The Strength of Receptor Signaling Is Centrally Controlled through a Cooperative Loop between Ca2+ and an Oxidant Signal

Activation of cell-surface receptors stimulates generation of intracellular signals that, in turn, direct the cellular response. However, mechanisms that ensure combinatorial control of these signaling events are not well understood. We show here that the Ca2+ and reactive oxygen intermediates generated upon BCR activation rapidly engage in a cooperative interaction that acts in a feedback manner to amplify the early signal generated. This cooperativity acts by regulating the concentration of the oxidant produced. The latter exerts its influence through a pulsed inactivation of receptor-coupled phosphatases, where the amplitude of this pulse is determined by oxidant concentration. The extent of phosphatase inhibition, in turn, dictates what proportion of receptor-proximal kinases are activated and, as a result, the net strength of the initial signal. It is the strength of this initial signal that finally determines the eventual duration of BCR signaling and the rate of its transmission through downstream pathways.

[1]  Tilman Brummer,et al.  Feedback regulation of lymphocyte signalling , 2004, Nature Reviews Immunology.

[2]  Z. Zhang,et al.  Protein-tyrosine phosphatases: biological function, structural characteristics, and mechanism of catalysis. , 1998, Critical reviews in biochemistry and molecular biology.

[3]  T. Pawson,et al.  Signaling through scaffold, anchoring, and adaptor proteins. , 1997, Science.

[4]  Michael Reth,et al.  Hydrogen peroxide as second messenger in lymphocyte activation , 2002, Nature Immunology.

[5]  J. Monroe,et al.  Basal B‐cell receptor signaling in B lymphocytes: mechanisms of regulation and role in positive selection, differentiation, and peripheral survival , 2004, Immunological reviews.

[6]  Tony Pawson,et al.  Signaling Networks—Do All Roads Lead to the Same Genes? , 1999, Cell.

[7]  J. Lambeth,et al.  Novel homologs of gp91phox. , 2000, Trends in biochemical sciences.

[8]  M. Reth,et al.  Monomeric and oligomeric complexes of the B cell antigen receptor. , 2000, Immunity.

[9]  D. Kufe,et al.  Negative regulation of the SHPTP1 protein tyrosine phosphatase by protein kinase C delta in response to DNA damage. , 2001, Molecular pharmacology.

[10]  L. Zhu,et al.  Insulin-stimulated Hydrogen Peroxide Reversibly Inhibits Protein-tyrosine Phosphatase 1B in Vivo and Enhances the Early Insulin Action Cascade* , 2001, The Journal of Biological Chemistry.

[11]  T. Finkel Oxidant signals and oxidative stress. , 2003, Current opinion in cell biology.

[12]  K. Krause,et al.  A Ca2+-activated NADPH Oxidase in Testis, Spleen, and Lymph Nodes* , 2001, The Journal of Biological Chemistry.

[13]  L. Oberley,et al.  Discrete Generation of Superoxide and Hydrogen Peroxide by T Cell Receptor Stimulation , 2002, The Journal of experimental medicine.

[14]  B. Bánfi,et al.  Mechanism of Ca 2 Activation of the NADPH Oxidase 5 ( NOX 5 ) * □ S , 2004 .

[15]  A. Görg,et al.  The current state of two‐dimensional electrophoresis with immobilized pH gradients , 2000, Electrophoresis.

[16]  D. Alexander,et al.  The CD45 tyrosine phosphatase: a positive and negative regulator of immune cell function. , 2000, Seminars in immunology.

[17]  Reinhart Heinrich,et al.  Mathematical models of protein kinase signal transduction. , 2002, Molecular cell.

[18]  B. Sefton,et al.  Association between B-lymphocyte membrane immunoglobulin and multiple members of the Src family of protein tyrosine kinases , 1992, Molecular and cellular biology.

[19]  J. Kwon,et al.  T cells express a phagocyte-type NADPH oxidase that is activated after T cell receptor stimulation , 2004, Nature Immunology.

[20]  K. Krause,et al.  Mechanism of Ca2+ Activation of the NADPH Oxidase 5 (NOX5)* , 2004, Journal of Biological Chemistry.

[21]  S. Rhee,et al.  Reversible Inactivation of Protein-tyrosine Phosphatase 1B in A431 Cells Stimulated with Epidermal Growth Factor* , 1998, The Journal of Biological Chemistry.

[22]  J. Ferrell Self-perpetuating states in signal transduction: positive feedback, double-negative feedback and bistability. , 2002, Current opinion in cell biology.

[23]  J. Kinet,et al.  BTK regulates PtdIns-4,5-P2 synthesis: importance for calcium signaling and PI3K activity. , 2003, Immunity.

[24]  John D. Scott,et al.  Signaling Complexes: Junctions on the Intracellular Information Super Highway , 2002, Current Biology.

[25]  Keli Xu,et al.  Calcium oscillations increase the efficiency and specificity of gene expression , 1998, Nature.

[26]  T. Tanaka,et al.  Mechanism of H2O2 production in porcine thyroid cells: evidence for intermediary formation of superoxide anion by NADPH-dependent H2O2-generating machinery. , 1991, Biochemistry.

[27]  J. Neilson,et al.  Calcium signalling in lymphocytes. , 2003, Current opinion in immunology.

[28]  A. Bhattacharya,et al.  Characterization of EhCaBP, a calcium-binding protein of Entamoeba histolytica and its binding proteins. , 1997, Molecular and biochemical parasitology.

[29]  D. Jackson,et al.  Recruitment and Activation of SHP-1 Protein-tyrosine Phosphatase by Human Platelet Endothelial Cell Adhesion Molecule-1 (PECAM-1) , 1998, The Journal of Biological Chemistry.

[30]  U. Bhalla,et al.  Emergent properties of networks of biological signaling pathways. , 1999, Science.

[31]  G. Mills,et al.  Identification of the tyrosine phosphatase PTP1C as a B cell antigen receptor-associated protein involved in the regulation of B cell signaling , 1995, The Journal of experimental medicine.

[32]  U. Bhalla,et al.  Complexity in biological signaling systems. , 1999, Science.

[33]  T. Kurosaki Regulation of B cell fates by BCR signaling components. , 2002, Current opinion in immunology.

[34]  Toshiyuki Fukada,et al.  Reversible oxidation and inactivation of protein tyrosine phosphatases in vivo. , 2002, Molecular cell.

[35]  Y. Kubohara,et al.  The putative morphogen, DIF-1, of Dictyostelium discoideum activates Akt/PKB in human leukemia K562 cells. , 1999, Biochemical and biophysical research communications.

[36]  Takashi Morii,et al.  Amplification of receptor signalling by Ca2+ entry‐mediated translocation and activation of PLCγ2 in B lymphocytes , 2003, The EMBO journal.

[37]  D. Kufe,et al.  Negative Regulation of the SHPTP 1 Protein Tyrosine Phosphatase by Protein Kinase C in Response to DNA Damage , 2001 .

[38]  E. Stadtman,et al.  Regulation of oxidative stress-induced calcium release by phosphatidylinositol 3-kinase and Bruton's tyrosine kinase in B cells. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[39]  T. Kurosaki,et al.  BLNK: connecting Syk and Btk to calcium signals. , 2000, Immunity.

[40]  R. Soberman,et al.  Specificity of a third kind : reactive oxygen and nitrogen intermediates in cell signaling , 2022 .