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Dense, Unspecific Connectivity of Neocortical Parvalbumin-Positive Interneurons: A Canonical Microcircuit for Inhibition?
Open accessAbstract
GABAergic interneurons play a major role in the function of the mammalian neocortex, but their circuit connectivity is still poorly understood. We used two-photon RuBi-Glutamate uncaging to optically map how the largest population of cortical interneurons, the parvalbumin-positive cells (PV+), are connected to pyramidal cells (PCs) in mouse neocortex. We found locally dense connectivity from PV+ interneurons onto PCs across cortical areas and layers. In many experiments, all nearby PV+ cells were connected to every local PC sampled. In agreement with this, we found no evidence for connection specificity, as PV+ interneurons contacted PC pairs similarly regardless of whether they were synaptically connected or not. We conclude that the microcircuit architecture for PV+ interneurons, and probably neocortical inhibition in general, is an unspecific, densely homogenous matrix covering all nearby pyramidal cells.
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In the citing paper
“Individual PV-INs contact nearly every local pyramidal neuron which enables them to synchronize networks [74].”
From Parvalbumin interneuron vulnerability and brain disorders (2021) · cites this paper as [74]
In the citing paper
“In addition, PV-INs connect to many principal neurons [74,75,87,88].”
From Parvalbumin interneuron vulnerability and brain disorders (2021) · cites this paper as [74]
In the citing paper
“Some subtypes, such as PVBCs and NGFCs, demonstrate very high rates of connectivity to PCs: connection probabilities in paired recordings are in the range of ~50–90% (204, 331, 876, 880).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [876]
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“However, recent evidence suggests that certain forms of inhibition are promiscuous and less selective in downstream targeting than initially thought (331, 552, 876, 918).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [876]
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Metadata
- Authors
- Packer, A. M., & Yuste, R.
- Affiliations
- Howard Hughes Medical Institute (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2011-09-14
- Volume
- 31
- Issue
- 37
- Pages
- 13260-13271
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC3178964
- OpenAlex
- W2014350866
- Cited by
- 506
- References
- 45
- Citations by year
- 2026: 15 · 2025: 29 · 2024: 53 · 2023: 31 · 2022: 36 · 2021: 43 · 2020: 40 · 2019: 34 · 2018: 30 · 2017: 35 · 2016: 35 · 2015: 35 · 2014: 26 · 2013: 42 · 2012: 16
- FWCI
- 11.82
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- parvalbumin interneurons, GABAergic interneurons, neocortex, pyramidal neurons, cortical connectivity, inhibitory microcircuits, dense connections, glutamate uncaging, two-photon calcium imaging, mouse cortex
- MeSH terms
- Animals, Brain Mapping, Female, Interneurons, Male, Mice, Transgenic, Neural Inhibition, Neural Pathways, Parvalbumins, Pyramidal Cells, Patch-Clamp Techniques, Microscopy, Confocal, Neocortex, Mice, In Vitro Techniques
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