Evidence map›Paper›PMID 33531369›Full record

ArticleeNeuro

Parvalbumin Interneurons Are Differentially Connected to Principal Cells in Inhibitory Feedback Microcircuits along the Dorsoventral Axis of the Medial Entorhinal Cortex.

Sabine Grosser, Federico J Barreda, Prateep Beed, Dietmar Schmitz, Sam A Booker, Imre Vida

Open access · goldAbstract read
In one paragraph

Article in eNeuro. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Cortical control of chandelier cells in neural codes.Frontiers in cellular neuroscience · 2022
    Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 5 institutions in 4 countries.

Sabine GrosserInstitute for Integrative Neuroanatomy, Charité - Universitätsmedizin Berlin, Berlin 10117, Germany.
Federico J BarredaInstitute for Integrative Neuroanatomy, Charité - Universitätsmedizin Berlin, Berlin 10117, Germany.
Prateep BeedNeurowissenschaftliches Forschungszentrum, Charité-Universitätsmedizin, Berlin 10117, Germany.
Dietmar SchmitzBerlin Institute of Health, Berlin 10178, Germany.
Sam A BookerInstitute for Integrative Neuroanatomy, Charité - Universitätsmedizin Berlin, Berlin 10117, Germany imre.vida@charite.de sbooker@ed.ac.uk.ORCID 0000-0003-1980-9873
Imre VidaInstitute for Integrative Neuroanatomy, Charité - Universitätsmedizin Berlin, Berlin 10117, Germany imre.vida@charite.de sbooker@ed.ac.uk.ORCID 0000-0003-3214-2233
Charité - Universitätsmedizin Berlin · DEBerlin Institute of Health at Charité - Universitätsmedizin Berlin · DEBernstein Center for Computational Neuroscience Berlin · DEDiscovery Centre · CAGerman Center for Neurodegenerative Diseases · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The medial entorhinal cortex (mEC) shows a high degree of spatial tuning, predominantly grid cell activity, which is reliant on robust, dynamic inhibition provided by local interneurons (INs). In fact, feedback inhibitory microcircuits involving fast-spiking parvalbumin (PV) basket cells (BCs) are believed to contribute dominantly to the emergence of grid cell firing in principal cells (PrCs). However, the strength of PV BC-mediated inhibition onto PrCs is not uniform in this region, but high in the dorsal and weak in the ventral mEC. This is in good correlation with divergent grid field sizes, but the underlying morphologic and physiological mechanisms remain unknown. In this study, we examined PV BCs in layer (L)2/3 of the mEC characterizing their intrinsic physiology, morphology and synaptic connectivity in the juvenile rat. We show that while intrinsic physiology and morphology are broadly similar over the dorsoventral axis, PV BCs form more connections onto local PrCs in the dorsal mEC, independent of target cell type. In turn, the major PrC subtypes, pyramidal cell (PC) and stellate cell (SC), form connections onto PV BCs with lower, but equal probability. These data thus identify inhibitory connectivity as source of the gradient of inhibition, plausibly explaining divergent grid field formation along this dorsoventral axis of the mEC.

Indexed as

Entorhinal CortexParvalbuminsAction PotentialsAnimalsFeedbackInterneuronsPyramidal CellsRatsParvalbuminsentorhinal cortexfeedback inhibitionGABAergic interneuronsmicrocircuitmorphologysynapse

Identifiers

PMID33531369
PMCPMC8114875
OpenAlexW3127890399

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.