Department of Pathology and Molecular Medicine, McMaster Immunology Research Centre, McMaster University, Hamilton, ON, Canada.
Front Immunol. 2019 Jun 19;10:1414. doi: 10.3389/fimmu.2019.01414. eCollection 2019.
NK cells are capable of an array of functions that range widely from their classic anti-tumor and anti-viral cytotoxic effector functions, to their critical regulatory roles in controlling inflammatory immune responses and promoting tissue growth. However, the mechanisms that polarize NK cells to these distinct and opposing functions are incompletely understood. NK cell functional subsets are primarily identified and studied based on phenotype, which has served as an accessible means for profiling NK cells and does offer information on NK cell activation state. However, inconsistencies have emerged in using classic phenotypes to inform function, which raise the questions: Can phenotype in fact define NK cell functional fate? What factors do profile and drive NK cell fate? In other immune cells, cell metabolism has been shown to critically determine subset polarization. There is a growing body of evidence that cell metabolism is integral to NK cell effector functions. Glucose-driven glycolysis and oxidative metabolism have been shown to drive classic NK cell anti-tumor and anti-viral effector functions. Recent studies have uncovered a critical role for metabolism in NK cell development, education, and memory generation. In this review, we will draw on the evidence to date to investigate the relationship between NK cell phenotype, metabolism, and functional fate. We explore a paradigm in which the differential activity of metabolic pathways within NK cells produce distinct metabolic fingerprints that comprehensively distinguish and drive the range of NK cell functional abilities. We will discuss future areas of study that are needed to develop and test this paradigm and suggest strategies to efficiently profile NK cells based on metabolism. Given the emerging role of metabolism in driving NK cell fates, profiling and modulating NK cell metabolism holds profound therapeutic potential to tune inflammatory and regulatory NK cell responses to treat disease.
自然杀伤 (NK) 细胞能够发挥多种功能,从经典的抗肿瘤和抗病毒细胞毒性效应功能,到在控制炎症性免疫反应和促进组织生长方面的关键调节作用。然而,将 NK 细胞极化到这些截然不同和相反功能的机制尚不完全清楚。NK 细胞功能亚群主要根据表型进行鉴定和研究,这是一种用于分析 NK 细胞的便捷手段,确实提供了有关 NK 细胞激活状态的信息。然而,使用经典表型来告知功能的方法存在不一致性,这引发了以下问题:表型实际上可以定义 NK 细胞的功能命运吗?哪些因素可以分析和驱动 NK 细胞的命运?在其他免疫细胞中,细胞代谢已被证明可显著决定亚群极化。越来越多的证据表明,细胞代谢是 NK 细胞效应功能的组成部分。已证实葡萄糖驱动的糖酵解和氧化代谢可驱动经典的 NK 细胞抗肿瘤和抗病毒效应功能。最近的研究揭示了代谢在 NK 细胞发育、教育和记忆生成中的关键作用。在这篇综述中,我们将利用迄今为止的证据来研究 NK 细胞表型、代谢和功能命运之间的关系。我们探讨了一种范例,即 NK 细胞内代谢途径的差异活性产生不同的代谢特征,这些特征全面区分并驱动 NK 细胞功能能力的范围。我们将讨论未来需要开展的研究领域,以开发和测试这一范例,并提出基于代谢对 NK 细胞进行高效分析的策略。鉴于代谢在驱动 NK 细胞命运中的新兴作用,分析和调节 NK 细胞代谢具有深远的治疗潜力,可以调节炎症和调节性 NK 细胞反应,以治疗疾病。