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Impairment of L-type Ca2+Channel-Dependent Forms of Hippocampal Synaptic Plasticity in Mice Deficient in the Extracellular Matrix Glycoprotein Tenascin-C

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Evers, Matthias R., Salmen, Benedikt, Bukalo, Olena, Rollenhagen, Astrid, Bösl, Michael R., Morellini, Fabio, Bartsch, Udo, Dityatev, Alexander, Schachner, Melitta·2002·The Journal of Neuroscience

DOI 10.1523/jneurosci.22-16-07177.2002PMC PMC6757873

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Abstract

The extracellular matrix glycoprotein tenascin-C (TN-C) has been suggested to play important functional roles during neural development, axonal regeneration, and synaptic plasticity. We generated a constitutively TN-C-deficient mouse mutant from embryonic stem cells with a floxed tn-C allele, representing a standard for future analysis of conditionally targeted mice. The gross morphology of the CNS was not detectably affected, including no evidence for perturbed nerve cell migration, abnormal oligodendrocyte distribution, or defective myelination. Despite the apparent normal histology of the hippocampus and normal performance in the water maze, theta-burst stimulation (TBS) of Schaffer collaterals elicited reduced long-term potentiation (LTP) in the CA1 region of TN-C-deficient mutants, as compared with wild-type littermates. However, high-frequency stimulation evoked normal LTP not only in CA1, but also at mossy fiber-CA3 and medial and lateral perforant path-granule cell synapses in the dentate gyrus. Low-frequency stimulation failed to induce long-term depression in the CA1 region of TN-C-deficient animals. Recordings of TBS-induced LTP in the presence of nifedipine, an antagonist of L-type voltage-dependent Ca2+ channels (VDCCs), did not affect LTP in TN-C-deficient mice, but reduced LTP in wild-type mice to the levels seen in mutants. Furthermore, chemical induction of a L-type VDCC-dependent LTP in the CA1 region by application of the K+ channel blocker tetraethylammonium resulted in impaired LTP in TN-C mutants. Thus, reduction in L-type VDCC-mediated signaling appears to mediate the deficits in certain forms of synaptic plasticity in constitutively TN-C-deficient mice.

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Sambrook, J., Fritsch, E., & Maniatis, T. (1989) · UCLA - Biblioteca de Ciencias de la Salud · Cited by 133,589
Molecular cloning: A laboratory manual
Deininger, P. L. (1990) · Analytical Biochemistry · doi:10.1016/0003-2697(90)90595-z · Cited by 84,684
Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.
Towbin, H., Staehelin, T., & Gordon, J. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.9.4350 · Cited by 53,218
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Place navigation impaired in rats with hippocampal lesions
Morris, R. G. M., Garrud, P., Rawlins, J. N. P., & O'Keefe, J. (1982) · Nature · doi:10.1038/297681a0 · Cited by 6,340
Derivation of completely cell culture-derived mice from early-passage embryonic stem cells.
Nagy, A., Rossant, J., Nagy, R., Abramow-Newerly, W., & Roder, J. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.18.8424 · Cited by 2,328
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Aggleton, J. P., & Brown, M. W. (1999) · Behavioral and Brain Sciences · doi:10.1017/s0140525x99002034 · Cited by 1,879
The essential role of hippocampal CA1 NMDA receptor-dependent synaptic plasticity in spatial memory.
Tsien, J. Z., Huerta, P. T., & Tonegawa, S. (1996) · Cell · doi:10.1016/s0092-8674(00)81827-9 · Cited by 1,782 · cited 2×
“Particularly, levels of NMDA receptordependent LTP at Schaffer collateral-A1 synapses have been correlated with performance in certain tests of spatial learning and memory (Tsien et al., 1996; Shimizu et al., 2000; Zeng et al., 2001).”
BackgroundMethod
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Gu, H., Marth, J. D., Orban, P. C., Mossmann, H., & Rajewsky, K. (1994) · Science · doi:10.1126/science.8016642 · Cited by 1,397
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Show all 81 references

Research works printed but not linked: 1

Faissner A, Schachner M (1995) Tenascin and janusin: Glial recognition molecules involved in neural development and regeneration. In: Neu- roglia (Kettenmann H, Ransom BR, eds), pp 422-426. New York: Oxford University Press.

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Authors: Evers, M. R., Salmen, B., Bukalo, O., Rollenhagen, A., Bösl, M. R., Morellini, F., Bartsch, U., Dityatev, A., & Schachner, M.
Affiliations: Universität Hamburg (DE)
ORCID: Bukalo, Olena
Rollenhagen, Astrid
Morellini, Fabio
Bartsch, Udo
Dityatev, Alexander
Schachner, Melitta
Venue: The Journal of Neuroscience
Publisher: Society for Neuroscience
Published: 2002-08-15
Volume: 22
Issue: 16
Pages: 7177-7194
ISSN: 0270-6474 (ISSN-L)
1529-2401
DOI: 10.1523/jneurosci.22-16-07177.2002
PMC: PMC6757873
OpenAlex: W2141616957
Cited by: 172
References: 81
Citations by year: 2026: 4 · 2025: 6 · 2024: 5 · 2023: 5 · 2022: 9 · 2021: 8 · 2020: 3 · 2019: 3 · 2018: 9 · 2017: 7 · 2016: 7 · 2015: 4 · 2014: 9 · 2013: 6 · 2012: 10
FWCI: 3.38
Type: journal article
Language: en
Open access: bronze
doi.org
Locations: Journal of Neuroscience (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Rutgers University Community Repository (Rutgers University) (submittedVersion)
Funders: Deutsche Forschungsgemeinschaft
Rheinische Friedrich-Wilhelms-Universität Bonn
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Keywords: tenascin-C, extracellular matrix, L-type calcium channels, hippocampal synaptic plasticity, long-term potentiation, long-term depression, CA1 region, dentate gyrus, Schaffer collaterals, perforant path, tetraethylammonium, nifedipine, floxed allele
MeSH terms: Animals, Behavior, Animal, Cerebellar Cortex, Electric Stimulation, Hippocampus, Male, Neural Inhibition, Neuronal Plasticity, Neurons, Optic Nerve, Retina, Synapses, Blotting, Western, Long-Term Potentiation, Mice, Knockout, Gene Targeting, Excitatory Amino Acid Antagonists, Maze Learning, Tenascin, Excitatory Postsynaptic Potentials, Calcium Channels, L-Type, Mice, In Vitro Techniques

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Impairment of L-type Ca2+Channel-Dependent Forms of Hippocampal Synaptic Plasticity in Mice Deficient in the Extracellular Matrix Glycoprotein Tenascin-C

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