53 Phosphorylation of GluR1 at PKA site can be enhanced by synapse-associated protein 97 (SAP97)/protein A kinase anchoring protein (AKAP79) complex that direct PKA to GluR1 via a PDZ (PSD95, disk large, ZO1) domain interaction.54 CAMKII pathway Numerous studies have demonstrated that CAMKII is required for the proper formation of LTP in slice preparations, and in regulating learning and memory in rodents.55 In response to stimulation,

CAMKII translocates to the postsynaptic site, where it has two major effects on AMPA receptor Inhibitors,research,lifescience,medical activity at the postsynaptic site during the formation of LTP.55 First, the AMPA single conductance is directly increased by CAMKII at Ser831 of GluR1 subunit.56 Second, CAMKII is required for the delivery of AMPA receptor to the synapse, which is lacking AMPA receptors.51,57,58 This enhancement of synaptic GluR1 level by activation of CAMKII requires an intact C-terminal domain of GluR1 , and is possibly involved in

interaction with SAP97.59 Inhibitors,research,lifescience,medical PP1, which is also known to be a important modulator for learning and memory, can dephosphorylate the phosphorylation of GluR1 at p831 site by CAMKII.60 Extracellular signal-regulated kinase (ERK) MAPK pathway A recent study reported that the small guananine triphosphatases Inhibitors,research,lifescience,medical (GTPases) Ras and Rap are involved in AMPA receptor trafficking through a postsynaptic signaling mechanism. Ras mediates activity-evoked increase in GluR1/GluR4-containing AMPA receptor surface expression at synapses via a pathway that requires p42/44 MAPK activation. Inhibitors,research,lifescience,medical In contrast, Rap mediates NMDA-dependent removal of synaptic GluR2/GluR3-containing vesicles via a pathway that involves p38 MAPK. The regulation through Ras and Rap, which work as molecular switches, may in turn control the AMPA receptor level at synapses.61 PKC pathways AMPA GluR2 receptors respond to secondary signals by constitutive receptor recycling. Phosphorylation of Ser880 on GluR2 provides a

switch from receptor retention at the membrane by binding to ABP (AMPA receptor-binding protein)/GRIP (glutamate receptor-interacting protein), to receptor internalization Inhibitors,research,lifescience,medical by binding to PICK 1 (protein interacting with Endonuclease C kinase-1). Therefore, phosphorylation of GluR2 at Ser880 by PKC may release the AMPA receptor from the anchoring proteins and initiate the internalization of receptors.62-65 The mechanism for AMPA receptor trafficking is specific for brain region and neuronal type. For example, the endocytosis of AMPA receptors mediating LTD is triggered by very www.selleckchem.com/Tie2-kinase.html different signaling cascades in different cell types despite the fact that a conserved cell biological mechanism (ie, clathrin/dynamine-dependent endocytosis) always seems to be involved. Specifically, in CA1 pyramidal cells, protein phosphatases seem to be involved in triggering LTD through dephosphorylation of GluR1 and phosphorylation of PKA site on GluR1 is associated with LTP.