4.8 Article

Natural Killer Cell Education Is Associated With a Distinct Glycolytic Profile

Journal

FRONTIERS IN IMMUNOLOGY
Volume 9, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2018.03020

Keywords

HLA class I; metabolism; NK-cell education; glycolysis; Glut1; killer-cell immunoglobulin-like receptor (KIR); cytotoxicity

Categories

Funding

  1. Heinrich Pette Institute
  2. European Union's Horizon 2020 research and innovation programme [681032]
  3. Swiss government (through the State Secretariat for Education, Research and Innovation, SERI) [15.0337]
  4. H2020 Societal Challenges Programme [681032] Funding Source: H2020 Societal Challenges Programme

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NK cells expressing self-inhibitory receptors display increased functionality compared to NK cells lacking those receptors. The acquisition of functional competence in these particular NK-cell subsets is termed education. Little is known about the underlying mechanisms that lead to the functional differences between educated and uneducated NK cells. An increasing number of studies suggest that cellular metabolism is a determinant of immune cell functions. Thus, alterations in cellular metabolic pathways may play a role in the process of NK-cell education. Here, we compared the glycolytic profile of educated and uneducated primary human NK cells. KIR-educated NK cells showed significantly increased expression levels of the glucose transporter Glut1 in comparison to NKG2A-educated or uneducated NK cells with and without exposure to target cells. Subsequently, the metabolic profile of NK-cell subsets was determined using a Seahorse XF Analyzer. Educated NK cells displayed significantly higher rates of cellular glycolysis than uneducated NK cells even in a resting state. Our results indicate that educated and uneducated NK cells reside in different metabolic states prior to activation. These differences in the ability to utilize glucose may represent an underlying mechanism for the superior functionality of educated NK cells expressing self-inhibitory receptors.

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