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Malinow Molecular Methods Quantum Dots Choquet AMPAR


Study Timeline - PubMed



Summary

2003 Direct imaging of lateral movements of AMPA receptors inside synapses


Tardin, Cognet, Bats, Lounis, Choquet • 2003 • EMBO - PDF

Tested effects of glutamate and calcium influx on AMPAR diffusion.
  • Anti-GluR2 antibodies labeled with Cy5 or Alexa-647


Glutamate (100 uM) effect on GluR2
  • diffusion rate
  • (85%) endocytosis (within 15 min)
  • (55%) diffusion within synapses
  • diffusion rate non-synaptic
  • (30%) completely immobile receptors


Calcium (induced) influx effect
  • (%) mobile AMPARs
  • (59%) AMPAR membrane expression


Calcium blocking (BAPTA) effect
  • (%) mobile AMPARs


2004 Differential activity-dependent regulation of the lateral mobilities of AMPA and NMDA receptors


Groc L, Heine M, Cognet L, Brickley K, Stephenson FA, Lounis B, Choquet D. • 2004 • Nature Neuroscience - - PDF

AMPARs vs. NMDAR diffusion
  • extrasynaptic: AMPAR > NMDAR (4x)
  • synaptic: AMPAR NMDAR
  • synaptic > extrasynaptic (2x ??)
KCl Neural Stimulation
  • (5x) extrasynaptic diffusion rate AMPAR
  • (%) synaptic diffusion rate AMPAR
PKC activity (stim by TPA)
  • extrasynaptic diffusion rate AMPAR & NMDAR
  • synaptic diffusion rate AMPAR & NMDAR


2007 Diffusional trapping of GluR1 AMPA receptors by input-specific synaptic activity


Ehlers, Heine, Groc, Lee, Choquet • 2007 • Neuron - PDF

Results
  • silenced synapses had:
    • 50% less GluR1 AMPA receptors than nearby active synapses
    • no changes in PSD-95 family proteins
    • no change in presynaptic abundance of VGLUT1 or bassoon
    • no difference in PSD-95, Shank, or bassoon puncta size
  • GluR1-QDots
    • very high mobility in extrasynaptic membrane
    • intermediate mobility at inactivated synapses
    • low mobility at active synapses
    • frequently passed through several silenced synapses during recording (Movie S1)
    • often exchange from a silenced synapse to a nearby active synapse (Movie S2)
    • rarely exchanged from an active synapse to inactive synapse (2 of 1700)
    • at inactivated synapses, 76.1% of GluR1-QDs present at the synapse departed the synapse within a 60 s imaging period
    • at nearby active synapses, only 21.4% of GluR1-QDs exited the synapse within a 60 s imaging period
  • Acute Blocking of Active Synapses
    • To test whether ongoing transmitter activation of glutamate receptors was required for trapping of GluR1
    • acutely blocked (for 1-4 hr) basal spontaneous activity with TTX, AP5, and CNQX during imaging
    • blocking had no effect on GluR1 mobility at previously active or previously silenced synapses
      • synapses active before TTX/AP5/CNQX continued to exhibit decreased GluR1 mobility relative to synapses chronically silenced by tetanus toxin
    • results demonstrate the diffusional trapping of GluR1 at active synapses not acute effect of basal spontaneous activity, but rather a longer-term change in synapse organization
  • Spontaneous Activity Confines GluR1 Intrasynaptic Movement
    • in active synapses the movement of GluR1 is more confined than at inactive synapses
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(D) Single GluR1-QDs explore large areas within inactive synapses. Shown are five synaptic regions defined as a set of connected pixels obtained using object segmentation by wavelet transform. Each pixel was divided into 0.0016 mm2 subdomains and coded based on the presence (pink) or absence (white) of the GluR1-QD at any time during the imaging period as defined by the centroid of a 2D Gaussian function fit to the GluR1-QD fluorescent signal (see Experimental Procedures for details). Coded areas at each synaptic region represent the trajectory of one GluR1-QD. Scale bar, 0.2 mm. (E) GluR1 explores only small subregions within active synapses. Objects, color code, and scale bar as in (D)



2007 Interaction between Stargazin and PSD-95 Regulates AMPA Receptor Surface Trafficking


Notes
  • Quantum Dot
  • FRAP
  • Live hippocampal neurons
  • exchange of AMPAR by lateral diffusion between extrasynaptic and synaptic sites mostly depends on the interaction of Stargazin with PSD-95 and not upon the GluR2 AMPAR subunit C terminus.
  • Disruption of interactions between Stargazin and PSD-95 strongly increases AMPAR surface diffusion, preventing AMPAR accumulation at postsynaptic sites.
  • AMPARs and Stargazin diffuse as complexes in and out synapses.






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