Intra-lineage Plasticity and Functional Reprogramming Maintain Natural Killer Cell Repertoire Diversity
Aline Pfefferle(Karolinska Institutet), Bénédikt Jacobs(Oslo University Hospital), Herman Netskar(Oslo University Hospital), Eivind Heggernes Ask(University of Oslo), Susanne Lorenz(Oslo University Hospital), Trevor Clancy(University of Oslo), Jodie P. Goodridge(Fate Therapeutics (United States)), Ebba Sohlberg(Karolinska Institutet), Karl‐Johan Malmberg(Oslo University Hospital)
Cited by 51Open Access
Abstract
NK cells with an induced CD57 phenotype display increased functional potential associated with increased transcription of genes involved in adhesion and immune synapse formation. Rapidly cycling cells upregulate NKG2A, display a general loss of functionality, and a transcriptional signature associated with increased apoptosis/cellular stress, actin-remodeling, and nuclear factor κB (NF-κB) activation. These results shed light on the role of intra-lineage plasticity during NK cell homeostasis and suggest that the functional fate of the cell is tightly linked to the acquired phenotype and transcriptional reprogramming.
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