Calcium-Permeable AMPA Receptor Plasticity Is Mediated by Subunit-Specific Interactions with PICK1 and NSF

نویسندگان

  • Stephanie M. Gardner
  • Kogo Takamiya
  • Jun Xia
  • Jun-Gyo Suh
  • Richard Johnson
  • Sandy Yu
  • Richard L. Huganir
چکیده

A recently described form of synaptic plasticity results in dynamic changes in the calcium permeability of synaptic AMPA receptors. Since the AMPA receptor GluR2 subunit confers calcium permeability, this plasticity is thought to occur through the dynamic exchange of synaptic GluR2-lacking and GluR2-containing receptors. To investigate the molecular mechanisms underlying this calcium-permeable AMPA receptor plasticity (CARP), we examined whether AMPA receptor exchange was mediated by subunit-specific protein-protein interactions. We found that two GluR2-interacting proteins, the PDZ domain-containing Protein interacting with C kinase (PICK1) and N-ethylmaleimide sensitive fusion protein (NSF), are specifically required for CARP. Furthermore, PICK1, but not NSF, regulates the formation of extrasynaptic plasma membrane pools of GluR2-containing receptors that may be laterally mobilized into synapses during CARP. These results demonstrate that PICK1 and NSF dynamically regulate the synaptic delivery of GluR2-containing receptors during CARP and thus regulate the calcium permeability of AMPA receptors at excitatory synapses.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

An Essential Role for PICK1 in NMDA Receptor-Dependent Bidirectional Synaptic Plasticity

PICK1 is a calcium-sensing, PDZ domain-containing protein that interacts with GluR2 and GluR3 AMPA receptor (AMPAR) subunits and regulates their trafficking. Although PICK1 has been principally implicated in long-term depression (LTD), PICK1 overexpression in CA1 pyramidal neurons causes a CaMK- and PKC-dependent potentiation of AMPAR-mediated transmission and an increase in synaptic GluR2-lack...

متن کامل

NSF ATPase and α-/β-SNAPs Disassemble the AMPA Receptor-PICK1 Complex

Luscher et al., 1999). This indicates that NSF maintains form a complex in the presence of ATP␥S. Similar a high level of synaptic AMPARs, either by preventing to SNARE complex disassembly, NSF ATPase activity their removal by endocytosis or facilitating their insertion disrupts PICK1-GluR2 interactions in this complex. ␣-by exocytosis. The same peptide treatment occludes and ␤-SNAP have differ...

متن کامل

PICK1 is a calcium-sensor for NMDA-induced AMPA receptor trafficking.

Regulation of AMPA receptor (AMPAR) trafficking results in changes in receptor number at the postsynaptic membrane, and hence modifications in synaptic strength, which are proposed to underlie learning and memory. NMDA receptor-mediated postsynaptic Ca2+ influx enhances AMPAR internalisation, but the molecular mechanisms that trigger such trafficking are not well understood. We investigated whe...

متن کامل

Calcium binding to PICK1 is essential for the intracellular retention of AMPA receptors underlying long-term depression.

NMDA receptor (NMDAR)-dependent long-term depression (LTD) in the hippocampus is mediated primarily by the calcium-dependent removal of AMPA receptors (AMPARs) from the postsynaptic density. The AMPAR-binding, PDZ (PSD-95/Dlg/ZO1) and BAR (Bin/amphiphysin/Rvs) domain-containing protein PICK1 has been implicated in the regulation of AMPAR trafficking underlying several forms of synaptic plastici...

متن کامل

NSF ATPase and - / - SNAPs Disassemble the AMPA Receptor - PICK

Luscher et al., 1999). This indicates that NSF maintains form a complex in the presence of ATP␥S. Similar a high level of synaptic AMPARs, either by preventing to SNARE complex disassembly, NSF ATPase activity their removal by endocytosis or facilitating their insertion disrupts PICK1-GluR2 interactions in this complex. ␣-by exocytosis. The same peptide treatment occludes and ␤-SNAP have differ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Neuron

دوره 45  شماره 

صفحات  -

تاریخ انتشار 2005