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      The Glycerophosphoinositols: From Lipid Metabolites to Modulators of T-Cell Signaling

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          Abstract

          Glycerophosphoinositols (GPIs) are bioactive, diffusible phosphoinositide metabolites of phospholipase A 2 that act both intracellularly and in a paracrine fashion following their uptake by specific transporters. The most representative compound, glycerophosphoinositol (GroPIns), is a ubiquitous component of eukaryotic cells that participates in central processes, including cell proliferation and survival. Moreover, glycerophosphoinositol 4-phosphate (GroPIns4 P) controls actin dynamics in several cell systems by regulating Rho GTPases. Recently, immune cells have emerged as targets of the biological activities of the GPIs. We have shown that exogenous GroPIns4 P enhances CXCL12-induced T-cell chemotaxis through activation of the kinase Lck in a cAMP/PKA-dependent manner. While highlighting the potential of GroPIns4 P as an immunomodulator, this finding raises questions on the role of endogenously produced GroPIns4 P as well as of other GPIs in the regulation of the adaptive immune responses under homeostatic and pathological settings. Here we will summarize our current understanding of the biological activities of the GPIs, with a focus on lymphocytes, highlighting open questions and potential developments in this promising new area.

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          Most cited references46

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          Biology of the p21-activated kinases.

          The p21-activated kinases (PAKs) 1-3 are serine/threonine protein kinases whose activity is stimulated by the binding of active Rac and Cdc42 GTPases. Our understanding of the regulation and biology of these important signaling proteins has increased tremendously since their discovery in the mid-1990s. PAKs 1-3 are activated by a variety of GTPase-dependent and -independent mechanisms. This complexity reflects the contributions of PAK function in many cellular signaling pathways and the need to carefully control PAK action in a highly localized manner. PAKs serve as important regulators of cytoskeletal dynamics and cell motility, transcription through MAP kinase cascades, death and survival signaling, and cell-cycle progression. Consequently, PAKs have also been implicated in a number of pathological conditions and in cell transformation. We propose here a key role for PAK action in coordinating the dynamics of the actin and microtubule cytoskeletons during directional motility of cells, as well as in other functions requiring cytoskeletal polarization.
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            Genetic evidence for the involvement of the lck tyrosine kinase in signal transduction through the T cell antigen receptor.

            Signaling through the T cell antigen receptor (TCR) results both in rapid increases in tyrosine phosphorylation on a number of proteins and in the activation of the phosphatidylinositol pathway. It is not clear how stimulation of the TCR leads to these signaling events. Mutants of the Jurkat T cell line have been previously isolated that fail to show increases in calcium following receptor stimulation. Analysis of one of these mutants, JCaM1, which is defective in the induction of tyrosine phosphorylation, revealed a defect in the expression of functional lck tyrosine kinase. The lack of lck activity was caused in part by a splicing defect. Expression of the lck cDNA in JCaM1 restores the ability of the cell to respond to TCR stimulation. These results indicate that lck is required for normal signal transduction through the TCR.
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              T-cell receptor proximal signaling via the Src-family kinases, Lck and Fyn, influences T-cell activation, differentiation, and tolerance.

              T-cell development in the thymus and activation of mature T cells in secondary lymphoid organs requires the ability of cells to respond appropriately to environmental signals at multiple stages of their development. The process of thymocyte selection insures a functional T-cell repertoire, while activation of naive peripheral T cells induces proliferation, gain of effector function, and, ultimately, long-lived T-cell memory. The T-cell immune response is initiated upon engagement of the T-cell receptor (TCR) and coreceptor, CD4 or CD8, by cognate antigen/major histocompatibility complexes presented by antigen-presenting cells. TCR/coreceptor engagement induces the activation of biochemical signaling pathways that, in combination with signals from costimulator molecules and cytokine receptors, direct the outcome of the response. Activation of the src-family kinases p56(lck) (Lck) and p59(fyn) (Fyn) is central to the initiation of TCR signaling pathways. This review focuses on our current understanding of the mechanisms by which these two proteins orchestrate T-cell function.
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                Author and article information

                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                24 April 2013
                29 July 2013
                2013
                : 4
                : 213
                Affiliations
                [1] 1Department of Life Sciences, University of Siena Siena Italy
                [2] 2Institute of Protein Biochemistry, National Research Council Naples, Italy
                Author notes

                Edited by: Klaus Okkenhaug, Babraham Institute, UK

                Reviewed by: Sho Yamasaki, Kyushu University, Japan; Karsten Sauer, The Scripps Research Institute, USA

                *Correspondence: Laura Patrussi, Department of Life Sciences, University of Siena, Via Aldo Moro 2, 53100 Siena, Italy e-mail: patrussi2@ 123456unisi.it ; Stefania Mariggiò, Institute of Protein Biochemistry, National Research Council, Via Pietro Castellino 111, 80131 Naples, Italy e-mail: s.mariggio@ 123456ibp.cnr.it

                This article was submitted to Frontiers in T Cell Biology, a specialty of Frontiers in Immunology.

                Article
                10.3389/fimmu.2013.00213
                3725514
                23908653
                8a27602b-35fd-466e-bf4a-63abb09e3e48
                Copyright © 2013 Patrussi, Mariggiò, Corda and Baldari.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.

                History
                : 29 March 2013
                : 11 July 2013
                Page count
                Figures: 2, Tables: 0, Equations: 0, References: 49, Pages: 6, Words: 0
                Categories
                Immunology
                Perspective Article

                Immunology
                glycerophosphoinositol,t-cell chemotaxis,cxcl12,lck
                Immunology
                glycerophosphoinositol, t-cell chemotaxis, cxcl12, lck

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