| Literature DB >> 30075430 |
Juyoung Kim1, Ji Sung Kim1, Hong Kyung Lee1, Hyung Sook Kim1, Eun Jae Park1, Jeong Eun Choi1, Yeo Jin Choi1, Bo Ram Shin1, Eun Young Kim1, Jin Tae Hong1, Youngsoo Kim1, Sang-Bae Han2.
Abstract
Natural killer (NK) cells eliminate cancer cells in a contact-dependent manner. However, how NK cells find cancer cells remain unclear. Here, using time-lapse imaging, we investigated how individual NK cells migrate toward cancer cells. Although naïve B16F10 cancer cells produce low levels of chemokines, IFN-γ-treated B16F10 cells secreted high levels of CXCL10, low levels of CCL5, but did not secrete CCL2, CCL7, or CXCL12. Wild-type NK cells migrated well toward cancer cells and killed them, whereas NK cells deficient in CXCR3 did not. CXCR3-deficient NK cells also showed slower migration speed than did wild-type NK cells. Taken together, our data show that NK cells find cancer cells, at least in part, by sensing CXCL10 produced by cancer cells and suggest that a strategy to increase CXCL10 secretion by cancer cells may improve the efficacy of NK cell-based immunotherapy.Entities:
Keywords: CXCL10–CXCR3 axis; Migration; Natural killer cells
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Year: 2018 PMID: 30075430 DOI: 10.1016/j.intimp.2018.07.026
Source DB: PubMed Journal: Int Immunopharmacol ISSN: 1567-5769 Impact factor: 4.932