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CD16A Shedding Regulates Innate Cell Engager‐Induced Serial Killing by Natural Killer Cells
1 Introduction Natural killer (NK) cells respond to malignantly transformed and virus-infected cells by direct cytotoxicity and release of pro-inflammatory cytokines. NK cells can be divided into two main subsets based on their expression of CD56 and the IgG receptor FcγRIIIA (CD16A). CD56bright CD16A− NK cells show strong cytokine production, while CD56dim CD16A+ NK cells instead show strong cytotoxic activity and represent approximately 90% of circulating NK cells in blood and spleen [1, 2].
Live single cell imaging assays in glass microwells produced by laser-induced deep etching
Live single cell imaging assays in glass microwells produced by laser-induced deep etching† Niklas Sandström, *a Ludwig Brandt, a Patrick A. Sandoz, a Chiara Zambarda,a Karolin Guldevall,a Malte Schulz-Ruhtenberg,b Bernd Rösener,b Robin A. Krügerb and Björn Önfelt *ac Abstract Miniaturization of cell culture substrates enables controlled analysis of living cells in confined micro-scale environments.
Author Correction: An optochemical tool for light-induced dissociation of adherens junctions to control mechanical coupling between cells
Correction to: Nature Communications https://doi.org/10.1038/s41467-020-14390-1, published online 24 January 2020 The original version of this Article contained an error in Fig. 7, in which panels s, t and u were described as being treated with Ha-pl-BG. They were treated with Ha-TMP. This has been corrected in both the PDF and HTML versions of the Article.
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