ;
Lexholm, Monica ;
Suyatin, Dmitry B. ;
Hammarin, Greger ;
Hessman, Dan ;
Samuelson, Lars ;
Montelius, Lars ;
Kanje, Martin ;
Prinz, Christelle N. .
NANO LETTERS, 2010, 10 (03) :782-787
[28]   Controversy and consensus regarding myosin II function at the immunological synapse [J].
Hammer, John A., III ;
Burkhardt, Janis K. .
CURRENT OPINION IN IMMUNOLOGY, 2013, 25 (03) :300-306
[29]   Characterization of the Cell-Nanopillar Interface by Transmission Electron Microscopy [J].
Hanson, Lindsey ;
Lin, Ziliang Carter ;
Xie, Chong ;
Cui, Yi ;
Cui, Bianxiao .
NANO LETTERS, 2012, 12 (11) :5815-5820
[30]   Crystallographic structure of an intact IgG1 monoclonal antibody [J].
Harris, LJ ;
Skaletsky, E ;
McPherson, A .
JOURNAL OF MOLECULAR BIOLOGY, 1998, 275 (05) :861-872