Enhanced Calcium Signal Induces NK Cell Degranulation but Inhibits Its Cytotoxic Activity
Author(s) -
Yang Li,
Minghang Yu,
Jie Yin,
Han Yan,
Xi Wang
Publication year - 2021
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.2001141
Subject(s) - degranulation , cytotoxic t cell , microbiology and biotechnology , lytic cycle , immunological synapse , exocytosis , cytotoxicity , calcium , secretion , cytolysis , calcium signaling , chemistry , biology , signal transduction , immunology , biochemistry , t cell , in vitro , immune system , virus , receptor , t cell receptor , organic chemistry
Although the mechanism of NK cell activation is still unclear, the strict calcium dependence remains the hallmark for lytic granule secretion. A plethora of studies claiming that impaired Ca 2+ signaling leads to severely defective cytotoxic granule exocytosis accompanied by weak target cell lysis has been published. However, there has been little discussion about the effect of induced calcium signal on NK cell cytotoxicity. In our study, we observed that small-molecule inhibitor UNC1999, which suppresses global H3K27 trimethylation (H3K27me3) of human NK cells, induced a PKD2-dependent calcium signal. Enhanced calcium entry led to unbalanced vesicle release, which resulted into fewer target cells acquiring lytic granules and subsequently being killed. Further analyses revealed that the ability of conjugate formation, lytic synapse formation, and granule polarization were normal in NK cells treated with UNC1999. Cumulatively, these data indicated that induced calcium signal exclusively enhances unbalanced degranulation that further inhibits their cytotoxic activity in human NK cells.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom