Dynamics of dendritic calcium transients evoked by quantal release at excitatory hippocampal synapses
Open accessAbstract
Synaptic N -methyl- d -aspartate (NMDA) receptors detect coincident pre- and postsynaptic activity and play a critical role in triggering changes in synaptic strength at central synapses. Despite intensive study of synaptic plasticity, relatively little is known about the magnitude and duration of calcium accumulation caused by unitary events at individual synapses. We used fluorescence imaging to detect NMDA receptor-mediated miniature synaptic calcium transients (MSCTs) caused by spontaneous release of synaptic vesicles in dendrites of cultured hippocampal neurons. MSCTs originated focally in dendritic regions <1 μm in length and decayed with a time constant of 0.35 ± 0.03 s. Multiple occurrences of MSCTs recorded at single sites had fluctuating amplitudes, with a coefficient of variation of 0.34. From the reduction in the spatial spread of MSCTs with decreasing concentration of indicator dye, we estimated that the dominant endogenous calcium buffer in dendrites is relatively immobile (diffusion coefficient between 10 and 50 μm 2 /s). We conclude that calcium rise caused by spontaneous quantal synaptic NMDA receptor activation ( i ) is variable, ( ii ) lasts for a time period briefer than previous measurements indicate, and ( iii ) is confined by endogenous calcium buffers to local dendritic regions even when synapses are not on spines.
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GCaMP6f was used to detect postsynaptic miniature spontaneous Ca2+ transients (mSCaTs) that arose in dendritic spines following NMDA receptor activation by spontaneous release.
“GCaMP6f was used to detect postsynaptic miniature spontaneous Ca2+ transients (mSCaTs) that arose in dendritic spines following NMDA receptor activation by spontaneous release46.”
From A trans-synaptic nanocolumn aligns neurotransmitter release to receptors (2016) · cites this paper as [46]
The Abstract reports fluorescence detection of NMDA receptor-mediated miniature calcium transients caused by spontaneous vesicle release in dendrites. But Methods > Calcium Imaging specifies fluo-3, not GCaMP6f, and the Discussion says the authors generally could not resolve spines; it does not establish that the observed transients arose in spines. (LLM, conf=0.91)
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Cites
A synaptic model of memory: long-term potentiation in the hippocampus
Bliss, T. V. P., & Collingridge, G. L. (1993) · Nature · doi:10.1038/361031a0 · Cited by 11,566 · see citing works
Bi, G.-Q., & Poo, M.-M. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-24-10464.1998 · Cited by 4,744 · see citing works
Magnesium gates glutamate-activated channels in mouse central neurones
Nowak, L. M., Bregestovski, P. D., Ascher, P., Herbet, A., & Prochiantz, A. (1984) · Nature · doi:10.1038/307462a0 · Cited by 4,033 · see citing works
Regulation of Synaptic Efficacy by Coincidence of Postsynaptic APs and EPSPs
Markram, H., Lübke, J., Frotscher, M., & Sakmann, B. (1997) · Science · doi:10.1126/science.275.5297.213 · Cited by 3,832 · see citing works
Voltage-dependent block by Mg2+ of NMDA responses in spinal cord neurones
Mayer, M. L., Westbrook, G. L., & Guthrie, P. B. (1984) · Nature · doi:10.1038/309261a0 · Cited by 2,906 · see citing works
Synaptotagmin I: A major Ca2+ sensor for transmitter release at a central synapse
Geppert, M., Goda, Y., Hammer, R. E., Li, C., Rosahl, T. W., Stevens, C. F., & Südhof, T. C. (1994) · Cell · doi:10.1016/0092-8674(94)90556-8 · Cited by 1,483 · see citing works
Self-citationRange of Messenger Action of Calcium Ion and Inositol 1,4,5-Trisphosphate
Allbritton, N. L., Meyer, T., & Stryer, L. (1992) · Science · doi:10.1126/science.1465619 · Cited by 1,156 · see citing works
Harris, K., & Stevens, J. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-08-02982.1989 · Cited by 1,073 · see citing works
Dendritic spines as basic functional units of neuronal integration
Yuste, R., & Denk, W. (1995) · Nature · doi:10.1038/375682a0 · Cited by 950 · see citing works
Optical Analysis of Synaptic Vesicle Recycling at the Frog Neuromuscular Junction
Betz, W. J., & Bewick, G. S. (1992) · Science · doi:10.1126/science.1553547 · Cited by 763 · see citing works
Bekkers, J. M., & Stevens, C. F. (1989) · Nature · doi:10.1038/341230a0 · Cited by 660 · see citing works
Self-citationHeterogeneous Release Properties of Visualized Individual Hippocampal Synapses
Murthy, V. N., B, T. J. S. A., & Stevens, C. F. (1997) · Neuron · doi:10.1016/s0896-6273(00)80301-3 · Cited by 596 · see citing works
Self-citationVoltage dependence of NMDA-activated macroscopic conductances predicted by single-channel kinetics
Jahr, C., & Stevens, C. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-09-03178.1990 · Cited by 569 · see citing works
Self-citationCa2+ buffering and action potential-evoked Ca2+ signaling in dendrites of pyramidal neurons
Helmchen, F., Imoto, K., & Sakmann, B. (1996) · Biophysical Journal · doi:10.1016/s0006-3495(96)79653-4 · Cited by 559 · see citing works
The kinetics of synaptic vesicle recycling measured at single presynaptic boutons
Ryan, T. A., REUTER, H., Wendland, B., Schweizer, F. E., Tsien, R. W., & Smith, S. J. (1993) · Neuron · doi:10.1016/0896-6273(93)90081-2 · Cited by 517 · see citing works
Facilitation and depression at single central synapses
Stevens, C. F., & Wang, Y. (1995) · Neuron · doi:10.1016/0896-6273(95)90223-6 · Cited by 502 · see citing works
Self-citationDendritic spines as individual neuronal compartments for synaptic Ca2+ responses
Müller, W. S., & Connor, J. A. (1991) · Nature · doi:10.1038/354073a0 · Cited by 479 · see citing works
Effects of rapid buffers on Ca2+ diffusion and Ca2+ oscillations
Wagner, J., & Keizer, J. (1994) · Biophysical Journal · doi:10.1016/s0006-3495(94)80500-4 · Cited by 479 · see citing works
Origin of variability in quantal size in cultured hippocampal neurons and hippocampal slices.
Bekkers, J. M., Richerson, G. B., & Stevens, C. F. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.14.5359 · Cited by 455 · see citing works
Self-citationMobile and immobile calcium buffers in bovine adrenal chromaffin cells.
Zhou, Z., & Neher, E. (1993) · The Journal of Physiology · doi:10.1113/jphysiol.1993.sp019813 · Cited by 426 · see citing works
Markram, H., Helm, P. J., & Sakmann, B. J. (1995) · The Journal of Physiology · doi:10.1113/jphysiol.1995.sp020708 · Cited by 387 · see citing works
Scanziani, M., Capogna, M., Gähwiler, B., & Thompson, S. (1992) · Neuron · doi:10.1016/0896-6273(92)90244-8 · Cited by 386 · see citing works
Regulation of hippocampal transmitter release during development and long-term potentiation.
Bolshakov, V. Y., & Siegelbaum, S. (1995) · Science · doi:10.1126/science.7569903 · Cited by 385 · see citing works
Koester, H. J., & Sakmann, B. J. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.16.9596 · Cited by 338 · see citing works
Subthreshold synaptic Ca2+ signalling in fine dendrites and spines of cerebellar Purkinje neurons
Eilers, J., Augustine, G. J., & Konnerth, A. (1995) · Nature · doi:10.1038/373155a0 · Cited by 321 · see citing works
Synaptic calcium transients in single spines indicate that NMDA receptors are not saturated
Mainen, Z. F., Malinow, R., & Svoboda, K. (1999) · Nature · doi:10.1038/20187 · Cited by 314 · see citing works
Properties of synaptic transmission at single hippocampal synaptic boutons
Liu, G., & Tsien, R. W. (1995) · Nature · doi:10.1038/375404a0 · Cited by 302 · see citing works
Two types of calcium response limited to single spines in cerebellar Purkinje cells.
Denk, W. T., Sugimori, M., & Llinas, R. H. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.18.8279 · Cited by 284 · see citing works
Vesicle pool mobilization during action potential firing at hippocampal synapses
Ryan, T. A., & Smith, S. J. (1995) · Neuron · doi:10.1016/0896-6273(95)90336-4 · Cited by 282 · see citing works
Synaptic vesicles retain their identity through the endocytic cycle
Murthy, V. N., & Stevens, C. F. (1998) · Nature · doi:10.1038/33152 · Cited by 268 · see citing works
Self-citationIndependent regulation of calcium revealed by imaging dendritic spines
Guthrie, P. B., Segal, M., & Kater, S. B. (1991) · Nature · doi:10.1038/354076a0 · Cited by 262 · see citing works
Reversal of synaptic vesicle docking at central synapses
Murthy, V. N., & Stevens, C. F. (1999) · Nature Neuroscience · doi:10.1038/9149 · Cited by 254 · see citing works
Self-citationRaastad, M., Storm, J. F., & Andersen, P. N. (1992) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1992.tb00114.x · Cited by 250 · see citing works
Malenka, R. C., Lancaster, B., & Zucker, R. S. (1992) · Neuron · doi:10.1016/0896-6273(92)90227-5 · Cited by 250 · see citing works
Quantal release of neurotransmitter and long-term potentiation.
Stevens, C. (1993) · Cell · doi:10.1016/s0092-8674(05)80028-5 · Cited by 222 · see citing works
Self-citationCalcium permeability of the N-methyl-D-aspartate receptor channel in hippocampal neurons in culture.
Jahr, C. E., & Stevens, C. F. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.24.11573 · Cited by 189 · see citing works
Self-citationLoose-patch recordings of single quanta at individual hippocampal synapses
Forti, L., Bossi, M., Bergamaschi, A., Villa, A., & Malgaroli, A. (1997) · Nature · doi:10.1038/42251 · Cited by 180 · see citing works
Comparison of Hippocampal Dendritic Spines in Culture and in Brain
Boyer, C., Schikorski, T., & Stevens, C. F. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-14-05294.1998 · Cited by 144 · see citing works
Self-citationLow Mobility of the Ca2+ Buffers in Axons of Cultured Aplysia Neurons
Gabso, M., Neher, E., & Spira, M. E. (1997) · Neuron · doi:10.1016/s0896-6273(00)81247-7 · Cited by 129 · see citing works
Imaging calcium dynamics in dendritic spines
Denk, W. T., Yuste, R., Svoboda, K., & Tank, D. W. (1996) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(96)80122-x · Cited by 129 · see citing works
Visualization of quantal synaptic transmission by dendritic calcium imaging.
Murphy, T. H., Baraban, J., Wier, W., & Blatter, L. (1994) · Science · doi:10.1126/science.7904774 · Cited by 76 · see citing works
Imaging of calcium variations in living dendritic spines of cultured rat hippocampal neurons.
Segal, M. (1995) · The Journal of Physiology · doi:10.1113/jphysiol.1995.sp020811 · Cited by 58 · see citing works
Murphy, T. H., Baraban, J., & Wier, W. (1995) · Neuron · doi:10.1016/0896-6273(95)90073-x · Cited by 42 · see citing works
Flagged first, then by citations
2 of the 45 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Origin of Slow Cortical Oscillations in Deafferented Cortical Slabs
Timofeev, I. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.12.1185 · Cited by 710 · see citing works
A trans-synaptic nanocolumn aligns neurotransmitter release to receptors
Tang, A.-H., Chen, H., Li, T. P., Metzbower, S. R., MacGillavry, H. D., & Blanpied, T. A. (2016) · Nature · doi:10.1038/nature19058 · Cited by 677 · see citing works
A Calcium-Dependent Feedback Mechanism Participates in Shaping Single NMDA Miniature EPSCs
Umemiya, M., Chen, N., Raymond, L. A., & Murphy, T. H. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-01-00001.2001 · Cited by 450 · see citing works
St-Pierre, F., Marshall, J. D., Yang, Y., Gong, Y., Schnitzer, M. J., & Lin, M. Z. (2014) · Nature Neuroscience · doi:10.1038/nn.3709 · Cited by 402 · see citing works
From form to function: calcium compartmentalization in dendritic spines
Yuste, R., Majewska, A. K., & Holthoff, K. (2000) · Nature Neuroscience · doi:10.1038/76609 · Cited by 370 · see citing works
Ca(2+) signaling in dendritic spines.
Sabatini, B., Maravall, M., & Svoboda, K. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00218-x · Cited by 340 · see citing works
Aberra, A. S., Wang, B., Grill, W. M., & Peterchev, A. V. (2019) · Brain stimulation · doi:10.1016/j.brs.2019.10.002 · Cited by 323 · see citing works
Calcium Signaling in Neuronal Motility
Zheng, J. Q., & Poo, M.-M. (2007) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.23.090506.123221 · Cited by 292 · see citing works
Regulation of Dendritic Protein Synthesis by Miniature Synaptic Events
Sutton, M. A., Wall, N. R., Aakalu, G., & Schuman, E. (2004) · Science · doi:10.1126/science.1096202 · Cited by 286 · see citing works
Activity-Dependent Clustering of Functional Synaptic Inputs on Developing Hippocampal Dendrites
Kleindienst, T., Winnubst, J., Roth-Alpermann, C., Bonhoeffer, T., & Löhmann, C. (2011) · Neuron · doi:10.1016/j.neuron.2011.10.015 · Cited by 247 · see citing works
Calcium Microdomains in Aspiny Dendrites
Goldberg, J. H., Tamas, G., Aronov, D., & Yuste, R. (2003) · Neuron · doi:10.1016/s0896-6273(03)00714-1 · Cited by 212 · see citing works
Atasoy, D., Ertunç, M., Moulder, K., Blackwell, J., Chung, C.-Y., Su, J.-Z., & Kavalali, E. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.2432-08.2008 · Cited by 201 · see citing works
Steigerwald, F., Schulz, T. W., Schenker, L. T., Kennedy, M., Seeburg, P., & Köhr, G. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-12-04573.2000 · Cited by 204 · see citing works
Calcium Time Course as a Signal for Spike-Timing–Dependent Plasticity
Rubin, J. E., Gerkin, R. C., Bi, G., & Chow, C. C. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00803.2004 · Cited by 187 · see citing works
Disentangling calcium-driven astrocyte physiology
Rusakov, D. A. (2015) · Nature reviews. Neuroscience · doi:10.1038/nrn3878 · Cited by 170 · see citing works
Gebara, E., Zanoletti, O., Ghosal, S., Grosse, J., Schneider, B. L., Knott, G. W., Astori, S., & Sandi, C. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.12.003 · Cited by 144 · see citing works
Mechanisms Underlying the Rules for Associative Plasticity at Adult Human Neocortical Synapses
Verhoog, M. B., Goriounova, N. A., Obermayer, J., Stroeder, J., Hjorth, J. J. J., Testa-Silva, G., Baayen, J. C., de Kock, C. P. J., Meredith, R. M., & Mansvelder, H. D. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.3158-13.2013 · Cited by 127 · see citing works
Inhibition of NMDARs in the nucleus reticularis of the thalamus produces delta frequency bursting
Zang, Y. (2009) · Frontiers in Neural Circuits · doi:10.3389/neuro.04.020.2009 · Cited by 127 · see citing works
Calcium dynamics of spines depend on their dendritic location
Holthoff, K., Tsay, D., & Yuste, R. (2002) · Neuron · doi:10.1016/s0896-6273(02)00576-7 · Cited by 117 · see citing works
Bellamy, T. C., & Garthwaite, J. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m006677200 · Cited by 111 · see citing works
Quantal variability at glutamatergic synapses in area CA1 of the rat neonatal hippocampus
Hanse, E., & Gustafsson, B. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.0467i.x · Cited by 109 · see citing works
Kapur, A., Yeckel, M. F., & Johnston, D. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00293-7 · Cited by 87 · see citing works
Burkhalter, A., Gonchar, Y., Mellor, R. L., & Nerbonne, J. M. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2599-06.2006 · Cited by 79 · see citing works
Modulation of spontaneous quantal release of neurotransmitters in the hippocampus.
Bouron, A. (2001) · Progress in neurobiology · doi:10.1016/s0301-0082(00)00053-8 · Cited by 83 · see citing works
Timing in synaptic plasticity: from detection to integration
Bi, G., & Rubin, J. E. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.02.002 · Cited by 74 · see citing works
The shaping of nitric oxide signals by a cellular sink
Griffiths, C., & Garthwaite, J. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.00855.x · Cited by 70 · see citing works
Towards neuro-memory-chip: Imprinting multiple memories in cultured neural networks
Baruchi, I., & Ben‐Jacob, E. (2007) · Physical Review E · doi:10.1103/physreve.75.050901 · Cited by 66 · see citing works
A role for ERKII in synaptic pattern selectivity on the time‐scale of minutes
Ajay, S. M., & Bhalla, U. S. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03725.x · Cited by 64 · see citing works
Input transformation by dendritic spines of pyramidal neurons
Araya, R. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00141 · Cited by 58 · see citing works
Sinnen, B. L., Bowen, A. B., Gibson, E. S., & Kennedy, M. J. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1603-16.2016 · Cited by 57 · see citing works
Nifedipine facilitates neurotransmitter release independently of calcium channels
Hirasawa, M., & Pittman, Q. J. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0936131100 · Cited by 52 · see citing works
Dendritic SNAREs add a new twist to the old neuron theory
Ovsepian, S. V., & Dolly, J. O. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1017235108 · Cited by 50 · see citing works
Layer‐specific alterations to CA1 dendritic spines in a mouse model of Alzheimer's disease
Merino‐Serrais, P., Knafo, S., Alonso‐Nanclares, L., Fernaud-Espinosa, I., & DeFelipe, J. (2010) · Hippocampus · doi:10.1002/hipo.20861 · Cited by 49 · see citing works
Kaiser, K. M. M., Lübke, J. H. R., Zilberter, Y., & Sakmann, B. J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2852-03.2004 · Cited by 49 · see citing works
A Single-Compartment Model of Calcium Dynamics in Nerve Terminals and DendritesPreprint
Helmchen, F., & Tank, D. W. (2015) · Cold Spring Harbor Protocols · doi:10.1101/pdb.top085910 · Cited by 47 · see citing works
Korkotian, E., & Segal, M. (2006) · Cell Calcium · doi:10.1016/j.ceca.2006.08.008 · Cited by 43 · see citing works
Aoki, C. J., Fujisawa, S., Mahadomrongkul, V., Shah, P. J., Nader, K., & Erişir, A. (2003) · Brain Research · doi:10.1016/s0006-8993(02)03962-8 · Cited by 43 · see citing works
Calcium dynamics at developing synapses: mechanisms and functions
Michaelsen, K., & Löhmann, C. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07341.x · Cited by 39 · see citing works
Functional NMDA Receptors at Axonal Growth Cones of Young Hippocampal Neurons
Wang, P. Y., Petralia, R. S., Wang, Y.-X., Wenthold, R. J., & Brenowitz, S. D. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5639-10.2011 · Cited by 38 · see citing works
Local signaling with molecular diffusion as a decoder of Ca2+ signals in synaptic plasticity
Naoki, H., Sakumura, Y., & Ishii, S. (2005) · Molecular Systems Biology · doi:10.1038/msb4100035 · Cited by 32 · see citing works
Kubota, Y., Putkey, J. A., Shouval, H. Z., & Waxham, M. N. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00876.2007 · Cited by 29 · see citing works
Distance-dependent gradient in NMDAR-driven spine calcium signals along tapering dendrites
Walker, A., Neves, G., Grillo, F. W., Jackson, R. E., Rigby, M., O’Donnell, C., Lowe, A., Vizcay‐Barrena, G., Fleck, R. A., & Burrone, J. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1607462114 · Cited by 25 · see citing works
The role of Plasma Membrane Calcium ATPases (PMCAs) in neurodegenerative disorders
Hajieva, P., Baeken, M. W., & Moosmann, B. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2017.09.033 · Cited by 27 · see citing works
Studying complex system: calcium oscillations as attractor of cell differentiation
Pinto, M. C. X., Tonelli, F. M. P., Vieira, A. L. G., Kihara, A. H., Ulrich, H., & Resende, R. R. (2015) · Integrative Biology · doi:10.1039/c5ib00285k · Cited by 25 · see citing works
Olfactory learning‐induced morphological modifications in single dendritic spines of young rats
Knafo, S., Libersat, F., & Barkai, E. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04041.x · Cited by 23 · see citing works
Na+-Ca2+Exchanger Controls the Gain of the Ca2+Amplifier in the Dendrites of Amacrine Cells
Hurtado, J., Borges, S., & Wilson, M. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00130.2002 · Cited by 23 · see citing works
Otsu, Y., & Murphy, T. H. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2060-04.2004 · Cited by 21 · see citing works
GHz Ultrasonic Chip-Scale Device Induces Ion Channel Stimulation in Human Neural Cells
Balasubramanian, P. S., Singh, A., Xu, C., & Lal, A. (2020) · Scientific Reports · doi:10.1038/s41598-020-58133-0 · Cited by 20 · see citing works
Separate Ca2+Sources Are Buffered by Distinct Ca2+Handling Systems inAplysiaNeuroendocrine Cells
Groten, C. J., Rebane, J. T., Blohm, G., & Magoski, N. S. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.6384-11.2013 · Cited by 16 · see citing works
Induction and Consolidation of Calcium-Based Homo- and Heterosynaptic Potentiation and Depression
Li, Y., Kulvičius, T., & Tetzlaff, C. (2016) · PLoS ONE · doi:10.1371/journal.pone.0161679 · Cited by 15 · see citing works
Yeung, L. C., Castellani, G., & Shouval, H. Z. (2004) · Physical Review E · doi:10.1103/physreve.69.011907 · Cited by 13 · see citing works
Chiou, L., & Chou, H. H. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00348-1 · Cited by 13 · see citing works
Mackenzie, P. J., Kenner, G. S., Prange, O., & Murphy, T. H. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00089-0 · Cited by 10 · see citing works
Rao, S. P., & Sikdar, S. K. (2004) · Brain Research · doi:10.1016/j.brainres.2004.06.068 · Cited by 10 · see citing works
Volman, V., Levine, H., Ben‐Jacob, E., & B, T. J. S. A. (2009) · Journal of Neurophysiology · doi:10.1152/jn.00260.2009 · Cited by 9 · see citing works
AMPA receptor-mediated miniature synaptic calcium transients in GluR2 null mice.
Wang, S., Jia, Z.-P., Roder, J., & Murphy, T. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.88.1.29 · Cited by 8 · see citing works
Barbee, K. A., Parikh, J., Liu, Y., Buerk, D. G., & Jaron, D. (2018) · Cellular and Molecular Bioengineering · doi:10.1007/s12195-018-0520-4 · Cited by 6 · see citing works
A Phenomenological Calcium-Based Model of STDP
Gerkin, R. C., Bi, G., & Rubin, J. E. (2010) · Springer eBooks · doi:10.1007/978-1-4419-0996-1_20 · Cited by 6 · see citing works
All-optical mapping of Ca2+ transport and homeostasis in dendrites
Hayward, R. F., & Cohen, A. E. (2024) · Cell Calcium · doi:10.1016/j.ceca.2024.102983 · Cited by 5 · see citing works
Padmashri, R., Ganguly, A., Mondal, P. P., Rajan, K., & Sikdar, S. K. (2005) · Cell Calcium · doi:10.1016/j.ceca.2005.11.003 · Cited by 5 · see citing works
Beaupré, F., Bilodeau, A., Wiesner, T., Leclerc, G., Lemieux, M., Nadeau, G., Castonguay, K., Fan, B., Labrecque, S., Hložek, R., et al. (2024) · Digital Discovery · doi:10.1039/d4dd00197d · Cited by 2 · see citing works
Murphy, J. G., Gutzmann, J. J., Lin, L., Hu, J., Petralia, R. S., Wang, Y., & Hoffman, D. A. (2022) · Cell Reports · doi:10.1016/j.celrep.2021.110264 · Cited by 1 · see citing works
N-Methyl-D-Aspartate Receptors
Iacobucci, G. J., & Popescu, G. (2019) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780190669164.013.16 · Cited by 1 · see citing works
Fan, B., Bilodeau, A., Beaupré, F., Wiesner, T., Gagné, C., Lavoie‐Cardinal, F., & Hložek, R. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.13.711411
Synaptic plasticity and Hebbian cell assemblies
Gerkin, R. C. (2008) · D-Scholarship@Pitt (University of Pittsburgh)
The fine scale structure of synaptic inputs in developing hippocampal neurons
Kleindienst, T. (2010) · Electronic Theses of LMU Munich (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.12662
Jafri, H., Thomas, S. J., Yang, S. H., Cain, R. E., & Dalva, M. B. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.13.637710 · Cited by 1 · see citing works
Optical Single-Channel Recording via Diffusional Confinement in Membrane Tethers
Howell, M. R., & Cohen, A. E. (2025) · ACS Nano · doi:10.1021/acsnano.5c07589
- Authors
- Murthy, V. N., Sejnowski, T. J., & Stevens, C. F.
- Affiliations
- Howard Hughes Medical Institute (US)
- Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138; Howard Hughes Medical Institute, Molecular Neurobiology Lab, Salk Institute, La Jolla, CA 92037; and Howard Hughes Medical Institute, Computational Neurobiology Lab, Salk Institute, La Jolla, CA 92037, and Department of Biology, University of California at San Diego, La Jolla, CA 92093
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2000-01-18
- Volume
- 97
- Issue
- 2
- Pages
- 901-906
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC15428
- OpenAlex
- W1968581566
- Cited by
- 70
- References
- 45
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 3 · 2022: 2 · 2020: 2 · 2019: 2 · 2018: 2 · 2017: 1 · 2016: 3 · 2015: 3 · 2014: 2 · 2013: 2
- FWCI
- 2.33
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institutes of Health (5r01mh046482-03, 5r01ns012961-22)
- National Institute of Mental Health (MH-46482)
- National Institute of Neurological Disorders and Stroke (NS-12961)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- dendritic calcium transients, NMDA receptor, hippocampal neurons, synaptic plasticity, dendritic calcium signaling
- MeSH terms
- Quaternary Ammonium Compounds, Aniline Compounds, Animals, Calcium, Cells, Cultured, Dendrites, Fluorescent Dyes, Hippocampus, Magnesium, Models, Biological, Pyridinium Compounds, Synapses, Synaptic Vesicles, Time Factors, Xanthenes, Receptors, N-Methyl-D-Aspartate, Cadmium Chloride, Excitatory Postsynaptic Potentials
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