| Literature DB >> 35113018 |
Hiroshi Ichise1, Shoko Tsukamoto1, Tsuyoshi Hirashima2, Yoshinobu Konishi1, Choji Oki3, Shinya Tsukiji3, Satoshi Iwano4, Atsushi Miyawaki4, Kenta Sumiyama5, Kenta Terai1, Michiyuki Matsuda1,2,6.
Abstract
Natural killer (NK) cells lyse invading tumor cells to limit metastatic growth in the lung, but how some cancers evade this host protective mechanism to establish a growing lesion is unknown. Here, we have combined ultra-sensitive bioluminescence imaging with intravital two-photon microscopy involving genetically encoded biosensors to examine this question. NK cells eliminated disseminated tumor cells from the lung within 24 hr of arrival, but not thereafter. Intravital dynamic imaging revealed that 50% of NK-tumor cell encounters lead to tumor cell death in the first 4 hr after tumor cell arrival, but after 24 hr of arrival, nearly 100% of the interactions result in the survival of the tumor cell. During this 24-hr period, the probability of ERK activation in NK cells upon encountering the tumor cells was decreased from 68% to 8%, which correlated with the loss of the activating ligand CD155/PVR/Necl5 from the tumor cell surface. Thus, by quantitatively visualizing, the NK-tumor cell interaction at the early stage of metastasis, we have revealed the crucial parameters of NK cell immune surveillance in the lung.Entities:
Keywords: cell biology; circulating tumor cell; immunology; inflammation; intravital imaging; lung metastasis; mouse; natural killer cells; tumor immunology
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Year: 2022 PMID: 35113018 PMCID: PMC8849286 DOI: 10.7554/eLife.76269
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140