多胺Putrescine是第3组天然淋巴细胞活化的正调节因子。

Prakash Sah, Lauren A Zenewicz
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引用次数: 1

摘要

第3组先天淋巴细胞(ILC3)对入侵的病原体或炎症信号快速反应,这需要改变细胞代谢需求。调节ILC3功能的代谢适应尚不完全清楚。多胺是聚阳离子代谢产物,在细胞功能和免疫调节免疫细胞生物学(包括Th17细胞)中具有不同的作用。多胺是否在ILC3活化中发挥作用尚不清楚。在这篇文章中,我们报道了多胺合成途径对ILC3的激活是重要的。IL-23激活的小鼠ILC3上调鸟氨酸脱羧酶,该酶催化多胺合成中鸟氨酸转化为腐胺的限速步骤,随后腐胺水平增加。通过特异性抑制剂α-二氟甲基鸟氨酸抑制鸟氨酸脱羧酶,以腐胺依赖的方式降低稳态或IL-23激活的ILC3产生的IL-22水平。因此,多胺腐胺是ILC3活化的正调节因子。我们的研究结果表明,在感染或炎症性疾病期间,多胺是治疗调节ILC3激活的潜在靶点。
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The Polyamine Putrescine Is a Positive Regulator of Group 3 Innate Lymphocyte Activation.

Group 3 innate lymphocytes (ILC3s) rapidly respond to invading pathogens or inflammatory signals, which requires shifting cellular metabolic demands. Metabolic adaptations regulating ILC3 function are not completely understood. Polyamines are polycationic metabolites that have diverse roles in cellular functions and in immunity regulate immune cell biology, including Th17 cells. Whether polyamines play a role in ILC3 activation is unknown. In this article, we report that the polyamine synthesis pathway is important for ILC3 activation. IL-23-activated mouse ILC3s upregulate ornithine decarboxylase, the enzyme catalyzing the rate-limiting step of the conversion of ornithine to putrescine in polyamine synthesis, with a subsequent increase in putrescine levels. Inhibition of ornithine decarboxylase via a specific inhibitor, α-difluoromethylornithine, reduced levels of IL-22 produced by steady-state or IL-23-activated ILC3s in a putrescine-dependent manner. Thus, the polyamine putrescine is a positive regulator of ILC3 activation. Our results suggest that polyamines represent a potential target for therapeutic modulation of ILC3 activation during infection or inflammatory disorders.

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