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Interleukin-2 shapes the cytotoxic T cell proteome and immune environment–sensing programs
Author(s) -
Christina Rollings,
Linda V. Sinclair,
Hugh J.M. Brady,
Doreen A. Cantrell,
Sarah H. Ross
Publication year - 2018
Publication title -
science signaling
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.659
H-Index - 154
eISSN - 1945-0877
pISSN - 1937-9145
DOI - 10.1126/scisignal.aap8112
Subject(s) - cytotoxic t cell , immune system , proteome , cytokine , function (biology) , interleukin 2 , t cell , biology , microbiology and biotechnology , chemistry , immunology , in vitro , bioinformatics , biochemistry
Interleukin-2 (IL-2) and Janus kinases (JAKs) regulate transcriptional programs and protein synthesis to promote the differentiation of effector CD8 + cytotoxic T lymphocytes (CTLs). Using high-resolution mass spectrometry, we generated an in-depth characterization of how IL-2 and JAKs configure the CTL proteome to control CTL function. We found that IL-2 signaling through JAK1 and JAK3 (JAK1/3) increased the abundance of a key subset of proteins to induce the accumulation of critical cytokines and effector molecules in T cells. Moreover, IL-2 maintained the concentration of proteins that support core metabolic processes essential for cellular fitness. One fundamental insight was the dominant role for IL-2 in stimulating effector T cells to detect microenvironmental cues. IL-2-JAK1/3 signaling pathways thus increased the abundance of nutrient transporters, nutrient sensors, and critical oxygen-sensing molecules. These data provide key insights into how IL-2 promotes T cell function and highlight signaling mechanisms and transcription factors that integrate oxygen sensing to transcriptional control of CD8 + T cell differentiation.

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