Tumor-associated macrophages are shaped by intratumoral high potassium via Kir2.1
Cell Metabolism(2022)
Abstract
The tumor microenvironment (TME) is a unique niche governed by constant crosstalk within and across all intratumoral cellular compartments. In particular, intratumoral high potassium (K+) has shown immune -sup-pressive potency on T cells. However, as a pan-cancer characteristic associated with local necrosis, the impact of this ionic disturbance on innate immunity is unknown. Here, we reveal that intratumoral high K+ suppresses the anti-tumor capacity of tumor-associated macrophages (TAMs). We identify the inwardly rectifying K+ channel Kir2.1 as a central modulator of TAM functional polarization in high K+ TME, and its conditional depletion repolarizes TAMs toward an anti-tumor state, sequentially boosting local anti-tumor immunity. Kir2.1 deficiency disturbs the electrochemically dependent glutamine uptake, engendering TAM metabolic reprogramming from oxidative phosphorylation toward glycolysis. Kir2.1 blockade attenuates both murine tumor-and patient-derived xenograft growth. Collectively, our findings reveal Kir2.1 as a deter-minant and potential therapeutic target for regaining the anti-tumor capacity of TAMs within ionic-imbal-anced TME.
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Key words
tumor microenvironment,tumor-associated macrophage,Kir2.1,immunometabolism,potassium
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