Evidence map›Paper›PMID 32572071›Full record

ArticleScientific reports2020

LTP of inhibition at PV interneuron output synapses requires developmental BMP signaling.

Evan Vickers, Denys Osypenko, Christopher Clark, Zeynep Okur, Peter Scheiffele, Ralf Schneggenburger

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 54% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Dysregulation of BMP, Wnt, and Insulin Signaling in Fragile X Syndrome.Frontiers in cell and developmental biology · 2022
    Review
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 3 institutions in 2 countries.

Evan VickersLaboratory of Synaptic Mechanisms, Brain Mind Institute, School of Life Science, École Polytechnique Fédérale de Lausanne (EPFL), 1015, Lausanne, Switzerland.
Denys OsypenkoLaboratory of Synaptic Mechanisms, Brain Mind Institute, School of Life Science, École Polytechnique Fédérale de Lausanne (EPFL), 1015, Lausanne, Switzerland.
Christopher ClarkLaboratory of Synaptic Mechanisms, Brain Mind Institute, School of Life Science, École Polytechnique Fédérale de Lausanne (EPFL), 1015, Lausanne, Switzerland.
Zeynep OkurBiozentrum, University of Basel, 4056, Basel, Switzerland.
Peter ScheiffeleBiozentrum, University of Basel, 4056, Basel, Switzerland.
Ralf SchneggenburgerLaboratory of Synaptic Mechanisms, Brain Mind Institute, School of Life Science, École Polytechnique Fédérale de Lausanne (EPFL), 1015, Lausanne, Switzerland. ralf.schneggenburger@epfl.ch.
École Polytechnique Fédérale de Lausanne · CHUniversity of Basel · CHSwiss Institute for Regenerative Medicine · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parvalbumin (PV)-expressing interneurons (PV-INs) mediate well-timed inhibition of cortical principal neurons, and plasticity of these interneurons is involved in map remodeling of primary sensory cortices during critical periods of development. To assess whether bone morphogenetic protein (BMP) signaling contributes to the developmental acquisition of the synapse- and plasticity properties of PV-INs, we investigated conditional/conventional double KO mice of BMP-receptor 1a (BMPR1a; targeted to PV-INs) and 1b (BMPR1a/1b (c)DKO mice). We report that spike-timing dependent LTP at the synapse between PV-INs and principal neurons of layer 4 in the auditory cortex was absent, concomitant with a decreased paired-pulse ratio (PPR). On the other hand, baseline synaptic transmission at this connection, and action potential (AP) firing rates of PV-INs were unchanged. To explore possible gene expression targets of BMP signaling, we measured the mRNA levels of the BDNF receptor TrkB and of P/Q-type Ca

Indexed as

AnimalsAuditory CortexBone Morphogenetic Protein Receptors, Type IFemaleGene Knockout TechniquesInterneuronsLong-Term PotentiationMaleMatrix MetalloproteinasesMiceParvalbuminsSignal TransductionBmpr1a protein, mouseBmpr1b protein, mouseBone Morphogenetic Protein Receptors, Type IMatrix MetalloproteinasesParvalbumins

Identifiers

PMID32572071
PMCPMC7308402
OpenAlexW3035939666

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.