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Synaptic PRG-1 Modulates Excitatory Transmission via Lipid Phosphate-Mediated Signaling

  作者 Trimbuch, T; Beed, P; Vogt, J; Schuchmann, S; Maier, N; Kintscher, M; Breustedt, J; Schuelke, M; Streu, N; Kieselmann, O; Brunk, I; Laube, G; Strauss, U; Battefeld, A; Wende, H; Birchmeier, C; Wiese, S; Sendtner, M; Kawabe, H; Kishimoto-Suga, M; Brose, N; Baumgart, J; Geist, B; Aoki, J; Savaskan, NE; Brauer, AU; Chun, J; Ninnemann, O; Schmitz, D; Nitsch, R  
  选自 期刊  Cell;  卷期  2009年138-6;  页码  1222-1235  
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[摘要]Plasticity related gene-1 (PRG-1) is a brain-specific membrane protein related to lipid phosphate phosphatases, which acts in the hippocampus specifically at the excitatory synapse terminating on glutamatergic neurons. Deletion of prg-1 in mice leads to epileptic seizures and augmentation of EPSCs, but not IPSCs. In utero electroporation of PRG-1 into deficient animals revealed that PRG-1 modulates excitation at the synaptic junction. Mutation of the extracellular domain of PRG-1 crucial for its interaction with lysophosphatidic acid (LPA) abolished the ability to prevent hyperexcitability. As LPA application in vitro induced hyperexcitability in wild-type but not in LPA(2) receptor-deficient animals, and uptake of phospholipids is reduced in PRG-1-deficient neurons, we assessed PRG-1/LPA(2) receptor deficient animals, and found that the pathophysiology observed in the PRG-1-deficient mice was fully reverted. Thus, we propose PRG-1 as an important player in the modulatory control of hippocampal excitability dependent on presynaptic LPA(2) receptor signaling.

 
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