Cited by 152Neuroscience and Neuropharmacology ResearchNeural dynamics and brain functionMemory and Neural Mechanisms

The interplay between Hebbian and homeostatic synaptic plasticity

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Vitureira, Nathalia, Goda, Yukiko·2013·Journal of Cell Biology

Abstract

Synaptic plasticity, a change in the efficacy of synaptic signaling, is a key property of synaptic communication that is vital to many brain functions. Hebbian forms of long-lasting synaptic plasticity—long-term potentiation (LTP) and long-term depression (LTD)—have been well studied and are considered to be the cellular basis for particular types of memory. Recently, homeostatic synaptic plasticity, a compensatory form of synaptic strength change, has attracted attention as a cellular mechanism that counteracts changes brought about by LTP and LTD to help stabilize neuronal network activity. New findings on the cellular mechanisms and molecular players of the two forms of plasticity are uncovering the interplay between them in individual neurons.

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  1. Abbott L.F. Regehr W.G. 2004 Synaptic computation. Nature. 431: 796– 803 10.1038/nature03010 15483601 · DOI · Paper page
  2. Alvarez V.A. Sabatini B.L. 2007 Anatomical and physiological plasticity of dendritic spines. Annu. Rev. Neurosci. 30: 79– 97 10.1146/annurev.neuro.30.051606.094222 17280523 · DOI · Paper page
  3. Andersen P. Sundberg S.H. Sveen O. Wigström H. 1977 Specific long-lasting potentiation of synaptic transmission in hippocampal slices. Nature. 266: 736– 737 10.1038/266736a0 195210 · DOI
  4. Arendt K.L. Sarti F. Chen L. 2013 Chronic inactivation of a neural circuit enhances LTP by inducing silent synapse formation. J. Neurosci. 33: 2087– 2096 10.1523/JNEUROSCI.3880-12.2013 23365245 PMC3804283 · DOI
  5. Bacci A. Coco S. Pravettoni E. Schenk U. Armano S. Frassoni C. Verderio C. De Camilli P. Matteoli M. 2001 Chronic blockade of glutamate receptors enhances presynaptic release and downregulates the interaction between synaptophysin-synaptobrevin-vesicle-associated membrane protein 2. J. Neurosci. 21: 6588– 6596 11517248 PMC6763110
  6. Bannai H. Lévi S. Schweizer C. Inoue T. Launey T. Racine V. Sibarita J.B. Mikoshiba K. Triller A. 2009 Activity-dependent tuning of inhibitory neurotransmission based on GABAAR diffusion dynamics. Neuron. 62: 670– 682 10.1016/j.neuron.2009.04.023 19524526 · DOI
  7. Bats C. Groc L. Choquet D. 2007 The interaction between Stargazin and PSD-95 regulates AMPA receptor surface trafficking. Neuron. 53: 719– 734 10.1016/j.neuron.2007.01.030 17329211 · DOI · Paper page
  8. Bi G. Poo M. 2001 Synaptic modification by correlated activity: Hebb’s postulate revisited. Annu. Rev. Neurosci. 24: 139– 166 10.1146/annurev.neuro.24.1.139 11283308 · DOI
  9. Bliss T.V. Collingridge G.L. 1993 A synaptic model of memory: long-term potentiation in the hippocampus. Nature. 361: 31– 39 10.1038/361031a0 8421494 · DOI · Paper page
  10. Bliss T.V. Lomo T. 1973 Long-lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path. J. Physiol. 232: 331– 356 4727084 PMC1350458
  11. Blundell J. Blaiss C.A. Etherton M.R. Espinosa F. Tabuchi K. Walz C. Bolliger M.F. Südhof T.C. Powell C.M. 2010 Neuroligin-1 deletion results in impaired spatial memory and increased repetitive behavior. J. Neurosci. 30: 2115– 2129 10.1523/JNEUROSCI.4517-09.2010 20147539 PMC2824441 · DOI · Paper page
  12. Bortolotto Z.A. Nistico R. More J.C. Jane D.E. Collingridge G.L. 2005 Kainate receptors and mossy fiber LTP. Neurotoxicology. 26: 769– 777 10.1016/j.neuro.2005.02.004 15939476 · DOI
  13. Bozdagi O. Shan W. Tanaka H. Benson D.L. Huntley G.W. 2000 Increasing numbers of synaptic puncta during late-phase LTP: N-cadherin is synthesized, recruited to synaptic sites, and required for potentiation. Neuron. 28: 245– 259 10.1016/S0896-6273(00)00100-8 11086998 · DOI
  14. Bozdagi O. Wang X.B. Nikitczuk J.S. Anderson T.R. Bloss E.B. Radice G.L. Zhou Q. Benson D.L. Huntley G.W. 2010 Persistence of coordinated LTP and dendritic spine enlargement at mature hippocampal CA1 synapses requires N-cadherin. J. Neurosci. 30: 9984– 9989 10.1523/JNEUROSCI.1223-10.2010 20668183 PMC2921177 · DOI · Paper page
  15. Brigidi G.S. Bamji S.X. 2011 Cadherin-catenin adhesion complexes at the synapse. Curr. Opin. Neurobiol. 21: 208– 214 10.1016/j.conb.2010.12.004 21255999 · DOI
  16. Burrone J. O’Byrne M. Murthy V.N. 2002 Multiple forms of synaptic plasticity triggered by selective suppression of activity in individual neurons. Nature. 420: 414– 418 10.1038/nature01242 12459783 · DOI · Paper page
  17. Cajigas I.J. Will T. Schuman E.M. 2010 Protein homeostasis and synaptic plasticity. EMBO J. 29: 2746– 2752 10.1038/emboj.2010.173 20717144 PMC2924649 · DOI
  18. Castillo P.E. Janz R. Südhof T.C. Tzounopoulos T. Malenka R.C. Nicoll R.A. 1997 Rab3A is essential for mossy fibre long-term potentiation in the hippocampus. Nature. 388: 590– 593 10.1038/41574 9252190 · DOI · Paper page
  19. Castillo P.E. Schoch S. Schmitz F. Südhof T.C. Malenka R.C. 2002 RIM1alpha is required for presynaptic long-term potentiation. Nature. 415: 327– 330 10.1038/415327a 11797010 · DOI · Paper page
  20. Cingolani L.A. Goda Y. 2008 Actin in action: the interplay between the actin cytoskeleton and synaptic efficacy. Nat. Rev. Neurosci. 9: 344– 356 10.1038/nrn2373 18425089 · DOI · Paper page
  21. Colledge M. Dean R.A. Scott G.K. Langeberg L.K. Huganir R.L. Scott J.D. 2000 Targeting of PKA to glutamate receptors through a MAGUK-AKAP complex. Neuron. 27: 107– 119 10.1016/S0896-6273(00)00013-1 10939335 · DOI · Paper page
  22. Dani A. Huang B. Bergan J. Dulac C. Zhuang X. 2010 Superresolution imaging of chemical synapses in the brain. Neuron. 68: 843– 856 10.1016/j.neuron.2010.11.021 21144999 PMC3057101 · DOI
  23. Del Castillo J. Katz B. 1954 Quantal components of the end-plate potential. J. Physiol. 124: 560– 573 13175199 PMC1366292
  24. Dityatev A. Schachner M. Sonderegger P. 2010 The dual role of the extracellular matrix in synaptic plasticity and homeostasis. Nat. Rev. Neurosci. 11: 735– 746 10.1038/nrn2898 20944663 · DOI · Paper page
  25. Echegoyen J. Neu A. Graber K.D. Soltesz I. 2007 Homeostatic plasticity studied using in vivo hippocampal activity-blockade: synaptic scaling, intrinsic plasticity and age-dependence. PLoS ONE. 2: e700 10.1371/journal.pone.0000700 17684547 PMC1933594 · DOI · Paper page
  26. Ehlers M.D. Heine M. Groc L. Lee M.C. Choquet D. 2007 Diffusional trapping of GluR1 AMPA receptors by input-specific synaptic activity. Neuron. 54: 447– 460 10.1016/j.neuron.2007.04.010 17481397 PMC1993808 · DOI · Paper page
  27. Ehrlich I. Klein M. Rumpel S. Malinow R. 2007 PSD-95 is required for activity-driven synapse stabilization. Proc. Natl. Acad. Sci. USA. 104: 4176– 4181 10.1073/pnas.0609307104 17360496 PMC1820728 · DOI · Paper page
  28. Fisher-Lavie A. Ziv N.E. 2013 Matching dynamics of presynaptic and postsynaptic scaffolds. J. Neurosci. 33: 13094– 13100 10.1523/JNEUROSCI.2144-13.2013 23926263 PMC6619726 · DOI
  29. Fourcaudot E. Gambino F. Humeau Y. Casassus G. Shaban H. Poulain B. Lüthi A. 2008 cAMP/PKA signaling and RIM1alpha mediate presynaptic LTP in the lateral amygdala. Proc. Natl. Acad. Sci. USA. 105: 15130– 15135 10.1073/pnas.0806938105 18815362 PMC2567504 · DOI · Paper page
  30. Frischknecht R. Gundelfinger E.D. 2012 The brain’s extracellular matrix and its role in synaptic plasticity. Adv. Exp. Med. Biol. 970: 153– 171 10.1007/978-3-7091-0932-8_7 22351055 · DOI · Paper page
  31. Futai K. Kim M.J. Hashikawa T. Scheiffele P. Sheng M. Hayashi Y. 2007 Retrograde modulation of presynaptic release probability through signaling mediated by PSD-95-neuroligin. Nat. Neurosci. 10: 186– 195 10.1038/nn1837 17237775 PMC4755312 · DOI
  32. Graf E.R. Valakh V. Wright C.M. Wu C. Liu Z. Zhang Y.Q. DiAntonio A. 2012 RIM promotes calcium channel accumulation at active zones of the Drosophila neuromuscular junction. J. Neurosci. 32: 16586– 16596 10.1523/JNEUROSCI.0965-12.2012 23175814 PMC3516196 · DOI
  33. Granger A.J. Shi Y. Lu W. Cerpas M. Nicoll R.A. 2013 LTP requires a reserve pool of glutamate receptors independent of subunit type. Nature. 493: 495– 500 10.1038/nature11775 23235828 PMC3998843 · DOI · Paper page
  34. Han Y. Kaeser P.S. Südhof T.C. Schneggenburger R. 2011 RIM determines Ca²+ channel density and vesicle docking at the presynaptic active zone. Neuron. 69: 304– 316 10.1016/j.neuron.2010.12.014 21262468 PMC3259453 · DOI · Paper page
  35. Heine M. Groc L. Frischknecht R. Béïque J.C. Lounis B. Rumbaugh G. Huganir R.L. Cognet L. Choquet D. 2008 Surface mobility of postsynaptic AMPARs tunes synaptic transmission. Science. 320: 201– 205 10.1126/science.1152089 18403705 PMC2715948 · DOI · Paper page
  36. Holt M. Varoqueaux F. Wiederhold K. Takamori S. Urlaub H. Fasshauer D. Jahn R. 2006 Identification of SNAP-47, a novel Qbc-SNARE with ubiquitous expression. J. Biol. Chem. 281: 17076– 17083 10.1074/jbc.M513838200 16621800 · DOI
  37. Huang G.Z. Ujihara H. Takahashi S. Kaba H. Yagi T. Inoue S. 2000 Involvement of complexin II in synaptic plasticity in the CA1 region of the hippocampus: the use of complexin II-lacking mice. Jpn. J. Pharmacol. 84: 179– 187 10.1254/jjp.84.179 11128041 · DOI
  38. Huang Y.Y. Zakharenko S.S. Schoch S. Kaeser P.S. Janz R. Südhof T.C. Siegelbaum S.A. Kandel E.R. 2005 Genetic evidence for a protein-kinase-A-mediated presynaptic component in NMDA-receptor-dependent forms of long-term synaptic potentiation. Proc. Natl. Acad. Sci. USA. 102: 9365– 9370 10.1073/pnas.0503777102 15967982 PMC1166627 · DOI · Paper page
  39. Inoue A. Okabe S. 2003 The dynamic organization of postsynaptic proteins: translocating molecules regulate synaptic function. Curr. Opin. Neurobiol. 13: 332– 340 10.1016/S0959-4388(03)00077-1 12850218 · DOI
  40. Jakawich S.K. Nasser H.B. Strong M.J. McCartney A.J. Perez A.S. Rakesh N. Carruthers C.J. Sutton M.A. 2010 Local presynaptic activity gates homeostatic changes in presynaptic function driven by dendritic BDNF synthesis. Neuron. 68: 1143– 1158 10.1016/j.neuron.2010.11.034 21172615 PMC3046391 · DOI · Paper page
  41. Jurado S. Goswami D. Zhang Y. Molina A.J. Südhof T.C. Malenka R.C. 2013 LTP requires a unique postsynaptic SNARE fusion machinery. Neuron. 77: 542– 558 10.1016/j.neuron.2012.11.029 23395379 PMC3569727 · DOI · Paper page
  42. Kay L. Humphreys L. Eickholt B.J. Burrone J. 2011 Neuronal activity drives matching of pre- and postsynaptic function during synapse maturation. Nat. Neurosci. 14: 688– 690 10.1038/nn.2826 21532580 · DOI · Paper page
  43. Kennedy M.J. Davison I.G. Robinson C.G. Ehlers M.D. 2010 Syntaxin-4 defines a domain for activity-dependent exocytosis in dendritic spines. Cell. 141: 524– 535 10.1016/j.cell.2010.02.042 20434989 PMC2874581 · DOI · Paper page
  44. Kwon H.B. Kozorovitskiy Y. Oh W.J. Peixoto R.T. Akhtar N. Saulnier J.L. Gu C. Sabatini B.L. 2012 Neuroligin-1-dependent competition regulates cortical synaptogenesis and synapse number. Nat. Neurosci. 15: 1667– 1674 10.1038/nn.3256 23143522 PMC3536444 · DOI
  45. Lawrence J.J. McBain C.J. 2003 Interneuron diversity series: containing the detonation—feedforward inhibition in the CA3 hippocampus. Trends Neurosci. 26: 631– 640 10.1016/j.tins.2003.09.007 14585604 · DOI · Paper page
  46. Lazarevic V. Schöne C. Heine M. Gundelfinger E.D. Fejtova A. 2011 Extensive remodeling of the presynaptic cytomatrix upon homeostatic adaptation to network activity silencing. J. Neurosci. 31: 10189– 10200 10.1523/JNEUROSCI.2088-11.2011 21752995 PMC6623065 · DOI
  47. Lee K.J. Park I.S. Kim H. Greenough W.T. Pak D.T. Rhyu I.J. 2013a Motor skill training induces coordinated strengthening and weakening between neighboring synapses. J. Neurosci. 33: 9794– 9799 10.1523/JNEUROSCI.0848-12.2013 23739975 PMC3865495 · DOI
  48. Lee K.J. Queenan B.N. Rozeboom A.M. Bellmore R. Lim S.T. Vicini S. Pak D.T. 2013b Mossy fiber-CA3 synapses mediate homeostatic plasticity in mature hippocampal neurons. Neuron. 77: 99– 114 10.1016/j.neuron.2012.10.033 23312519 PMC3545206 · DOI
  49. Lee S.J. Escobedo-Lozoya Y. Szatmari E.M. Yasuda R. 2009 Activation of CaMKII in single dendritic spines during long-term potentiation. Nature. 458: 299– 304 10.1038/nature07842 19295602 PMC2719773 · DOI · Paper page
  50. Lindskog M. Li L. Groth R.D. Poburko D. Thiagarajan T.C. Han X. Tsien R.W. 2010 Postsynaptic GluA1 enables acute retrograde enhancement of presynaptic function to coordinate adaptation to synaptic inactivity. Proc. Natl. Acad. Sci. USA. 107: 21806– 21811 10.1073/pnas.1016399107 21098665 PMC3003060 · DOI
  51. Lisman J.E. Raghavachari S. Tsien R.W. 2007 The sequence of events that underlie quantal transmission at central glutamatergic synapses. Nat. Rev. Neurosci. 8: 597– 609 10.1038/nrn2191 17637801 · DOI
  52. Lledo P.M. Zhang X. Südhof T.C. Malenka R.C. Nicoll R.A. 1998 Postsynaptic membrane fusion and long-term potentiation. Science. 279: 399– 403 10.1126/science.279.5349.399 9430593 · DOI · Paper page
  53. Loebel A. Le Bé J.V. Richardson M.J. Markram H. Herz A.V. 2013 Matched pre- and post-synaptic changes underlie synaptic plasticity over long time scales. J. Neurosci. 33: 6257– 6266 10.1523/JNEUROSCI.3740-12.2013 23575825 PMC6619066 · DOI
  54. Lu Y. Allen M. Halt A.R. Weisenhaus M. Dallapiazza R.F. Hall D.D. Usachev Y.M. McKnight G.S. Hell J.W. 2007 Age-dependent requirement of AKAP150-anchored PKA and GluR2-lacking AMPA receptors in LTP. EMBO J. 26: 4879– 4890 10.1038/sj.emboj.7601884 17972919 PMC2099463 · DOI
  55. Lynch G.S. Dunwiddie T. Gribkoff V. 1977 Heterosynaptic depression: a postsynaptic correlate of long-term potentiation. Nature. 266: 737– 739 10.1038/266737a0 195211 · DOI · Paper page
  56. MacGillavry H.D. Song Y. Raghavachari S. Blanpied T.A. 2013 Nanoscale scaffolding domains within the postsynaptic density concentrate synaptic AMPA receptors. Neuron. 78: 615– 622 10.1016/j.neuron.2013.03.009 23719161 PMC3668352 · DOI · Paper page
  57. Man H.Y. 2011 GluA2-lacking, calcium-permeable AMPA receptors—inducers of plasticity? Curr. Opin. Neurobiol. 21: 291– 298 10.1016/j.conb.2011.01.001 21295464 PMC3092818 · DOI · Paper page
  58. McGeachie A.B. Skrzypiec A.E. Cingolani L.A. Letellier M. Pawlak R. Goda Y. 2012 β3 integrin is dispensable for conditioned fear and hebbian forms of plasticity in the hippocampus. Eur. J. Neurosci. 36: 2461– 2469 10.1111/j.1460-9568.2012.08163.x 22748100 PMC5122446 · DOI
  59. Mitra A. Mitra S.S. Tsien R.W. 2012 Heterogeneous reallocation of presynaptic efficacy in recurrent excitatory circuits adapting to inactivity. Nat. Neurosci. 15: 250– 257 10.1038/nn.3004 22179109 PMC3558750 · DOI
  60. Müller M. Pym E.C. Tong A. Davis G.W. 2011 Rab3-GAP controls the progression of synaptic homeostasis at a late stage of vesicle release. Neuron. 69: 749– 762 10.1016/j.neuron.2011.01.025 21338884 PMC3059509 · DOI
  61. Müller M. Liu K.S. Sigrist S.J. Davis G.W. 2012 RIM controls homeostatic plasticity through modulation of the readily-releasable vesicle pool. J. Neurosci. 32: 16574– 16585 10.1523/JNEUROSCI.0981-12.2012 23175813 PMC3523185 · DOI
  62. Murthy V.N. Schikorski T. Stevens C.F. Zhu Y. 2001 Inactivity produces increases in neurotransmitter release and synapse size. Neuron. 32: 673– 682 10.1016/S0896-6273(01)00500-1 11719207 · DOI · Paper page
  63. Ohno-Shosaku T. Tanimura A. Hashimotodani Y. Kano M. 2012 Endocannabinoids and retrograde modulation of synaptic transmission. Neuroscientist. 18: 119– 132 10.1177/1073858410397377 21531987 · DOI
  64. Okuda T. Yu L.M. Cingolani L.A. Kemler R. Goda Y. 2007 beta-Catenin regulates excitatory postsynaptic strength at hippocampal synapses. Proc. Natl. Acad. Sci. USA. 104: 13479– 13484 10.1073/pnas.0702334104 17679699 PMC1948936 · DOI
  65. Opazo P. Labrecque S. Tigaret C.M. Frouin A. Wiseman P.W. De Koninck P. Choquet D. 2010 CaMKII triggers the diffusional trapping of surface AMPARs through phosphorylation of stargazin. Neuron. 67: 239– 252 10.1016/j.neuron.2010.06.007 20670832 · DOI
  66. Park M. Salgado J.M. Ostroff L. Helton T.D. Robinson C.G. Harris K.M. Ehlers M.D. 2006 Plasticity-induced growth of dendritic spines by exocytic trafficking from recycling endosomes. Neuron. 52: 817– 830 10.1016/j.neuron.2006.09.040 17145503 PMC1899130 · DOI · Paper page
  67. Peixoto R.T. Kunz P.A. Kwon H. Mabb A.M. Sabatini B.L. Philpot B.D. Ehlers M.D. 2012 Transsynaptic signaling by activity-dependent cleavage of neuroligin-1. Neuron. 76: 396– 409 10.1016/j.neuron.2012.07.006 23083741 PMC3783515 · DOI
  68. Powell C.M. Schoch S. Monteggia L. Barrot M. Matos M.F. Feldmann N. Südhof T.C. Nestler E.J. 2004 The presynaptic active zone protein RIM1alpha is critical for normal learning and memory. Neuron. 42: 143– 153 10.1016/S0896-6273(04)00146-1 15066271 PMC3910111 · DOI · Paper page
  69. Pozo K. Goda Y. 2010 Unraveling mechanisms of homeostatic synaptic plasticity. Neuron. 66: 337– 351 10.1016/j.neuron.2010.04.028 20471348 PMC3021747 · DOI · Paper page
  70. Rabinowitch I. Segev I. 2008 Two opposing plasticity mechanisms pulling a single synapse. Trends Neurosci. 31: 377– 383 10.1016/j.tins.2008.05.005 18602704 · DOI
  71. Sáez I. Friedlander M.J. 2009 Plasticity between neuronal pairs in layer 4 of visual cortex varies with synapse state. J. Neurosci. 29: 15286– 15298 10.1523/JNEUROSCI.2980-09.2009 19955381 PMC2824571 · DOI
  72. Saglietti L. Dequidt C. Kamieniarz K. Rousset M.C. Valnegri P. Thoumine O. Beretta F. Fagni L. Choquet D. Sala C. 2007 Extracellular interactions between GluR2 and N-cadherin in spine regulation. Neuron. 54: 461– 477 10.1016/j.neuron.2007.04.012 17481398 · DOI · Paper page
  73. Scanziani M. Malenka R.C. Nicoll R.A. 1996 Role of intercellular interactions in heterosynaptic long-term depression. Nature. 380: 446– 450 10.1038/380446a0 8602244 · DOI · Paper page
  74. Schikorski T. Stevens C.F. 1997 Quantitative ultrastructural analysis of hippocampal excitatory synapses. J. Neurosci. 17: 5858– 5867 9221783 PMC6573206
  75. Schnell E. Sizemore M. Karimzadegan S. Chen L. Bredt D.S. Nicoll R.A. 2002 Direct interactions between PSD-95 and stargazin control synaptic AMPA receptor number. Proc. Natl. Acad. Sci. USA. 99: 13902– 13907 10.1073/pnas.172511199 12359873 PMC129795 · DOI · Paper page
  76. Schoch S. Castillo P.E. Jo T. Mukherjee K. Geppert M. Wang Y. Schmitz F. Malenka R.C. Südhof T.C. 2002 RIM1alpha forms a protein scaffold for regulating neurotransmitter release at the active zone. Nature. 415: 321– 326 10.1038/415321a 11797009 · DOI · Paper page
  77. Schuman E.M. Madison D.V. 1994 Locally distributed synaptic potentiation in the hippocampus. Science. 263: 532– 536 10.1126/science.8290963 8290963 · DOI
  78. Sheng M. Kim E. 2011 The postsynaptic organization of synapses. Cold Spring Harb. Perspect. Biol. 3 10.1101/cshperspect.a005678 PMC3225953 22046028 · DOI · Paper page
  79. Shi S. Hayashi Y. Esteban J.A. Malinow R. 2001 Subunit-specific rules governing AMPA receptor trafficking to synapses in hippocampal pyramidal neurons. Cell. 105: 331– 343 10.1016/S0092-8674(01)00321-X 11348590 · DOI · Paper page
  80. Shipman S.L. Nicoll R.A. 2012 A subtype-specific function for the extracellular domain of neuroligin 1 in hippocampal LTP. Neuron. 76: 309– 316 10.1016/j.neuron.2012.07.024 23083734 PMC3998838 · DOI
  81. Siegel G. Saba R. Schratt G. 2011 microRNAs in neurons: manifold regulatory roles at the synapse. Curr. Opin. Genet. Dev. 21: 491– 497 10.1016/j.gde.2011.04.008 21561760 · DOI
  82. Sjöström P.J. Rancz E.A. Roth A. Häusser M. 2008 Dendritic excitability and synaptic plasticity. Physiol. Rev. 88: 769– 840 10.1152/physrev.00016.2007 18391179 · DOI
  83. Stan A. Pielarski K.N. Brigadski T. Wittenmayer N. Fedorchenko O. Gohla A. Lessmann V. Dresbach T. Gottmann K. 2010 Essential cooperation of N-cadherin and neuroligin-1 in the transsynaptic control of vesicle accumulation. Proc. Natl. Acad. Sci. USA. 107: 11116– 11121 10.1073/pnas.0914233107 20534458 PMC2890764 · DOI
  84. Stellwagen D. Malenka R.C. 2006 Synaptic scaling mediated by glial TNF-alpha. Nature. 440: 1054– 1059 10.1038/nature04671 16547515 · DOI · Paper page
  85. Südhof T.C. Rizo J. 2011 Synaptic vesicle exocytosis. Cold Spring Harb. Perspect. Biol. 3: a005637 10.1101/cshperspect.a005637 22026965 PMC3225952 · DOI
  86. Suh Y.H. Terashima A. Petralia R.S. Wenthold R.J. Isaac J.T. Roche K.W. Roche P.A. 2010 A neuronal role for SNAP-23 in postsynaptic glutamate receptor trafficking. Nat. Neurosci. 13: 338– 343 10.1038/nn.2488 20118925 PMC2861127 · DOI
  87. Sun Q. Turrigiano G.G. 2011 PSD-95 and PSD-93 play critical but distinct roles in synaptic scaling up and down. J. Neurosci. 31: 6800– 6808 10.1523/JNEUROSCI.5616-10.2011 21543610 PMC3113607 · DOI · Paper page
  88. Suzuki K. Hayashi Y. Nakahara S. Kumazaki H. Prox J. Horiuchi K. Zeng M. Tanimura S. Nishiyama Y. Osawa S. 2012 Activity-dependent proteolytic cleavage of neuroligin-1. Neuron. 76: 410– 422 10.1016/j.neuron.2012.10.003 23083742 · DOI
  89. Tardin C. Cognet L. Bats C. Lounis B. Choquet D. 2003 Direct imaging of lateral movements of AMPA receptors inside synapses. EMBO J. 22: 4656– 4665 10.1093/emboj/cdg463 12970178 PMC212729 · DOI · Paper page
  90. Tavalin S.J. 2008 AKAP79 selectively enhances protein kinase C regulation of GluR1 at a Ca2+-calmodulin-dependent protein kinase II/protein kinase C site. J. Biol. Chem. 283: 11445– 11452 10.1074/jbc.M709253200 18305116 PMC2431053 · DOI
  91. Tavalin S.J. Colledge M. Hell J.W. Langeberg L.K. Huganir R.L. Scott J.D. 2002 Regulation of GluR1 by the A-kinase anchoring protein 79 (AKAP79) signaling complex shares properties with long-term depression. J. Neurosci. 22: 3044– 3051 11943807 PMC6757527
  92. Thiagarajan T.C. Lindskog M. Tsien R.W. 2005 Adaptation to synaptic inactivity in hippocampal neurons. Neuron. 47: 725– 737 10.1016/j.neuron.2005.06.037 16129401 · DOI
  93. Tokuoka H. Goda Y. 2008 Activity-dependent coordination of presynaptic release probability and postsynaptic GluR2 abundance at single synapses. Proc. Natl. Acad. Sci. USA. 105: 14656– 14661 10.1073/pnas.0805705105 18794522 PMC2567165 · DOI
  94. Tomita S. Stein V. Stocker T.J. Nicoll R.A. Bredt D.S. 2005 Bidirectional synaptic plasticity regulated by phosphorylation of stargazin-like TARPs. Neuron. 45: 269– 277 10.1016/j.neuron.2005.01.009 15664178 · DOI · Paper page
  95. Turrigiano G.G. 2008 The self-tuning neuron: synaptic scaling of excitatory synapses. Cell. 135: 422– 435 10.1016/j.cell.2008.10.008 18984155 PMC2834419 · DOI · Paper page
  96. Turrigiano G.G. Nelson S.B. 2000 Hebb and homeostasis in neuronal plasticity. Curr. Opin. Neurobiol. 10: 358– 364 10.1016/S0959-4388(00)00091-X 10851171 · DOI
  97. Tyler W.J. Perrett S.P. Pozzo-Miller L.D. 2002 The role of neurotrophins in neurotransmitter release. Neuroscientist. 8: 524– 531 10.1177/1073858402238511 12467374 PMC2810653 · DOI
  98. Urban N.T. Willig K.I. Hell S.W. Nägerl U.V. 2011 STED nanoscopy of actin dynamics in synapses deep inside living brain slices. Biophys. J. 101: 1277– 1284 10.1016/j.bpj.2011.07.027 21889466 PMC3164186 · DOI
  99. Vitureira N. Letellier M. White I.J. Goda Y. 2012 Differential control of presynaptic efficacy by postsynaptic N-cadherin and β-catenin. Nat. Neurosci. 15: 81– 89 10.1038/nn.2995 22138644 PMC3245860 · DOI
  100. Xu W. Tse Y.C. Dobie F.A. Baudry M. Craig A.M. Wong T.P. Wang Y.T. 2013 Simultaneous monitoring of presynaptic transmitter release and postsynaptic receptor trafficking reveals an enhancement of presynaptic activity in metabotropic glutamate receptor-mediated long-term depression. J. Neurosci. 33: 5867– 5877 10.1523/JNEUROSCI.1508-12.2013 23536098 PMC4138313 · DOI
  101. Yang Y. Wang X.B. Frerking M. Zhou Q. 2008 Delivery of AMPA receptors to perisynaptic sites precedes the full expression of long-term potentiation. Proc. Natl. Acad. Sci. USA. 105: 11388– 11393 10.1073/pnas.0802978105 18682558 PMC2496888 · DOI
  102. Yuste R. Bonhoeffer T. 2001 Morphological changes in dendritic spines associated with long-term synaptic plasticity. Annu. Rev. Neurosci. 24: 1071– 1089 10.1146/annurev.neuro.24.1.1071 11520928 · DOI · Paper page
  103. Zhao C. Dreosti E. Lagnado L. 2011 Homeostatic synaptic plasticity through changes in presynaptic calcium influx. J. Neurosci. 31: 7492– 7496 10.1523/JNEUROSCI.6636-10.2011 21593333 PMC3124754 · DOI

Cited by

Sorted by citations

Authors
Vitureira, N., & Goda, Y.
Affiliations
  • Universidad de la República de Uruguay (UY)
  • RIKEN Center for Brain Science (JP)
Corresponding author
  • Vitureira, Nathalia
  • Goda, Yukiko
Venue
Journal of Cell Biology
Published
2013-10-28
Volume
203
Issue
2
Pages
175-186
ISSN
  • 0021-9525 (ISSN-L)
  • 1540-8140
OpenAlex
W2203294387
Cited by
152
References
27
Citations by year
2026: 1 · 2025: 14 · 2024: 6 · 2023: 13 · 2022: 10 · 2021: 10 · 2020: 12 · 2019: 12 · 2018: 16 · 2017: 12 · 2016: 18 · 2015: 15 · 2014: 13
FWCI
1.58
Type
journal article
Language
en
Open access
Licence
cc-by-nc-sa
Locations
  • The Journal of Cell Biology (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-sa)
  • PubMed Central (publishedVersion, cc-by-nc-sa)
  • PubMed (publishedVersion)
Funders
  • European Commission
  • Comisión Sectorial de Investigación Científica
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Keywords
Hebbian plasticity, homeostatic plasticity, long-term potentiation, long-term depression, synaptic plasticity, memory, synaptic efficacy
MeSH terms
Animals, Cell Communication, Homeostasis, Humans, Nerve Net, Nerve Tissue Proteins, Synaptic Transmission, Neuronal Plasticity, Neurons, Synapses, Long-Term Potentiation, Long-Term Synaptic Depression

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