. PAR-1 kinase phosphorylates Dlg and regulates its postsynaptic targeting at the Drosophila neuromuscular junction. Neuron. 2007 Jan 18;53(2):201-15. PubMed.

Recommends

Please login to recommend the paper.

Comments

Make a Comment

To make a comment you must login or register.

Comments on this content

  1. This study convincingly demonstrates that PAR-1 phosphorylation of Dlg reduces the amount of Dlg localized to postsynaptic sites, and consequently decreases excitatory transmission. PAR-1 and Dlg are the fly homologs of mammalian proteins MARK and PSD-95, respectively. In mice, knocking out PSD-95 decreases excitatory transmission through the selective removal of AMPA-type glutamate receptors at synapses (Beique et al., 2006). Curiously, elevated levels of amyloid-β have been linked to reductions in levels of synaptic PSD-95 (Gylys et al., 2004; Almeida et al., 2005; Roselli et al., 2005) and surface AMPA receptors (Almeida et al., 2005; Roselli et al., 2005; Hsieh et al., 2006), and also to depression of AMPA receptor-mediated synaptic transmission (Kamenetz et al., 2003; Hsieh et al., 2006; Ting et al., 2006). Together these findings raise the possibility that elevated levels of amyloid-β could be decreasing excitatory transmission in AD by activating MARK, leading to phosphorylation of PSD-95 and subsequent removal of synaptic AMPA receptors.

    Although PAR-1/MARK have been shown to phosphorylate tau, this does not seem to be playing a role in the synaptic effects observed by Zhang et al., because effects of PAR-1 upregulation were blocked by expression of a non-phosphorylatable variant of Dlg, and were reproduced by expression of a phospho-mimetic variant of Dlg.

    References:

    . Beta-amyloid accumulation in APP mutant neurons reduces PSD-95 and GluR1 in synapses. Neurobiol Dis. 2005 Nov;20(2):187-98. PubMed.

    . Synapse-specific regulation of AMPA receptor function by PSD-95. Proc Natl Acad Sci U S A. 2006 Dec 19;103(51):19535-40. PubMed.

    . Synaptic changes in Alzheimer's disease: increased amyloid-beta and gliosis in surviving terminals is accompanied by decreased PSD-95 fluorescence. Am J Pathol. 2004 Nov;165(5):1809-17. PubMed.

    . AMPAR removal underlies Abeta-induced synaptic depression and dendritic spine loss. Neuron. 2006 Dec 7;52(5):831-43. PubMed.

    . APP processing and synaptic function. Neuron. 2003 Mar 27;37(6):925-37. PubMed.

    . Soluble beta-amyloid1-40 induces NMDA-dependent degradation of postsynaptic density-95 at glutamatergic synapses. J Neurosci. 2005 Nov 30;25(48):11061-70. PubMed.

    . Amyloid precursor protein overexpression depresses excitatory transmission through both presynaptic and postsynaptic mechanisms. Proc Natl Acad Sci U S A. 2007 Jan 2;104(1):353-8. PubMed.

This paper appears in the following:

News

  1. Synapses MARKed for Failure After PSD-95 Phosphorylation