Selective Induction of LTP and LTD by Postsynaptic [Ca2+]i Elevation
Open accessAbstract
Selective Induction of LTP and LTD by Postsynaptic [Ca 2+]i Elevation. Long-term potentiation (LTP) and long-term depression (LTD), two prominent forms of synaptic plasticity at glutamatergic afferents to CA1 hippocampal pyramidal cells, are both triggered by the elevation of postsynaptic intracellular calcium concentration ([Ca 2+]i). To understand how one signaling molecule can be responsible for triggering two opposing forms of synaptic modulation, different postsynaptic [Ca 2+]i elevation patterns were generated by a new caged calcium compound nitrophenyl-ethylene glycol-bis(β-aminoethyl ether)- N, N, N′, N′-tetraacetic acid in CA1 pyramidal cells. We found that specific patterns of [Ca 2+]i elevation selectively activate LTP or LTD. In particular, only LTP was triggered by a brief increase of [Ca 2+]i with relatively high magnitude, which mimics the [Ca 2+]i rise during electrical stimulation typically used to induce LTP. In contrast, a prolonged modest rise of [Ca 2+]i reliably induced LTD. An important implication of the results is that both the amplitude and the duration of an intracellular chemical signal can carry significant biological information.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Nitr-5 can evoke either an enhancement or a depression, depending on the amplitude and the duration of the Ca2+ signal.
“Further studies showed that nitr-5 can evoke either an enhancement or a depression, depending on the amplitude and the duration of the Ca2+ signal (181).”
From Synaptic memory and CaMKII (2023) · cites this paper as [181]
The Results section says earlier nitr-5 experiments produced either LTP (enhancement) or LTD (depression) after brief calcium elevations. But the paper attributes selective effects of calcium-signal amplitude and duration to its experiments with nitrophenyl-EGTA; it says nitr-5 could not produce a very high or prolonged calcium rise. Individual passage page numbers are unavailable in our copy. (LLM, conf=0.88)
Experimental — accuracy not yet measuredBrief large-amplitude signals favor potentiation, whereas more modest long-duration signals favor depression.
“Brief large-amplitude signals favor potentiation, whereas more modest long-duration signals favor depression (181).”
From Synaptic memory and CaMKII (2023) · cites this paper as [181]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Ca2+ 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
Flagged first, then by citations
Research works printed but not linked: 3
- BISHOP, C. M. Neural Networks for Pattern Recognition. Oxford: Clarendon Press, 1995.
- ELLIS-DAVIES, G.C.R. AND KAPLAN, J. H. Nitrophenyl-EGTA, a photolabile chelator that selectively binds Ca 2ϩ with high affinity and releases it rapidly upon photolysis. Proc. Natl. Acad. Sci. USA 91: 187-191, 1994.
- LISMAN, J. A mechanism for the Hebb and the anti-Hebb processes under- lying learning and memory. Proc. Natl. Acad. Sci. USA 86: 9574 -9578, 1989.
Cited by
Sorted by citations
Long-Term Potentiation--A Decade of Progress?
Malenka, R. C., & Nicoll, A. R. A. (1999) · Science · doi:10.1126/science.285.5435.1870 · Cited by 2,729 · see citing works
Spike Timing–Dependent Plasticity: A Hebbian Learning Rule
Caporale, N., & Dan, Y. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.060407.125639 · Cited by 1,997 · see citing works
Shankar, G. M., Bloodgood, B. L., Townsend, M., Walsh, D. M., Selkoe, D. J., & Sabatini, B. L. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.4970-06.2007 · Cited by 1,592 · see citing works
Regulation of NMDA receptor subunit expression and its implications for LTD, LTP, and metaplasticity
Yashiro, K., & Philpot, B. D. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.07.046 · Cited by 649 · see citing works
Kim, S., Du, C., Sheridan, P., Ma, W., Choi, S., & Lu, W. D. (2015) · Nano Letters · doi:10.1021/acs.nanolett.5b00697 · Cited by 603 · see citing works
Regulation of AMPA receptor lateral movements
Borgdorff, A. J., & Choquet, D. (2002) · Nature · doi:10.1038/nature00780 · Cited by 542 · see citing works
Neuronal calcium sensor proteins: generating diversity in neuronal Ca2+ signalling
Burgoyne, R. D. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2093 · Cited by 527 · see citing works
Plasticity of Cortical Excitatory-Inhibitory Balance
Froemke, R. C. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071714-034002 · Cited by 458 · see citing works
Ageing and diabetes: implications for brain function
Biessels, G. J., van der Heide, L. P., Kamal, A., Bleys, R. L. A. W., & Gispen, W. H. (2002) · European Journal of Pharmacology · doi:10.1016/s0014-2999(02)01486-3 · Cited by 458 · see citing works
Du, C., Ma, W., Chang, T., Sheridan, P., & Lu, W. D. (2015) · Advanced Functional Materials · doi:10.1002/adfm.201501427 · Cited by 444 · see citing works
The BCM theory of synapse modification at 30: interaction of theory with experiment
Cooper, L. N., & Bear, M. F. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3353 · Cited by 395 · see citing works
GABA promotes the competitive selection of dendritic spines by controlling local Ca2+ signaling
Hayama, T., Noguchi, J., Watanabe, S., Takahashi, N., Hayashi-Takagi, A., Ellis-Davies, G. C. R., Matsuzaki, M., & Kasai, H. (2013) · Nature Neuroscience · doi:10.1038/nn.3496 · Cited by 193 · see citing works
Insufficient Sleep Reversibly Alters Bidirectional Synaptic Plasticity and NMDA Receptor Function
Kopp, C., Longordo, F., Nicholson, J. R., & Lüthi, A. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.2702-06.2006 · Cited by 192 · see citing works
Akashi, K., Kakizaki, T., Kamiya, H., Fukaya, M., Yamasaki, M., Abe, M., Natsume, R., Watanabe, M., & Sakimura, K. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5531-08.2009 · Cited by 163 · see citing works
Shifman, J. M., Choi, M. H., Mihalas, S., Mayo, S. L., & Kennedy, M. B. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0606433103 · Cited by 143 · 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
Nicoll, R. A., & Schulman, H. (2023) · Physiological Reviews · doi:10.1152/physrev.00034.2022 · Cited by 126 · see citing works
“First, a photosensitive caged Ca 2 1 was employed (177, 181 – 183).”
BackgroundMethodIs Persistent Activity of Calcium/Calmodulin-Dependent Kinase Required for the Maintenance of LTP?
Chen, H.-X., Otmakhov, N., Strack, S., Colbran, R. J., & Lisman, J. E. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.4.1368 · Cited by 126 · 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
Hojo, Y., Higo, S., Kawato, S., Hatanaka, Y., Ooishi, Y., Murakami, G., Ishii, H., Komatsuzaki, Y., Ogiue-Ikeda, M., Mukai, H., et al. (2011) · Frontiers in Endocrinology · doi:10.3389/fendo.2011.00043 · Cited by 86 · see citing works
Yuan, Q., Harley, C. W., Bruce, J. C., Darby-King, A., & McLean, J. H. (2000) · Learning & Memory · doi:10.1101/lm.35900 · Cited by 73 · see citing works
Ghasemian-Shirvan, E., Mosayebi-Samani, M., Farnad, L., Kuo, M.-F., Meesen, R. L. J., & Nitsche, M. A. (2022) · Brain Stimulation · doi:10.1016/j.brs.2022.01.011 · Cited by 34 · see citing works
- Authors
- Yang, S.-N., Tang, Y.-G., & Zucker, R. S.
- Affiliations
- University of California, Berkeley (US)
- Venue
- Journal of Neurophysiology
- Publisher
- American Physiological Society
- Published
- 1999-02-01
- Volume
- 81
- Issue
- 2
- Pages
- 781-787
- ISSN
- 0022-3077 (ISSN-L)
- 1522-1598
- OpenAlex
- W1957331510
- Cited by
- 534
- References
- 1
- Citations by year
- 2026: 7 · 2025: 19 · 2024: 13 · 2023: 20 · 2022: 12 · 2021: 12 · 2020: 14 · 2019: 22 · 2018: 16 · 2017: 15 · 2016: 19 · 2015: 21 · 2014: 15 · 2013: 24 · 2012: 16
- FWCI
- 7.83
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Neurophysiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Karolinska Institutet
- National Institute of Neurological Disorders and Stroke (NS-15114, R01NS015114)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- long-term potentiation, long-term depression, postsynaptic calcium, intracellular calcium elevation, synaptic plasticity, CA1 pyramidal neurons, hippocampus, caged calcium, glutamatergic synapses
- MeSH terms
- Animals, Calcium, Chelating Agents, Egtazic Acid, Hippocampus, Intracellular Fluid, Neuronal Plasticity, Photolysis, Synapses, Rats, Sprague-Dawley, Long-Term Potentiation, Patch-Clamp Techniques, Excitatory Postsynaptic Potentials, Rats, In Vitro Techniques
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review