A. J. Borgdorff and D. Choquet, Regulation of AMPA receptor lateral movements, Nature, vol.17, issue.6889, pp.649-653, 2002.
DOI : 10.1016/S0959-4388(00)00099-4

L. Groc, Differential activity-dependent regulation of the lateral mobilities of AMPA and NMDA receptors, Nature Neuroscience, vol.20, issue.7, pp.695-696, 2004.
DOI : 10.1016/S0896-6273(00)00129-X

M. Heine, Surface Mobility of Postsynaptic AMPARs Tunes Synaptic Transmission, Science, vol.320, issue.5873, pp.201-205, 2008.
DOI : 10.1126/science.1152089
URL : https://hal.archives-ouvertes.fr/hal-00747627

L. Bard, Dynamic and specific interaction between synaptic NR2-NMDA receptor and PDZ proteins, Proc. Natl Acad. Sci. USA, pp.19561-19566, 2010.
DOI : 10.1073/pnas.1002690107

J. P. Dupuis, Surface dynamics of GluN2B-NMDA receptors controls plasticity of maturing glutamate synapses, The EMBO Journal, vol.33, issue.8, pp.842-861, 2014.
DOI : 10.1002/embj.201386356

L. Groc, NMDA receptor surface mobility depends on NR2A-2B subunits, Proc. Natl Acad. Sci. USA 103, pp.18769-18774, 2006.
DOI : 10.1073/pnas.0605238103
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1693737

J. Meier, C. Vannier, A. Sergé, A. Triller, and D. Choquet, Fast and reversible trapping of surface glycine receptors by gephyrin, Nature Neuroscience, vol.4, issue.3, pp.253-260, 2001.
DOI : 10.1038/85099

H. Bannai, Activity-Dependent Tuning of Inhibitory Neurotransmission Based on GABAAR Diffusion Dynamics, Neuron, vol.62, issue.5, pp.670-682, 2009.
DOI : 10.1016/j.neuron.2009.04.023

L. Ladepeche, L. Yang, D. Bouchet, and L. Groc, Regulation of Dopamine D1 Receptor Dynamics within the Postsynaptic Density of Hippocampal Glutamate Synapses, PLoS ONE, vol.3, issue.9, p.74512, 2013.
DOI : 10.1371/journal.pone.0074512.g004

L. Ladepeche, Single-molecule imaging of the functional crosstalk between surface NMDA and dopamine D1 receptors, Proc. Natl Acad. Sci. USA, pp.18005-18010, 2013.
DOI : 10.1073/pnas.1310145110
URL : https://hal.archives-ouvertes.fr/hal-01289961

D. Choquet and A. Triller, The Dynamic Synapse, Neuron, vol.80, issue.3, pp.691-703, 2013.
DOI : 10.1016/j.neuron.2013.10.013

M. Maglione and S. J. Sigrist, Seeing the forest tree by tree: super-resolution light microscopy meets the neurosciences, Nature Neuroscience, vol.186, issue.7, pp.790-797, 2013.
DOI : 10.1002/anie.201200853

S. Lévi, M. Dahan, and A. Triller, Labeling Neuronal Membrane Receptors with Quantum Dots, Cold Spring Harbor Protocols, vol.2011, issue.3, p.5580, 2011.
DOI : 10.1101/pdb.prot5580

L. Groc, Surface Trafficking of Neurotransmitter Receptor: Comparison between Single-Molecule/Quantum Dot Strategies, Journal of Neuroscience, vol.27, issue.46, pp.12433-12437, 2007.
DOI : 10.1523/JNEUROSCI.3349-07.2007

B. Biermann, Imaging of molecular surface dynamics in brain slices using single-particle tracking, Nature Communications, vol.22, p.3024, 2014.
DOI : 10.1038/ncomms4024

M. F. Bennewitz and W. M. Saltzman, Nanotechnology for delivery of drugs to the brain for epilepsy, Neurotherapeutics, vol.127, issue.4, pp.323-336, 2009.
DOI : 10.1016/j.nurt.2009.01.018

J. Kreuter, Mechanism of polymeric nanoparticle-based drug transport across the blood-brain barrier (BBB), Journal of Microencapsulation, vol.137, issue.1, pp.49-54, 2012.
DOI : 10.3109/1061186X.2010.513712

K. K. Jain, Nanobiotechnology-based strategies for crossing the blood???brain barrier, Nanomedicine, vol.7, issue.8, pp.1225-1233, 2012.
DOI : 10.2217/nnm.12.86

C. Missale, S. R. Nash, S. W. Robinson, M. Jaber, and M. G. Caron, Dopamine receptors: from structure to function, Physiol. Rev, vol.78, pp.189-225, 1998.

R. A. Wise and . Dopamine, Dopamine, learning and motivation, Nature Reviews Neuroscience, vol.22, issue.6, pp.483-494, 2004.
DOI : 10.1016/0006-8993(91)91263-Z

L. Scott, Allosteric changes of the NMDA receptor trap diffusible dopamine 1 receptors in spines, Proc. Natl Acad. Sci. USA 103, pp.762-767, 2006.

G. Porras, PSD-95 expression controls l-DOPA dyskinesia through dopamine D1 receptor trafficking, Journal of Clinical Investigation, vol.122, issue.11, pp.3977-3989, 2012.
DOI : 10.1172/JCI59426DS1
URL : https://hal.archives-ouvertes.fr/hal-00956903

L. Ladépêche, J. P. Dupuis, and L. Groc, Surface trafficking of NMDA receptors: Gathering from a partner to another, Seminars in Cell & Developmental Biology, vol.27, pp.3-13, 2014.
DOI : 10.1016/j.semcdb.2013.10.005

C. Nicholson and L. Tao, Hindered diffusion of high molecular weight compounds in brain extracellular microenvironment measured with integrative optical imaging, Biophysical Journal, vol.65, issue.6, pp.2277-2290, 1993.
DOI : 10.1016/S0006-3495(93)81324-9

M. Dahan, Diffusion Dynamics of Glycine Receptors Revealed by Single-Quantum Dot Tracking, Science, vol.302, issue.5644, pp.442-445, 2003.
DOI : 10.1126/science.1088525
URL : https://hal.archives-ouvertes.fr/hal-00002449

M. Mondin, Neurexin-Neuroligin Adhesions Capture Surface-Diffusing AMPA Receptors through PSD-95 Scaffolds, Journal of Neuroscience, vol.31, issue.38, pp.13500-13515, 2011.
DOI : 10.1523/JNEUROSCI.6439-10.2011

C. Tardin, L. Cognet, C. Bats, B. Lounis, and D. Choquet, Direct imaging of lateral movements of AMPA receptors inside synapses, The EMBO Journal, vol.22, issue.18, pp.4656-4665, 2003.
DOI : 10.1093/emboj/cdg463
URL : https://hal.archives-ouvertes.fr/hal-00143981

V. Zastrow, M. Williams, and J. , Modulating neuromodulation by receptor membrane traffic in the endocytic pathway, Neuron, vol.76, pp.22-32, 2012.

L. Groc, D. Choquet, and F. Chaouloff, The stress hormone corticosterone conditions AMPAR surface trafficking and synaptic potentiation, Nature Neuroscience, vol.131, issue.8, pp.868-870, 2008.
DOI : 10.1038/nn.2150

K. Gerrow and A. Triller, Synaptic stability and plasticity in a floating world, Current Opinion in Neurobiology, vol.20, issue.5, pp.631-639, 2010.
DOI : 10.1016/j.conb.2010.06.010

M. Bruchez, M. Moronne, P. Gin, S. Weiss, and A. P. Alivisatos, Semiconductor Nanocrystals as Fluorescent Biological Labels, Science, vol.281, issue.5385, pp.2013-2016, 1998.
DOI : 10.1126/science.281.5385.2013

X. Michalet, Quantum Dots for Live Cells, in Vivo Imaging, and Diagnostics, Science, vol.307, issue.5709, pp.538-544, 2005.
DOI : 10.1126/science.1104274

B. Dubertret, In Vivo Imaging of Quantum Dots Encapsulated in Phospholipid Micelles, Science, vol.298, issue.5599, pp.1759-1762, 2002.
DOI : 10.1126/science.1077194

C. Murphy-royal, Surface diffusion of astrocytic glutamate transporters shapes synaptic transmission, Nature Neuroscience, vol.19, issue.2, pp.219-226, 2015.
DOI : 10.1038/368059a0
URL : https://hal.archives-ouvertes.fr/hal-01154386

E. A. Nance, A Dense Poly(Ethylene Glycol) Coating Improves Penetration of Large Polymeric Nanoparticles Within Brain Tissue, Science Translational Medicine, vol.4, issue.149, pp.149-119, 2012.
DOI : 10.1126/scitranslmed.3003594

R. G. Thorne and C. Nicholson, In vivo diffusion analysis with quantum dots and dextrans predicts the width of brain extracellular space, Proc. Natl Acad. Sci. USA 103, pp.5567-5572, 2006.
DOI : 10.1073/pnas.0509425103

A. Salvati, Transferrin-functionalized nanoparticles lose their targeting capabilities when a biomolecule corona adsorbs on the surface, Nature Nanotechnology, vol.100, issue.2, pp.137-143, 2013.
DOI : 10.1038/nnano.2012.237

M. Renner, Lateral Diffusion on Tubular Membranes: Quantification of Measurements Bias, PLoS ONE, vol.5, issue.9, p.25731, 2011.
DOI : 10.1371/journal.pone.0025731.s006

F. Gardoni and C. Bellone, Modulation of the glutamatergic transmission by Dopamine: a focus on Parkinson, Huntington and Addiction diseases, Frontiers in Cellular Neuroscience, vol.120, p.25, 2015.
DOI : 10.1016/s0306-4522(03)00326-9

D. L. Lodge and A. A. Grace, Hippocampal dysregulation of dopamine system function and the pathophysiology of schizophrenia, Trends in Pharmacological Sciences, vol.32, issue.9
DOI : 10.1016/j.tips.2011.05.001