Chapter 34 Synaptic modulation by neurotrophic factors
Open accessAbstract
This chapter focuses on the recent results on synaptic modulation by neurotrophic factors and discusses their physiological implications. Several recent studies have indeed shown rapid synaptic modulation by a number of neurotrophic factors, including neurotrophins—a family of factors related to nerve growth factors (NGF)—as well as ciliary neurotrophic factor (CNTF)—a factor in the cytokine family known to promote the survival of a variety of neuronal populations. The effects of neurotrophins on synaptic currents can be accounted for by presynaptic actions of the factors—namely, a potentiation of transmitter secretion, either in the availability of transmitter containing vesicles or in the probability of vesicular exocytosis. The potential role of neurotrophins in regulating the maturation of synaptic functions is also addressed in cell culture. An important issue that remains to be addressed is the biological relevance of the synaptic modulation by neurotrophic factors observed in various in vitro preparations.
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?
BDNF influences neuronal plasticity by facilitating neurotransmitter release, increasing vesicular docking, enhancing glutamate-evoked post-synaptic responses and facilitating hippocampal and cortical long-term potentiation.
“BDNF influences neuronal plasticity by facilitating neurotransmitter release29, increasing vesicular docking, enhancing glutamate-evoked post-synaptic responses30 and facilitating hippocampal and cortical long-term potentiation31.”
From Neuroprotective effects of brain-derived neurotrophic factor in rodent and primate models of Alzheimer's disease (2009) · cites this paper as [29]
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
Long-Lasting Neurotrophin-Induced Enhancement of Synaptic Transmission in the Adult Hippocampus
Kang, H., & Schuman, E. M. (1995) · Science · doi:10.1126/science.7886457 · Cited by 1,354 · see citing works
Neurotrophin-3: a Neurotrophic Factor Related to NGF and BDNF
Maisonpierre, P. C., Belluscio, L., Squinto, S., Ip, N. Y., Furth, M. E., Lindsay, R. M., & Yancopoulos, G. D. (1990) · Science · doi:10.1126/science.2321006 · Cited by 1,322 · see citing works
Maisonpierre, P. C., Belluscio, L., Friedman, B., Alderson, R. F., Wiegand, S. J., Furth, M. E., Lindsay, R. M., & Yancopoulos, G. D. (1990) · Neuron · doi:10.1016/0896-6273(90)90089-x · Cited by 1,234 · see citing works
Hohn, A., Leibrock, J., Bailey, K., & Barde, Y.-A. (1990) · Nature · doi:10.1038/344339a0 · Cited by 1,145 · see citing works
Ciliary neurotrophic factor prevents the degeneration of motor neurons after axotomy
Sendtner, M., Kreutzberg, G. W., & Thoenen, H. (1990) · Nature · doi:10.1038/345440a0 · Cited by 836 · see citing works
The changing scene of neurotrophic factors
Thoenen, H. (1991) · Trends in Neurosciences · doi:10.1016/0166-2236(91)90097-e · Cited by 820 · see citing works
Potentiation of developing neuromuscular synapses by the neurotrophins NT-3 and BDNF
Lohof, A. M., Ip, N. Y., & Poo, M.-M. (1993) · Nature · doi:10.1038/363350a0 · Cited by 755 · see citing works
Self-citationNeurotrophins promote motor neuron survival and are present in embryonic limb bud
Henderson, C. E., Camu, W., Mettling, C., Gouin, A., Poulsen, K., Karihaloo, M., Ruilamas, J., Evans, T., McMahon, S. B., Armanini, M. P., et al. (1993) · Nature · doi:10.1038/363266a0 · Cited by 608 · see citing works
Arakawa, Y., Sendtner, M., & Thoenen, H. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-11-03507.1990 · Cited by 581 · see citing works
Disruption of the CNTF gene results in motor neuron degeneration
Masu, Y., Wolf, E., Holtmann, B., Sendtner, M., Brem, G., & Thoenen, H. (1993) · Nature · doi:10.1038/365027a0 · Cited by 558 · see citing works
Patterson, S. L., Grover, L. M., Schwartzkroin, P. A., & Bothwell, M. (1992) · Neuron · doi:10.1016/0896-6273(92)90067-n · Cited by 555 · see citing works
Sendtner, M., Schmalbruch, H., Stöckli, K. A., Carroll, P., Kreutzberg, G. W., & Thoenen, H. (1992) · Nature · doi:10.1038/358502a0 · Cited by 551 · see citing works
Ip, N. Y., Stitt, T. N., Tapley, P. M., Klein, R., Glass, D. J., Fandl, J. P., Greene, L. A., Barbacid, M., & Yancopoulos, G. D. (1993) · Neuron · doi:10.1016/0896-6273(93)90306-c · Cited by 514 · see citing works
Control of Embryonic Motoneuron Survival in Vivo by Ciliary Neurotrophic Factor
Oppenheim, R. W., Prevette, D. M., Yin, Q.-W., Collins, F., & MacDonald, J. (1991) · Science · doi:10.1126/science.2011743 · Cited by 447 · see citing works
Interleukin 1β inhibits synaptic strength and long-term potentiation in the rat CA1 hippocampus
Bellinger, F. P., Madamba, S. G., & Siggins, G. R. (1993) · Brain Research · doi:10.1016/0006-8993(93)90959-q · Cited by 388 · see citing works
Synaptic Vesicles and Exocytosis
Jahn, R., & Südhof, T. C. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.001251 · Cited by 383 · see citing works
Sendtner, M., Stöckli, K. A., & Thoenen, H. (1992) · The Journal of Cell Biology · doi:10.1083/jcb.118.1.139 · Cited by 362 · see citing works
Tumor necrosis factor alters synaptic transmission in rat hippocampal slices.
Tancredi, V., D'Arcangelo, G., Grassi, F., Tarroni, P., Palmieri, G., Santoni, A., & Eusebi, F. (1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90071-e · Cited by 326 · see citing works
Regulation of ciliary neurotrophic factor expression in myelin-related Schwann cells in vivo
Friedman, B., Scherer, S. S., Rudge, J. S., Helgren, M. E., Morrisey, D., McClain, J., Wang, D., Wiegand, S. J., Furth, M. E., Lindsay, R. M., et al. (1992) · Neuron · doi:10.1016/0896-6273(92)90168-d · Cited by 307 · see citing works
Neurotrophins promote maturation of developing neuromuscular synapses
Wang, T., Xie, K., & Lu, B. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-07-04796.1995 · Cited by 249 · see citing works
Dounce, A. L., Witter, R. F., Monty, K. J., et al. (1955) · The Journal of Cell Biology · doi:10.1083/jcb.1.2.139 · Cited by 243 · see citing works
Immunolocalization of ciliary neuronotrophic factor in adult rat sciatic nerve
Rende, M., Muir, D. A., Ruoslahti, E. I., et al. (1992) · Glia · doi:10.1002/glia.440050105 · Cited by 166 · see citing works
Gurney, M., Yamamoto, H., & Kwon, Y. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-08-03241.1992 · Cited by 164 · see citing works
Kim, H. G., Wang, T., Olafsson, P., & Lu, B. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.25.12341 · Cited by 161 · see citing works
Heumann, R. (1994) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(94)90008-6 · Cited by 143 · see citing works
Potentiation of transmitter release by ciliary neurotrophic factor requires somatic signaling
Stoop, R., & Poo, M. (1995) · Science · doi:10.1126/science.7839148 · Cited by 136 · see citing works
Self-citationCiliary neurotrophic factor and its receptor complex
Ip, N. Y., & Yancopoulos, G. D. (1992) · Progress in Growth Factor Research · doi:10.1016/0955-2235(92)90028-g · Cited by 125 · see citing works
Ciliary neurotrophic factor maintains motoneurons and their target muscles in developing rats
Forger, N., Roberts, S., Wong, V., et al. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-11-04720.1993 · Cited by 102 · see citing works
Presynaptic Calcium in Transmitter Release and Posttetanic Potentiationa
Zucker, R. S., DEWEY, K. R., Mulkey, R. M., et al. (1991) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1991.tb36492.x · Cited by 98 · see citing works
Magal, E., Burnham, P., & Varon, S. S. (1991) · Developmental Brain Research · doi:10.1016/0165-3806(91)90074-s · Cited by 83 · see citing works
Interleukin-1β increases synaptic inhibition in rat hippocampal pyramidal neurons in vitro
Zeise, M. L., Madamba, S. G., & Siggins, G. R. (1992) · Regulatory Peptides · doi:10.1016/0167-0115(92)90002-c · Cited by 75 · see citing works
Dimaline, R., Vaillant, C., & Dockray, G. J. (1980) · Regulatory Peptides · doi:10.1016/0167-0115(80)90002-6 · Cited by 74 · see citing works
Connolly, J. L., Green, S. A., & Greene, L. (1981) · The Journal of Cell Biology · doi:10.1083/jcb.90.1.176 · Cited by 66 · see citing works
Bindoni, M., Perciavalle, V., Berretta, S., Belluardo, N., & Diamantstein, T. (1988) · Brain Research · doi:10.1016/0006-8993(88)90578-1 · Cited by 66 · see citing works
Thoenen, H., Zafra, F., Hengerer, B., & Lindholm, D. (1991) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1991.tb00196.x · Cited by 61 · see citing works
Abe, K., Xie, F.-J., & Saitō, H. (1991) · Brain Research · doi:10.1016/0006-8993(91)90589-n · Cited by 55 · see citing works
Interferon inhibits synaptic potentiation in rat hippocampus
D’Arcangelo, G., Grassi, F., Ragozzino, D., Santoni, A., Tancredi, V., & Eusebi, F. (1991) · Brain Research · doi:10.1016/0006-8993(91)91459-e · Cited by 55 · see citing works
Nerve-terminal proteins: to fuse to learn
Catsicas, S., Grenningloh, G., & Pich, E. M. (1994) · Trends in Neurosciences · doi:10.1016/0166-2236(94)90045-0 · Cited by 47 · see citing works
Neurotrophic factors and their receptors
Ip, N. Y., & Yancopoulos, G. D. (1994) · Annals of Neurology · doi:10.1002/ana.410350706 · Cited by 47 · see citing works
Tyndall, J. (1870) · Nature · doi:10.1038/001339a0 · Cited by 20 · see citing works
Seifert, W. E., Förster, F. G., Flott, B., et al. (1990) · Advances in experimental medicine and biology · doi:10.1007/978-1-4684-5769-8_43 · Cited by 8 · see citing works
The Veined Structure of Glaciers
Whymper, E. A. D. T. (1870) · Nature · doi:10.1038/001266b0 · Cited by 2 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- Lnhof, A.M. (1994) Modulation of neurite outgrowth and synaptic activity of embryonic Xenopus spinal neurons. Ph.D. Dissertation, Columbia University. New York.
Cited by
Sorted by citations
Nagahara, A. H., Merrill, D. A., Coppola, G., Tsukada, S., Schroeder, B. E., Shaked, G. M., Wang, L., Blesch, A., Kim, A., Conner, J. M., et al. (2009) · Nature Medicine · doi:10.1038/nm.1912 · Cited by 1,034 · see citing works
- Authors
- Stoop, R., & Poo, M.
- Affiliations
- Columbia University (US)
- ORCID
- Venue
- Progress in Brain Research
- Publisher
- Elsevier
- Published
- 1996
- Volume
- 109
- Pages
- 359-364
- ISSN
- 0079-6123 (ISSN-L)
- OpenAlex
- W1621681081
- Cited by
- 47
- References
- 42
- Citations by year
- 2017: 1 · 2016: 1 · 2015: 3 · 2014: 2 · 2012: 3
- FWCI
- 5.51
- Type
- book chapter
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Progress in brain research (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Keywords
- synaptic modulation, neurotrophic factors, neurotrophins, nerve growth factor, ciliary neurotrophic factor, presynaptic neurotransmitter release, synaptic vesicle exocytosis, synapse maturation, neuronal survival
- MeSH terms
- Animals, Brain, Cerebral Cortex, Nerve Growth Factors, Nerve Tissue Proteins, Neuromuscular Junction, Synapses, Long-Term Potentiation, Brain-Derived Neurotrophic Factor, Ciliary Neurotrophic Factor, Rats
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