Cortical sources of CRF, NKB, and CCK and their effects on pyramidal cells in the neocortex
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In order to investigate how neuropeptide transmission can modulate the neocortical network, we mapped the expression of neurokinin (NK) B, cholecystokinin (CCK), and corticotropin-releasing factor (CRF) and their receptors to neuronal types using patch-clamp and single-cell reverse transcription-polymerase chain reaction in acute slices of rat neocortex. Classification of neurons by unsupervised clustering based on the analysis of multiple electrophysiological and molecular properties disclosed 3 GABAergic interneuron clusters and 1 pyramidal cell cluster. The 3 neuropeptides were expressed in a cluster of interneurons characteristically expressing vasoactive intestinal peptide. CRF was additionally found in a cluster containing almost exclusively somatostatin-expressing interneurons, whereas CCK was present in all clusters. The respective receptors of these peptides, NK-3, CCK-B, and CRF-1, were essentially expressed in pyramidal cells. At -60 mV, pyramidal cells were weakly depolarized by each of these peptides. When pyramidal neurons were maintained to about 5 mV below spike threshold, depolarization induced by each peptide resulted in a long-lasting action potential discharge. Neuropeptide effects were prevented by selective antagonists of NK-3, CCK-B, and CRF-1 receptors. These results suggest that pyramidal neurons are the primary target of NKB, CCK, and CRF in the neocortex. They further indicate that specific interneuron types coordinate the release of these peptides and can induce a long-lasting increase of the excitability of the neocortical network.
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Published physiological results on cortical neuropeptide signaling are surprisingly rare given the breadth of neuroscientific interest in cortex.
“published physiological results are surprisingly rare given the breadth of neuroscientific interest in cortex.”
From Single-cell transcriptomic evidence for dense intracortical neuropeptide networks (2019) · cites this paper as Gallopin et al., 2006
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Karagiannis, A., Gallopin, T., Dávid, C., Battaglia, D., Geoffroy, H., Rossier, J., Hillman, E. M. C., Staiger, J. F., & Cauli, B. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.0058-09.2009 · Cited by 256 · see citing works
Self-citationKubota, Y., Shigematsu, N., Karube, F., Sekigawa, A., Kato, S., Yamaguchi, N., Hirai, Y., Morishima, M., & Kawaguchi, Y. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq252 · Cited by 235 · see citing works
Single-cell transcriptomic evidence for dense intracortical neuropeptide networks
Smith, S. J., Sümbül, U., Graybuck, L. T., Collman, F., Seshamani, S., Gala, R., Gliko, O., Elabbady, L., Miller, J. A., Bakken, T. E., et al. (2019) · eLife · doi:10.7554/elife.47889 · Cited by 156 · see citing works
Self-citationVucurovic, K., Gallopin, T., Ferezou, I., Rancillac, A., Chameau, P., van Hooft, J. A., Geoffroy, H., Monyer, H., Rossier, J., & Vitalis, T. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhp310 · Cited by 139 · see citing works
Self-citationComparative density of CCK- and PV-GABA cells within the cortex and hippocampus
Whissell, P. D., Cajanding, J. D., Fogel, N., & Kim, J. C. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00124 · Cited by 118 · see citing works
Revisiting enigmatic cortical calretinin-expressing interneurons
Cauli, B., Zhou, X., Tricoire, L., Toussay, X., & Staiger, J. F. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00052 · Cited by 86 · see citing works
Glutamate receptors of the delta family are widely expressed in the adult brain
Hepp, R., Hay, Y. A., Aguado, C., Lujan, R., Dauphinot, L., Potier, M. C., Nomura, S., Poirel, O., El Mestikawy, S., Lambolez, B., et al. (2015) · Brain Structure and Function · doi:10.1007/s00429-014-0827-4 · Cited by 71 · see citing works
Self-citationExtensive overlap of mu-opioid and nicotinic sensitivity in cortical interneurons
Ferezou, I., Hill, E. L., Cauli, B., Gibelin, N., Kaneko, T., Rossier, J., & Lambolez, B. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhl104 · Cited by 65 · see citing works
Patel, R. R., Wolfe, S. A., Borgonetti, V., Gandhi, P. J., Rodriguez, L., Snyder, A. E., D’Ambrosio, S., Bajo, M., Domissy, A., Head, S., et al. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01642-3 · Cited by 33 · see citing works
New light on cortical neuropeptides and synaptic network plasticity
Smith, S. J., Hawrylycz, M., Rossier, J., & Sümbül, U. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.04.002 · Cited by 26 · see citing works
Self-citation
- Authors
- Gallopin, T., Geoffroy, H., Rossier, J., & Lambolez, B.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- Corresponding author
- Gallopin, Thierry
- Venue
- Cerebral Cortex
- Publisher
- Oxford University Press (OUP)
- Published
- 2005-12-07
- Volume
- 16
- Issue
- 10
- Pages
- 1440-1452
- ISSN
- 1047-3211 (ISSN-L)
- 1460-2199
- OpenAlex
- W2146748168
- Cited by
- 97
- References
- 109
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 2 · 2023: 7 · 2022: 6 · 2021: 6 · 2020: 5 · 2019: 3 · 2018: 5 · 2017: 3 · 2016: 3 · 2015: 6 · 2014: 10 · 2013: 5 · 2012: 5
- FWCI
- 0.84
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- other-oa
- Locations
- Cerebral Cortex (publishedVersion, other-oa)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- corticotropin-releasing factor, neurokinin B, cholecystokinin, neuropeptide receptors, neocortical pyramidal cells, GABAergic interneurons, vasoactive intestinal peptide, somatostatin, NK3 receptor, CCK-B receptor, neuronal excitability, receptor antagonists
- MeSH terms
- Action Potentials, Animals, Cells, Cultured, Cholecystokinin, Corticotropin-Releasing Hormone, Synaptic Transmission, Tissue Distribution, Neurokinin B, Rats, Wistar, Pyramidal Cells, Neurotransmitter Agents, Neocortex, Rats
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