A PP4 Holoenzyme Balances Physiological and Oncogenic Nuclear Factor-Kappa B Signaling in T Lymphocytes

作者：Brechmann Markus; Mock Thomas; Nickles Dorothee; Kiessling Michael; Weit Nicole; Breuer Rebecca; Mueller Wolfgang; Wabnitz Guido; Frey Felice; Nicolay Jan P; Booken Nina; Samstag Yvonne; Klemke Claus Detlev; Herling Marco; Boutros Michael; Krammer Peter H; Arnold Ruediger^*

来源：Immunity, 2012, 37(4): 697-708.

DOI：10.1016/j.immuni.2012.07.014

Signal transduction to nuclear factor-kappa B (NE-kappa B) involves multiple kinases and phosphorylated target proteins, but little is known about signal termination by dephosphorylation. By RNAi screening, we have identified protein phosphatase 4 regulatory subunit 1 (PP4R1) as a negative regulator of NF-kappa B activity in T lymphocytes. PP4R1 formed part of a distinct PP4 holoenzyme and bridged the inhibitor of NF-kappa B kinase (IKK) complex and the phosphatase PP4c, thereby directing PP4c activity to dephosphorylate and inactivate the IKK complex. PP4R1 expression was triggered upon activation and proliferation of primary human T lymphocytes and deficiency for PP4R1 caused sustained and increased IKK activity, T cell hyperactivation, and aberrant NF-kappa B signaling in NF-kappa B-addicted T cell lymphomas. Collectively, our results unravel PP4R1 as a previously unknown activation-associated negative regulator of IKK activity in lymphocytes whose downregulation promotes oncogenic NE-kappa B signaling in a subgroup of T cell lymphomas.

• 出版日期2012-10-19