The Scientific Discussion of Revealing Key Issue Aspects of Features of Simulation of Inflammatory Pain through AMPA Receptor Subunits of Exosome Origin
Keywords:
simulation, inflammatory, pain, AMPA receptor subunits, exosome origin
Abstract
The aim of the research was to study key issue aspects of features of simulation of inflammatory pain through AMPA receptor subunits of exosome origin in mice. The mechanism of functional modulation of AMPARs by their auxiliary subunits will benefit from further efforts to reach a tipping point where it will be useful for the development of improved therapies. Lipids require special attention because they may play an important role in the function of the AMPAR accessory subunit. Structural studies should only provide snapshots of complexes in action. Therefore, functional studies and molecular dynamics simulation approaches are expected to play an equally important role. Native AMPAR complexes contain more than one type of accessory subunits.
Downloads
How to Cite
References
A Kato, E Siuda, E Nisenbaum, D Bredt (2008) AMPA receptor subunit-specific regulation by a distinct family of type II TARPs. 59, 986-996.
Konstantin Khodosevich, Eric Jacobi, Paul Farrow, Anton Schulmann, Alexandru Rusu, Ling Zhang, Rolf Sprengel, Hannah Monyer, Jakob Von engelhardt (2014) Coexpressed Auxiliary Subunits Exhibit Distinct Modulatory Profiles on AMPA Receptor Function. 83(3), 601-615.
Anders Kielland, Paul Heggelund (2002) AMPA and NMDA currents show different short‐term depression in the dorsal lateral geniculate nucleus of the rat. 542(1), 99-106.
Eunjoon Kim, Morgan Sheng (2004) PDZ domain proteins of synapses. 5(10), 771-781.
R Klaassen, J Stroeder, F Coussen, A Hafner, J Petersen, C Renancio, L Schmitz, Normand Lodder, J Rotaru, D Rao-Ruiz, P Spijker, S Mansvelder, H Choquet, D Smit, A (2016) Shisa6 traps AMPA receptors at postsynaptic sites and prevents their desensitization during synaptic activity. 7, 10682.
Miloslav Korinek, Vojtech Vyklicky, Jirina Borovska, Katarina Lichnerova, Martina Kaniakova, Barbora Krausova, Jan Krusek, Ales Balik, Tereza Smejkalova, Martin Horak, Ladislav Vyklicky (2015) Cholesterol modulates open probability and desensitization of NMDA receptors. 593(10), 2279-2293.
Matthew Lee, Kevin Gardinier, Douglas Gernert, Douglas Schober, Rebecca Wright, He Wang, Yuewei Qian, Jeffrey Witkin, Eric Nisenbaum, Akihiko Kato (2017) Structural Determinants of the γ-8 TARP Dependent AMPA Receptor Antagonist. 8(12), 2631-2647.
E Lein, M Hawrylycz, N Ao, M Ayres, A Bensinger, A Bernard, A Boe, M Boguski, K Brockway, E Byrnes, L Chen, L Chen, T Chen, Chin Mc atlas of gene expression in the adult mouse brain. 445, 168-176.
Yu-Li Liu, Cathy Shen-Jang Fann, Chih-Min Liu, Wei Chen, Jer-Yuarn Wu, Shuen-Iu Hung, Chun-Houh Chen, Yuh-Shan Jou, Shi-Kai Liu, Tzung-Jeng Hwang, Ming Hsieh, Chien Chang, Wei-Chih Yang, Jin-Jia Lin, Frank Huang-Chih Chou, Stephen Faraone, Ming Tsuang, Hai-Gwo Hwu (2008) RASD2, MYH9, and CACNG2 Genes at Chromosome 22q12 Associated with the Subgroup of Schizophrenia with Non-Deficit in Sustained Attention and Executive Function. 64(9), 789-796.
S Long, X Tao, E Campbell, R Mackinnon (2007) Atomic structure of a voltage-dependent K+ channel in a lipid membrane-like environment. 450, 376-382.
Michael Maher, Jose Matta, Shenyan Gu, Mark Seierstad, David Bredt (2017) Getting a Handle on Neuropharmacology by Targeting Receptor-Associated Proteins. 96(5), 989-1001.
L Matt, L Kirk, G Chenaux, D Speca, K Puhger, M Pride, M Qneibi, T Haham, K Plambeck, Y Stern-Bach, J Silverman, J Crawley, J Hell, E Diaz (2018) SynDIG4/Prrt1 Is Required for Excitatory Synapse Development and Plasticity Underlying Cognitive Function. 22, 2246-2253.
L Mcgoldrick, A Singh, K Saotome, M Yelshanskaya, E Twomey, R Grassucci, A Sobolevsky (2018) Opening of the human epithelial calcium channel TRPV6. 553, 233-237.
Joel Meyerson, Janesh Kumar, Sagar Chittori, Prashant Rao, Jason Pierson, Alberto Bartesaghi, Mark Mayer, Sriram Subramaniam (2014) Structural mechanism of glutamate receptor activation and desensitization. 514(7522), 328-334.
A Milstein, R Nicoll (2009) TARP modulation of synaptic AMPA receptor trafficking and gating depends on multiple intracellular domains. 106, 11348-11351.
Aaron Milstein, Wei Zhou, Siavash Karimzadegan, David Bredt, Roger Nicoll (2007) TARP Subtypes Differentially and Dose-Dependently Control Synaptic AMPA Receptor Gating. 55(6), 905-918.
T Nakagawa (2010) The biochemistry, ultrastructure, and subunit assembly mechanism of AMPA receptors. 42, 161-184.
L Cai, G Courtine, A Fong, J Burdick, R Roy, V Edgerton (2006) Plasticity of functional connectivity in the adult spinal cord. 361, 1635-1646.
A Craig (2003) PAIN MECHANISMS: Labeled Lines Versus Convergence in Central Processing. 26(1), 1-30.
Holly Engelman, Amy Macdermott (2004) Presynaptic ionotropic receptors and control of transmitter release. 5(2), 135-145.
E Fetz, S Perlmutter, Y Prut, K Seki, S Votaw (2002) Roles of primate spinal interneurons in preparation and execution of voluntary hand movement. 40(1-3), 53-65.
Amy Helms, Jane Johnson (2003) Specification of dorsal spinal cord interneurons. 13(1), 42-49.
Barry Jacobs, Casimir Fornal (1993) 5-HT and motor control: a hypothesis. 16(9), 346-352.
E Jankowska (1992) Interneuronal relay in spinal pathways from proprioceptors. 38, 335-378.
R Ji, T Kohno, K Moore, C Woolf (2003) Central sensitization and LTP: do pain and memory share similar mechanisms?. 26, 696-705.
Ole Kiehn (2006) LOCOMOTOR CIRCUITS IN THE MAMMALIAN SPINAL CORD. 29(1), 279-306.
Soo-Kyung Lee, Samuel Pfaff (2001) Transcriptional networks regulating neuronal identity in the developing spinal cord. 4(S11), 1183-1191.
David Mclean, Jingyi Fan, Shin-Ichi Higashijima, Melina Hale, Joseph Fetcho (2007) A topographic map of recruitment in spinal cord. 446(7131), 71-75.
Mark Millan (2002) Descending control of pain. 66(6), 355-474.
Richard Poppele, Gianfranco Bosco (2003) Sophisticated spinal contributions to motor control. 26(5), 269-276.
Serge Rossignol, Réjean Dubuc, Jean-Pierre Gossard (2006) Dynamic Sensorimotor Interactions in Locomotion. 86(1), 89-154.
P Rudomin, Robert Schmidt (1999) Presynaptic inhibition in the vertebrate spinal cord revisited. 129(1), 1-37.
K Seki, S Perlmutter, E Fetz (2003) Sensory input to primate spinal cord is presynaptically inhibited during voluntary movement. 6, 1309-1316.
W Willis, R Coggeshall (1991) Sensory Mechanisms of the Spinal Cord, Second Edition.
Ingo Greger, Jake Watson, Stuart Cull-Candy (2017) Structural and Functional Architecture of AMPA-Type Glutamate Receptors and Their Auxiliary Proteins. 94(4), 713-730.
Philip Chang, David Verbich, R Mckinney (2012) AMPA receptors as drug targets in neurological disease - advantages, caveats, and future outlook. 35(12), 1908-1916.
C Chen, D Blitz, Wg (2002) Contributions of receptor desensitization and saturation to plasticity at the retinogeniculate synapse. 33, 779-788.
C Chen, W Regehr (2000) Developmental remodeling of the retinogeniculate synapse. 28, 955-966.
Lu Chen, Dane Chetkovich, Ronald Petralia, Neal Sweeney, Yoshimi Kawasaki, Robert Wenthold, David Bredt, Roger Nicoll (2000) Stargazin regulates synaptic targeting of AMPA receptors by two distinct mechanisms. 408(6815), 936-943.
Lei Chen, Katharina Dürr, Eric Gouaux (2014) X-ray structures of AMPA receptor-cone snail toxin complexes illuminate activation mechanism. 345(6200), 1021-1026.
Shanshuang Chen, Eric Gouaux (2019) Structure and mechanism of AMPA receptor - auxiliary protein complexes. 54, 104-111.
S Chen, Y Zhao, Y Wang, M Shekhar, E Tajkhorshid, E (2017) Activation and Desensitization Mechanism of AMPA Receptor-TARP Complex by Cryo-EM. 170, 1234-1246.
Xufeng Chen, Muhammad Aslam, Tim Gollisch, Kevin Allen, Jakob Von Engelhardt (2018) CKAMP44 modulates integration of visual inputs in the lateral geniculate nucleus. 9(1), 261.
Tomohiro Chiyonobu, Shin Hayashi, Kazuhiro Kobayashi, Masafumi Morimoto, Yuri Miyanomae, Akira Nishimura, Akemi Nishimoto, Chiyomi Ito, Issei Imoto, Tohru Sugimoto, Zhengping Jia, Johji Inazawa, Tatsushi Toda (2007) Partial tandem duplication of GRIA3 in a male with mental retardation. 143A(13), 1448-1455.
Chang-Hoon Cho, Fannie St-Gelais, Wei Zhang, Susumu Tomita, James Howe (2007) Two Families of TARP Isoforms that Have Distinct Effects on the Kinetic Properties of AMPA Receptors and Synaptic Currents. 55(6), 890-904.
Graham Collingridge, Richard Olsen, John Peters, Michael Spedding (2009) A nomenclature for ligand-gated ion channels. 56(1), 2-5.
I Coombs, D Soto, M Zonouzi, M Renzi, C Shelley, M Farrant, S Cull-Candy (2012) Cornichons Modify Channel Properties of Recombinant and Glial AMPA Receptors. 32(29), 9796-9804.
B Davies, L Brown, O Cais, J Watson, A Clayton, V Chang, D Biggs, C Preece, P Hernandez-Pliego, J Krohn, A Bhomra, Srf Twigg, A Rimmer, A Kanapin, Wgs Consortium, A Sen, Z Zaiwalla, G Mcvean, R Foster, P Donnelly, J Taylor, E Blair, D Nutt, A Aricescu, I Greger, S Peirson, J & Flint, H Martin (2017) A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability. 26, 3869-3882.
G Dawe, Md. Kadir, Raminta Venskutonytė, Amanda Perozzo, Yuhao Yan, Ryan Alexander, Camilo Navarrete, Eduardo Santander, Marika Arsenault, Christian Fuentes, Mark Aurousseau, Karla Frydenvang, Nelson Barrera, Jette Kastrup, J Edwardson, Derek Bowie (2019) Nanoscale Mobility of the Apo State and TARP Stoichiometry Dictate the Gating Behavior of Alternatively Spliced AMPA Receptors. 102(5), 976-992.e5.
G Dawe, M Musgaard, M Aurousseau, N Nayeem, T Green, P Biggin, D Bowie (2016) Distinct Structural Pathways Coordinate the Activation of AMPA Receptor-Auxiliary Subunit Complexes. 89, 1264-1276.
Javier Díaz-Alonso, Yujiao Sun, Adam Granger, Jonathan Levy, Sabine Blankenship, Roger Nicoll (2017) Subunit-specific role for the amino-terminal domain of AMPA receptors in synaptic targeting. 114(27), 7136-7141.
K Durr, L Chen, R Stein, De Zorzi, R Folea, I Walz, T Mchaourab, H, E (2014) Structure and Dynamics of AMPA Receptor GluA2 in Resting, Pre-Open, and Desensitized States. 158, 778-792.
Nadine Erlenhardt, Hong Yu, Kavitha Abiraman, Tokiwa Yamasaki, Jacques Wadiche, Susumu Tomita, David Bredt (2016) Porcupine Controls Hippocampal AMPAR Levels, Composition, and Synaptic Transmission. 14(4), 782-794.
Kate Everett, Barry Chioza, Jean Aicardi, Harald Aschauer, Oebele Brouwer, Petra Callenbach, Athanasios Covanis, Olivier Dulac, Orvar Eeg-Olofsson, Martha Feucht, Mogens Friis, Françoise Goutieres, Renzo Guerrini, Armin Heils, Marianne Kjeldsen, Anna-Elina Lehesjoki, Andrew Makoff, Rima Nabbout, Ingrid Olsson, Thomas Sander, Auli Sirén, Paul Mckeigue, Robert Robinson, Nichole Taske, Michele Rees, Mark Gardiner (2007) Linkage and association analysis of CACNG3 in childhood absence epilepsy. 15(4), 463-472.
Karijn Floor, Tuva Barøy, Doriana Misceo, Øivind Kanavin, Madeleine Fannemel, Eirik Frengen (2012) A 1 Mb de novo deletion within 11q13.1q13.2 in a boy with mild intellectual disability and minor dysmorphic features. 55(12), 695-699.
Masahiro Fukaya, Maya Yamazaki, Kenji Sakimura, Masahiko Watanabe (2005) Spatial diversity in gene expression for VDCCγ subunit family in developing and adult mouse brains. 53(4), 376-383.
J Garcia-Nafria, B Herguedas, J Watson, Ih (2016) The dynamic AMPA receptor extracellular region: a platform for synaptic protein interactions. 594, 5449-5458.
K Gardinier, D Gernert, W Porter, J Reel, P Ornstein, P Spinazze, F Stevens, P Hahn, S Hollinshead, D Mayhugh, J Schkeryantz, A Khilevich, O De Frutos, S Gleason, A Kato, D Luffer-Atlas, P Desai, S Swanson, K Burris, C Ding, B Heinz, A Need, V Barth, G Stephenson, B Diseroad, T Woods, H Yu, D Bredt, J Witkin (2016) Discovery of the First alpha-Amino-3hydroxy-5-methyl-4-isoxazolepropionic Acid (AMPA) Receptor Antagonist Dependent upon Transmembrane AMPA Receptor Regulatory Protein (TARP) gamma-8. 59, 4753-4768.
Martin Gill, Akihiko Kato, Matthew Roberts, Hong Yu, He Wang, Susumu Tomita, David Bredt (2011) Cornichon-2 Modulates AMPA Receptor-Transmembrane AMPA Receptor Regulatory Protein Assembly to Dictate Gating and Pharmacology. 31(18), 6928-6938.
Xinglong Gu, Xia Mao, Marc Lussier, Mary Hutchison, Liang Zhou, F Hamra, Katherine Roche, Wei Lu (2016) GSG1L suppresses AMPA receptor-mediated synaptic transmission and uniquely modulates AMPA receptor kinetics in hippocampal neurons. 7(1), 10873.
Karl Hackmann, Sarah Matko, Eva-Maria Gerlach, Maja Von Der Hagen, Barbara Klink, Evelin Schrock, Andreas Rump, Nataliya Di Donato (2013) Partial deletion of GLRB and GRIA2 in a patient with intellectual disability. 21(1), 112-114.
Fadi Hamdan, Julie Gauthier, Yoichi Araki, Da-Ting Lin, Yuhki Yoshizawa, Kyohei Higashi, A Park, Dan Spiegelman, Sylvia Dobrzeniecka, Amélie Piton, Hideyuki Tomitori, Hussein Daoud, Christine Massicotte, Edouard Henrion, Ousmane Diallo, Masoud Shekarabi, Claude Marineau, Michael Shevell, Bruno Maranda, Grant Mitchell, Amélie Nadeau, Guy D'anjou, Michel Vanasse, Myriam Srour, Ronald Lafrenière, Pierre Drapeau, Jean Lacaille, Eunjoon Kim, Jae-Ran Lee, Kazuei Igarashi, Richard Huganir, Guy Rouleau, Jacques Michaud (2011) Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual Disability. 88(3), 306-316.
Wenyan Han, Jun Li, Kenneth Pelkey, Saurabh Pandey, Xiumin Chen, Ya-Xian Wang, Kunwei Wu, Lihao Ge, Tianming Li, David Castellano, Chengyu Liu, Ling-Gang Wu, Ronald Petralia, Joseph Lynch, Chris Mcbain, Wei Lu (2019) Shisa7 is a GABA A receptor auxiliary subunit controlling benzodiazepine actions. 366(6462), 246-250.
Kasper Hansen, Hiro Furukawa, Stephen Traynelis (2010) Control of Assembly and Function of Glutamate Receptors by the Amino-Terminal Domain. 78(4), 535-549.
Natalie Hawken, Elena Zaika, Terunaga Nakagawa (2017) Engineering defined membrane‐embedded elements of AMPA receptor induces opposing gating modulation by cornichon 3 and stargazin. 595(20), 6517-6539.
Beatriz Herguedas, Javier García-Nafría, Ondrej Cais, Rafael Fernández-Leiro, James Krieger, Hinze Ho, Ingo Greger (2016) Structure and organization of heteromeric AMPA-type glutamate receptors. 352(6285), 3873.
Beatriz Herguedas, Jake Watson, Hinze Ho, Ondrej Cais, Javier García-Nafría, Ingo Greger (2019) Architecture of the heteromeric GluA1/2 AMPA receptor in complex with the auxiliary subunit TARP γ8. 364(6438).
H Hering, C Lin, M Sheng (2003) Lipid rafts in the maintenance of synapses, dendritic spines, and surface AMPA receptor stability. 23, 3262-3271.
Bruce Herring, Yun Shi, Young Suh, Chan-Ying Zheng, Sabine Blankenship, Katherine Roche, Roger Nicoll (2013) Cornichon Proteins Determine the Subunit Composition of Synaptic AMPA Receptors. 77(6), 1083-1096.
Michael Hollmann, Cornelia Maron, Stephen Heinemann (1994) N-glycosylation site tagging suggests a three transmembrane domain topology for the glutamate receptor GluR1. 13(6), 1331-1343.
H Hoshino, T Uchida, T Otsuki, S Kawamoto, K Okubo, M Takeichi, O Chisaka (2007) Cornichon-like protein facilitates secretion of HB-EGF and regulates proper development of cranial nerves. 18, 1143-1152.
Richard Huganir, Roger Nicoll (2013) AMPARs and Synaptic Plasticity: The Last 25 Years. 80(3), 704-717.
Johansen Amin, Catherine Salussolia, Kelvin Chan, Michael Regan, Jian Dai, Huan-Xiang Zhou, Hiro Furukawa, Mark Bowen, Lonnie Wollmuth (2017) Divergent roles of a peripheral transmembrane segment in AMPA and NMDA receptors. 149(6), 661-680.
Armstrong N & Gouaux, E (2000) Mechanisms for activation and antagonism of an AMPA-sensitive glutamate receptor: crystal structures of the GluR2 ligand binding core. 28, 165-181.
Neali Armstrong, Yu Sun, Guo-Qiang Chen, Eric Gouaux (1998) Structure of a glutamate-receptor ligand-binding core in complex with kainate. 395(6705), 913-917.
Gai Ayalon, Yael Stern-Bach (2001) Functional Assembly of AMPA and Kainate Receptors Is Mediated by Several Discrete Protein-Protein Interactions. 31(1), 103-113.
Caleigh Azumaya, Emily Days, Paige Vinson, Shaun Stauffer, Gary Sulikowski, C Weaver, Terunaga Nakagawa (2017) Screening for AMPA receptor auxiliary subunit specific modulators. 12(3), e0174742.
A Ben-Yaacov, M Gillor, T Haham, A Parsai, M Qneibi, Y Stern-Bach (2017) Molecular Mechanism of AMPA Receptor Modulation by TARP/Stargazin.
Craig Blackstone, Stephen Moss, Lee Martin, Allan Levey, Donald Price, Richard Huganir (2002) Biochemical Characterization and Localization of a Non‐N‐Methyl‐D‐Aspartate Glutamate Receptor in Rat Brain. 58(3), 1118-1126.
C Bonnet, B Leheup, M Béri, C Philippe, M Grégoire, P Jonveaux (2009) Aberrant GRIA3 transcripts with multi‐exon duplications in a family with X‐linked mental retardation. 149A(6), 1280-1289.
S Boudkkazi, A Brechet, J Schwenk, B (2014) Cornichon2 dictates the time course of excitatory transmission at individual hippocampal synapses. 82, 848-858.
Penelope Brockie, Michael Jensen, Jerry Mellem, Erica Jensen, Tokiwa Yamasaki, Rui Wang, Dane Maxfield, Colin Thacker, Frédéric Hoerndli, Patrick Dunn, Susumu Tomita, David Madsen, Andres Maricq (2013) Cornichons Control ER Export of AMPA Receptors to Regulate Synaptic Excitability. 80(1), 129-142.
Patricia Brown, Hugo Mcguire, Derek Bowie (2018) Stargazin and cornichon-3 relieve polyamine block of AMPA receptors by enhancing blocker permeation. 150(1), 67-82.
Ananth Burada, Rajesh Vinnakota, Janesh Kumar (2020) Cryo-EM structures of the ionotropic glutamate receptor GluD1 reveal a non-swapped architecture. 27(1), 84-91.
Ondrej Cais, Beatriz Herguedas, Karolina Krol, Stuart Cull-Candy, Mark Farrant, Ingo Greger (2014) Mapping the Interaction Sites between AMPA Receptors and TARPs Reveals a Role for the Receptor N-Terminal Domain in Channel Gating. 9(2), 728-740.
Elisa Carrillo, Sana Shaikh, Vladimir Berka, Ryan Durham, Douglas Litwin, Garam Lee, David Maclean, Linda Nowak, Vasanthi Jayaraman (2020) Mechanism of modulation of AMPA receptors by TARP-γ8. 152(1).
C Chen, D Blitz, W Regehr (2002) Contributions of receptor desensitization and saturation to plasticity at the retinogeniculate synapse. 33, 779-788.
Chinfei Chen, Wade Regehr (2000) Developmental Remodeling of the Retinogeniculate Synapse. 28(3), 955-966.
L Chen, K Durr, E Gouaux (2014) X-ray structures of AMPA receptor-cone snail toxin complexes illuminate activation mechanism. 345, 1021-1026.
S Chen, Y Zhao, Y Wang, M Shekhar, E Tajkhorshid, E Gouaux (2017) Activation and Desensitization Mechanism of AMPA Receptor-TARP Complex by Cryo-EM. 170, 1234-1246.
I Coombs, D Soto, M Zonouzi, M Renzi, C Shelley, M Farrant, S Cull-Candy (2012) Cornichons modify channel properties of recombinant and glial AMPA receptors. 32, 9796-9804.
Benjamin Davies, Laurence Brown, Ondrej Cais, Jake Watson, Amber Clayton, Veronica Chang, Daniel Biggs, Christopher Preece, Polinka Hernandez-Pliego, Jon Krohn, Amarjit Bhomra, Stephen Twigg, Andrew Rimmer, Alexander Kanapin, Arjune Sen, Zenobia Zaiwalla, Gil Mcvean, Russell Foster, Peter Donnelly, Jenny Taylor, Edward Blair, David Nutt, A Aricescu, Ingo Greger, Stuart Peirson, Jonathan Flint, Hilary Martin (2017) A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability. 26(20), 3869-3882.
G Dawe, M Kadir, R Venskutonyte, A Perozzo, Y Yan, Rpd Alexander, C Navarrete, E Santander, M Arsenault, C Fuentes, Mrp Aurousseau, K Frydenvang, N Barrera, J Kastrup, J Edwardson, D ; Bowie, G Dawe, M Musgaard, M Aurousseau, N Nayeem, T Green, P Biggin, D ; Bowie, S ; Hochman, Mb, A Kato, M Roberts, H Yu, H Wang, S Tomita, Ds ; &bredt, I Greger, J Watson, S Cull-Candy (2007) Nanoscale Mobility of the Apo State and TARP Stoichiometry Dictate the Gating Behavior of Alternatively Spliced AMPA Receptors. 102(22), 105.
X Gu, X Mao, M Lussier, M Hutchison, L Zhou, F Hamra, K Roche, W Lu (2016) GSG1L suppresses AMPA receptor-mediated synaptic transmission and uniquely modulates AMPA receptor kinetics in hippocampal neurons. 7, 106.
K Hackmann, S Matko, E Gerlach, Von Der Hagen, M Klink, B Schrock, E Rump, A, Di Donato, N ; Gauthier, J Araki, Y Lin, D Yoshizawa, Y Higashi, K Park, A Spiegelman, D Dobrzeniecka, S Piton, A Tomitori, H Daoud, H Massicotte, C Henrion, E Diallo, O Group, S Shekarabi, M Marineau, C Shevell, M, Maranda Mitchell, G Nadeau, A, D 'anjou, G Vanasse, M Srour, M Lafreniere, R Drapeau, P Lacaille, J Kim, E Lee, J Igarashi, K Huganir, R Rouleau, G Michaud, J (2011) Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability. 21, 108.
Wenyan Han, Jun Li, Kenneth Pelkey, Saurabh Pandey, Xiumin Chen, Ya-Xian Wang, Kunwei Wu, Lihao Ge, Tianming Li, David Castellano, Chengyu Liu, Ling-Gang Wu, Ronald Petralia, Joseph Lynch, Chris Mcbain, Wei Lu (2010) Shisa7 is a GABA A receptor auxiliary subunit controlling benzodiazepine actions. 366(6462), 246-250.
Beatriz Herguedas, Javier García-Nafría, Ondrej Cais, Rafael Fernández-Leiro, James Krieger, Hinze Ho, Ingo Greger (2016) Structure and organization of heteromeric AMPA-type glutamate receptors. 352(6285), 3873-3112.
Beatriz Herguedas, Jake Watson, Hinze Ho, Ondrej Cais, Javier García-Nafría, Ingo Greger (2019) Architecture of the heteromeric GluA1/2 AMPA receptor in complex with the auxiliary subunit TARP γ8. 364(6438), 113.
Heike Hering, Chih-Chun Lin, Morgan Sheng (2003) Lipid Rafts in the Maintenance of Synapses, Dendritic Spines, and Surface AMPA Receptor Stability. 23(8), 3262-3271.
M Hollmann, C Maron, S ; Heinemann, H Hoshino, T Uchida, T Otsuki, S Kawamoto, K Okubo, M Takeichi, O Chisaka (1994) Nglycosylation site tagging suggests a three transmembrane domain topology for the glutamate receptor GluR1. 13, 117.
A Jackson, R Nicoll (2011) The expanding social network of ionotropic glutamate receptors: TARPs and other transmembrane auxiliary subunits. 70, 119.
Rongsheng Jin, Satinder Singh, Shenyan Gu, Hiroyasu Furukawa, Alexander Sobolevsky, Jie Zhou, Yan Jin, Eric Gouaux (2009) Crystal structure and association behaviour of the GluR2 amino‐terminal domain. 28(12), 1812-1823.
Evgenia Kalashnikova, Ramón Lorca, Inderpreet Kaur, Gustavo Barisone, Bonnie Li, Tatsuto Ishimaru, James Trimmer, Durga Mohapatra, Elva Díaz (2010) SynDIG1: An Activity-Regulated, AMPA- Receptor-Interacting Transmembrane Protein that Regulates Excitatory Synapse Development. 65(1), 80-93.
M Kang, M Nuriya, Y Guo, K Martindale, D Lee, Rl ; Kato, A Burris, K Gardinier, K Gernert, D Porter, W Reel, J Ding, C Tu, Y Schober, D Lee, M Heinz, B Fitch, T Gleason, S Catlow, J Yu, H Fitzjohn, S Pasqui, F Wang, H Qian, Y Sher, E Zwart, R Wafford, K Rasmussen, K Ornstein, P Isaac, J Nisenbaum, E Bredt, D Witkin, J Kamalova, A Nakagawa, T ; Kato, A Gill, M Ho, M Yu, H Tu, Y Siuda, E Wang, H Qian, Y Nisenbaum, E Tomita, S Ds (2010) Forebrain-selective AMPA-receptor antagonism guided by TARP gamma-8 as an antiepileptic mechanism. 22(2), 125.
Alexander Jackson, Roger Nicoll (2011) The Expanding Social Network of Ionotropic Glutamate Receptors: TARPs and Other Transmembrane Auxiliary Subunits. 70(2), 178-199.
Jason Shepherd, Richard Huganir (2007) The Cell Biology of Synaptic Plasticity: AMPA Receptor Trafficking. 23(1), 613-643.
Published
2024-12-07
Issue
Section
License
Copyright (c) 2024 Authors and Global Journals Private Limited

This work is licensed under a Creative Commons Attribution 4.0 International License.