Layer I Interneurons Sharpen Sensory Maps during Neonatal Development
Open accessAbstract
The neonatal mammal faces an array of sensory stimuli when diverse neuronal types have yet to form sensory maps. How these inputs interact with intrinsic neuronal activity to facilitate circuit assembly is not well understood. By using longitudinal calcium imaging in unanesthetized mouse pups, we show that layer I (LI) interneurons, delineated by co-expression of the 5HT3a serotonin receptor (5HT3aR) and reelin (Re), display spontaneous calcium transients with the highest degree of synchrony among cell types present in the superficial barrel cortex at postnatal day 6 (P6). 5HT3aR Re interneurons are activated by whisker stimulation during this period, and sensory deprivation induces decorrelation of their activity. Moreover, attenuation of thalamic inputs through knockdown of NMDA receptors (NMDARs) in these interneurons results in expansion of whisker responses, aberrant barrel map formation, and deficits in whisker-dependent behavior. These results indicate that recruitment of specific interneuron types during development is critical for adult somatosensory function. VIDEO ABSTRACT.
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Inhibition is likely stronger on weakly activated layer 2/3 pyramidal cells above septa than above barrels, which would help form barrel columns tuned to individual whiskers.
“Inhibition is likely more prominent on weakly activated layer 2/3 pyramidal cells immediately above septal regions than in layer 2/3 pyramidal cells above the barrels (where VPM axons concentrate), which would contribute to the formation of barrel columns tuned to individual whiskers (Che et al., 2018).”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Che et al., 2018
Neurogliaform cell activity during this period inhibits layer 2/3 pyramidal cell responses during whisker stimulation.
“The activity of neurogliaform cells during this period inhibits the response of layer 2/3 pyramidal cells during whisker stimulation.”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Che et al., 2018
During the first postnatal week, activity of layer 1 5HT3aR+ interneurons, mostly neurogliaform cells, in the barrel field is highly synchronized by VPM thalamic inputs and requires NMDAR function.
“During the first week of postnatal development, the activity of layer 1 5HT3aR+ interneurons (mostly neurogliaform cells) in the barrel field is highly synchronized by inputs from the somatosensory thalamus (ventroposteromedial thalamic nucleus, VPM), a process that requires NMDAR function (Che et al., 2018).”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Che et al., 2018
Activation of layer 1 neurogliaform cells by thalamic input is transient, like the temporary recruitment of deep layer SST+ interneurons.
“Intriguingly, the activation of layer 1 neurogliaform cells by thalamic input is transient, much like the temporary recruitment of deep layer SST+ interneurons (Che et al., 2018).”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Che et al., 2018
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Quast, K. B., Ung, K., Froudarakis, E., Huang, L., Herman, I., Addison, A. P., Ortiz‐Guzman, J., Cordiner, K., Saggau, P., Tolias, A. S., et al. (2016) · Nature Neuroscience · doi:10.1038/nn.4467 · Cited by 41 · see citing works
Electrical coupling regulates layer 1 interneuron microcircuit formation in the neocortex
Yao, X.-H., Wang, M., He, X.-N., He, F., Zhang, S.-Q., Lu, W., Qiu, Z., & Yu, Y. (2016) · Nature Communications · doi:10.1038/ncomms12229 · Cited by 36 · see citing works
Che, A., Truong, D. T., FITCH, R. H., & LoTurco, J. J. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv168 · Cited by 27 · see citing works
Self-citationSubtype-selective Electroporation of Cortical Interneurons
García, N. V. D. M., & Fishell, G. (2014) · Journal of Visualized Experiments · doi:10.3791/51518 · Cited by 13 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Development and Functional Diversification of Cortical Interneurons
Lim, L., Mi, D., Llorca, A., & Marín, O. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.009 · Cited by 714 · see citing works
Prefrontal Cortex Development in Health and Disease: Lessons from Rodents and Humans
Chini, M., & Hanganu-Opatz, I. L. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2020.10.017 · Cited by 253 · see citing works
GABAergic Restriction of Network Dynamics Regulates Interneuron Survival in the Developing Cortex
Duan, Z. R. S., Che, A., Chu, P., Modol, L., Bollmann, Y., Babij, R., Fetcho, R. N., Otsuka, T., Fuccillo, M. V., Liston, C., et al. (2020) · Neuron · doi:10.1016/j.neuron.2019.10.008 · Cited by 102 · see citing works
Self-citation
- Authors
- Che, A., Babij, R., Iannone, A. F., Fetcho, R. N., Ferrer, M., Liston, C., Fishell, G., & De Marco García, N. V.
- Affiliations
- Weill Cornell Medicine (US)
- Cornell University (US)
- Harvard University (US)
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2018-07
- Volume
- 99
- Issue
- 1
- Pages
- 98-116.e7
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC6152945
- OpenAlex
- W2809648019
- Cited by
- 91
- References
- 96
- Citations by year
- 2026: 4 · 2025: 13 · 2024: 13 · 2023: 12 · 2022: 16 · 2021: 15 · 2020: 13 · 2019: 4 · 2018: 1
- FWCI
- 3.04
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- NIH
- NIMH (1R01MH110553-01, 1R01 MH109685)
- Citizens United for Research in Epilepsy
- Leon Levy Foundation
- Frueauff Foundation
- NIGMS (T32GM007739)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Tactile and Sensory Interactions
- Keywords
- barrel cortex, neonatal development, reelin, spontaneous calcium transients, neuronal synchronization, whisker stimulation, sensory deprivation, thalamic input, somatosensory development, mouse pups
- MeSH terms
- Reelin Protein, Animals, Animals, Newborn, Calcium, Cerebral Cortex, Interneurons, Nerve Tissue Proteins, Neural Pathways, Physical Stimulation, Sensory Deprivation, Serine Endopeptidases, Somatosensory Cortex, Touch, Vibrissae, Cell Adhesion Molecules, Neuronal, Receptors, N-Methyl-D-Aspartate, Extracellular Matrix Proteins, Pyramidal Cells, Patch-Clamp Techniques, Receptors, Serotonin, 5-HT3, Mice, Gene Knockdown Techniques, Optogenetics
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.
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