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10.1080/15384101.2016.1156267

http://scihub22266oqcxt.onion/10.1080/15384101.2016.1156267
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C4889261!4889261!26940341
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suck abstract from ncbi


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pmid26940341      Cell+Cycle 2016 ; 15 (8): 1073-83
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  • T cell proliferation and adaptive immune responses are critically regulated by protein phosphatase 4 #MMPMID26940341
  • Liao FH; Hsiao WY; Lin YC; Chan YC; Huang CY
  • Cell Cycle 2016[]; 15 (8): 1073-83 PMID26940341show ga
  • The clonal expansion of activated T cells is pivotal for the induction of protective immunity. Protein phosphatase 4 (PP4) is a ubiquitously expressed serine/threonine phosphatase with reported functions in thymocyte development and DNA damage responses. However, the role of PP4 in T cell immunity has not been thoroughly investigated. In this report, our data showed that T cell-specific ablation of PP4 resulted in defective adaptive immunity, impaired T cell homeostatic expansion, and inefficient T cell proliferation. This hypo-proliferation was associated with a partial G1-S cell cycle arrest, enhanced transcriptions of CDK inhibitors and elevated activation of AMPK. In addition, resveratrol, a known AMPK activator, induced similar G1-S arrests, while lentivirally-transduced WT or constitutively-active AMPK?1 retarded the proliferation of WT T cells. Further investigations showed that PP4 co-immunoprecipitated with AMPK?1, and the over-expression of PP4 inhibited AMPK phosphorylation, thereby implicating PP4 for the negative regulation of AMPK. In summary, our results indicate that PP4 is an essential modulator for T cell proliferation and immune responses; they further suggest a potential link between PP4 functions, AMPK activation and G1-S arrest in activated T cells.
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