iScienceImmunologyPeer-reviewed journal article
Hepatic iNKT cells facilitate colorectal cancer metastasis by inducing a fibrotic niche in the liver
Marc NateriD, Michael David BrüggeriD, Virginia Cecconi, Paulo Pereira, Geo Forni, Hakan KöksaliD, Despoina Dimakou, Michael HerbstiD, Anna Laura Calvanese, Giulia Lucchiari, Christoph SchneideriD, Tomáš ValentaiD, Maries F. van den BroekiD
Abstract
The liver is an important metastatic organ that contains many innate immune cells, yet little is known about their role in anti-metastatic defense. We investigated how invariant natural killer T (iNKT) cells influence colorectal cancer-derived liver metastasis using different models in immunocompetent mice. We found that hepatic iNKT cells promote metastasis by creating a supportive niche for disseminated cancer cells. Mechanistically, iNKT cells respond to disseminating cancer cells by producing the fibrogenic cytokines IL-4 and IL-13 in a TCR-independent manner. Selective abrogation of IL-4 and IL-13 sensing in hepatic stellate cells prevented their transdifferentiation into extracellular matrix-producing myofibroblasts, which hindered metastatic outgrowth of disseminated cancer cells. This study highlights a novel tumor-promoting axis driven by iNKT cells in the initial stages of metastasis.
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