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Interleukin-12 bypasses common gamma-chain signalling in emergency natural killer cell lymphopoiesis.


ABSTRACT: Differentiation and homeostasis of natural killer (NK) cells relies on common gamma-chain (?c)-dependent cytokines, in particular IL-15. Consequently, NK cells do not develop in mice with targeted ?c deletion. Herein we identify an alternative pathway of NK-cell development driven by the proinflammatory cytokine IL-12, which can occur independently of ?c-signalling. In response to viral infection or upon exogenous administration, IL-12 is sufficient to elicit the emergence of a population of CD122+CD49b+ cells by targeting NK-cell precursors (NKPs) in the bone marrow (BM). We confirm the NK-cell identity of these cells by transcriptome-wide analyses and their ability to eliminate tumour cells. Rather than using the conventional pathway of NK-cell development, IL-12-driven CD122+CD49b+ cells remain confined to a NK1.1lowNKp46low stage, but differentiate into NK1.1+NKp46+ cells in the presence of ?c-cytokines. Our data reveal an IL-12-driven hard-wired pathway of emergency NK-cell lymphopoiesis bypassing steady-state ?c-signalling.

SUBMITTER: Ohs I 

PROVIDER: S-EPMC5172358 | biostudies-literature | 2016 Dec

REPOSITORIES: biostudies-literature

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Interleukin-12 bypasses common gamma-chain signalling in emergency natural killer cell lymphopoiesis.

Ohs Isabel I   van den Broek Maries M   Nussbaum Kathrin K   Münz Christian C   Arnold Sebastian J SJ   Quezada Sergio A SA   Tugues Sonia S   Becher Burkhard B  

Nature communications 20161216


Differentiation and homeostasis of natural killer (NK) cells relies on common gamma-chain (γc)-dependent cytokines, in particular IL-15. Consequently, NK cells do not develop in mice with targeted γc deletion. Herein we identify an alternative pathway of NK-cell development driven by the proinflammatory cytokine IL-12, which can occur independently of γc-signalling. In response to viral infection or upon exogenous administration, IL-12 is sufficient to elicit the emergence of a population of CD1  ...[more]

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