期刊
JOURNAL OF IMMUNOLOGY
卷 197, 期 7, 页码 2909-2917出版社
AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1600651
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- NIAID NIH HHS [R01 AI095494, R01 AI059638, R01 AI101153] Funding Source: Medline
- NIGMS NIH HHS [R25 GM090084, K12 GM093857] Funding Source: Medline
Lactic acid (LA) is present in tumors, asthma, and wound healing, environments with elevated IL-33 and mast cell infiltration. Although IL-33 is a potent mast cell activator, how LA affects IL-33-mediated mast cell function is unknown. To investigate this, mouse bone marrow-derived mast cells were cultured with or without LA and activated with IL-33. LA reduced IL-33-mediated cytokine and chemokine production. Using inhibitors for monocarboxylate transporters (MCT) or replacing LA with sodium lactate revealed that LA effects are MCT-1- and pH-dependent. LA selectively altered IL-33 signaling, suppressing TGF-beta-activated kinase-1, JNK, ERK, and NF-kappa B phosphorylation, but not p38 phosphorylation. LA effects in other contexts have been linked to hypoxia-inducible factor (HIF)-1 alpha, which was enhanced in bone marrow-derived mast cells treated with LA. Because HIF-1 alpha has been shown to regulate the microRNA miR-155 in other systems, LA effects on miR-155-5p and miR-155-3p species were measured. In fact, LA selectively suppressed miR-155-5p in an HIF-1 alpha-dependent manner. Moreover, overexpressing miR-155-5p, but not miR-155-3p, abolished LA effects on IL-33-induced cytokine production. These in vitro effects of reducing cytokines were consistent in vivo, because LA injected i.p. into C57BL/6 mice suppressed IL-33-induced plasma cytokine levels. Lastly, IL-33 effects on primary human mast cells were suppressed by LA in an MCT-dependent manner. Our data demonstrate that LA, present in inflammatory and malignant microenvironments, can alter mast cell behavior to suppress inflammation.
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