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      The PI3K Pathway in B Cell Metabolism

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          Abstract

          B cell growth and proliferation is tightly regulated by signaling through the B cell receptor and by other membrane bound receptors responding to different cytokines. The PI3K signaling pathway has been shown to play a crucial role in B cell activation, differentiation and survival. Activated B cells undergo metabolic reprogramming in response to changing energetic and biosynthetic demands. B cells also need to be able to coordinate metabolic activity and proliferation with nutrient availability. The PI3K signaling network has been implicated in regulating nutrient acquisition, utilization and biosynthesis, thus integrating receptor mediated signaling with cell metabolism. In this review, we discuss the current knowledge about metabolic changes induced in activated B cells, strategies to adapt to metabolic stress and the role of PI3K signaling in these processes.

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          Author and article information

          Journal
          8903774
          3208
          Crit Rev Biochem Mol Biol
          Crit. Rev. Biochem. Mol. Biol.
          Critical reviews in biochemistry and molecular biology
          1040-9238
          1549-7798
          30 November 2016
          05 August 2016
          September 2016
          01 September 2017
          : 51
          : 5
          : 359-378
          Affiliations
          [1 ]BIOSS Centre for Biological Signalling Studies, Albert-Ludwigs-University Freiburg, Schänzlestr. 18, 79104 Freiburg, Germany
          [2 ]Max Planck Institute of Immunobiology and Epigenetics, Stübeweg 51, 79108 Freiburg, Germany
          [3 ]Sanford Burnham Prebys Medical Discovery Institute, 10901 N. Torrey Pines Road, La Jolla, CA 92037
          Author notes
          [* ]Corresponding author, Phone: (858) 646-3153, robert@ 123456SBPdiscovery.org
          Article
          PMC5139348 PMC5139348 5139348 nihpa832271
          10.1080/10409238.2016.1215288
          5139348
          27494162
          60440288-0ae8-4e80-bad6-9f6a3e297a21
          History
          Categories
          Article

          Akt,mitochondria,glycolysis,lymphocyte,mTOR
          Akt, mitochondria, glycolysis, lymphocyte, mTOR

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