Target-Specific Properties of Thalamocortical Synapses onto Layer 4 of Mouse Primary Visual Cortex
Open accessAbstract
In primary sensory cortices, thalamocortical (TC) inputs can directly activate excitatory and inhibitory neurons. In vivo experiments in the main input layer (L4) of primary visual cortex (V1) have shown that excitatory and inhibitory neurons have different tuning properties. The different functional properties may arise from distinct intrinsic properties of L4 neurons, but could also depend on cell type-specific properties of the synaptic inputs from the lateral geniculate nucleus of the thalamus (LGN) onto L4 neurons. While anatomical studies identified LGN inputs onto both excitatory and inhibitory neurons in V1, their synaptic properties have not been investigated. Here we used an optogenetic approach to selectively activate LGN terminal fields in acute coronal slices containing V1, and recorded monosynaptic currents from excitatory and inhibitory neurons in L4. LGN afferents made monosynaptic connections with pyramidal (Pyr) and fast-spiking (FS) neurons. TC EPSCs on FS neurons were larger and showed steeper short-term depression in response to repetitive stimulation than those on Pyr neurons. LGN inputs onto Pyr and FS neurons also differed in postsynaptic receptor composition and organization of presynaptic release sites. Together, our results demonstrate that LGN input onto L4 neurons in mouse V1 have target-specific presynaptic and postsynaptic properties. Distinct mechanisms of activation of feedforward excitatory and inhibitory neurons in the main input layer of V1 are likely to endow neurons with different response properties to incoming visual stimuli.
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The core features of thalamocortical feedforward inhibition are present and at least qualitatively similar in other sensory modalities and species.
“it seems that its core features are also present and are at least qualitatively similar in other sensory modalities such as vision and audition as well as in other species (Kloc and Maffei, 2014; Miller et al., 2001; Schiff and Reyes, 2012).”
From GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits (2016) · cites this paper as Kloc and Maffei, 2014
PV+ FS interneurons receive strong thalamic inputs while SOM+ non-FS interneurons receive weaker thalamic inputs.
“For example, PV+ FS interneurons receive strong thalamic inputs16–20 while SOM+ non-FS interneurons receive weaker thalamic inputs21,22.”
From Layer 4 of mouse neocortex differs in cell types and circuit organization between sensory areas (2019) · cites this paper as [20]
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References 80 · Cited by 99
- Authors
- Kloc, M., & Maffei, A.
- Affiliations
- Stony Brook University (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2014-11-12
- Volume
- 34
- Issue
- 46
- Pages
- 15455-15465
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6608443
- OpenAlex
- W2145085279
- Cited by
- 99
- References
- 80
- Citations by year
- 2026: 8 · 2025: 7 · 2024: 2 · 2023: 6 · 2022: 6 · 2021: 7 · 2020: 11 · 2019: 9 · 2018: 10 · 2017: 12 · 2016: 13 · 2015: 8
- FWCI
- 5.03
- 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)
- Funders
- Whitehall Foundation
- National Eye Institute (R01EY019885)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- thalamocortical synapses, primary visual cortex, layer 4, lateral geniculate nucleus, fast-spiking interneurons, pyramidal neurons, short-term depression, presynaptic release sites, feedforward inhibition, mice
- MeSH terms
- Animals, Female, Geniculate Bodies, Male, Neurons, Synapses, Visual Cortex, Pyramidal Cells, Excitatory Postsynaptic Potentials, Mice, Optogenetics, In Vitro Techniques
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