Tuning IL-2 signaling by ADP-ribosylation of CD25

نویسندگان

  • Sophie Teege
  • Alexander Hann
  • Maria Miksiewicz
  • Cary MacMillan
  • Björn Rissiek
  • Friedrich Buck
  • Stephan Menzel
  • Marion Nissen
  • Peter Bannas
  • Friedrich Haag
  • Olivier Boyer
  • Michel Seman
  • Sahil Adriouch
  • Friedrich Koch-Nolte
چکیده

Control of immunologic tolerance and homeostasis rely on Foxp3(+)CD4(+)CD25(+) regulatory T cells (Tregs) that constitutively express the high affinity receptor for Interleukin-2, CD25. Tregs proliferate in response to injections of IL-2/anti-IL-2 antibody complexes or low doses of IL-2. However, little is known about endogenous mechanisms that regulate the sensitivity of CD25 to signaling by IL-2. Here we demonstrate that CD25 is ADP-ribosylated at Arg35 in the IL-2 binding site by ecto-ADP-ribosyltransferase ARTC2.2, a toxin-related GPI-anchored ecto-enzyme. ADP-ribosylation inhibits binding of IL-2 by CD25, IL-2- induced phosphorylation of STAT5, and IL-2-dependent cell proliferation. Our study elucidates an as-yet-unrecognized mechanism to tune IL-2 signaling. This newly found mechanism might thwart Tregs at sites of inflammation and thereby permit a more potent response of activated effector T cells.

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عنوان ژورنال:

دوره 5  شماره 

صفحات  -

تاریخ انتشار 2015