Evidence map›Paper›PMID 40560417›Full record

ArticlePflugers Archiv : European journal of physiology2025

Presynaptic maturation of inhibitory connections onto vasoactive intestinal polypeptide-expressing GABAergic interneurons in the mouse barrel field.

Clara A Simacek, Sergei Kirischuk, Thomas Mittmann

Abstract read
In one paragraph

Article in Pflugers Archiv : European journal of physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Clara A SimacekInstitute for Physiology, University Medical Centre of the Johannes Gutenberg University Mainz, Mainz, Germany.ORCID 0009-0003-6843-0760
Sergei KirischukInstitute for Physiology, University Medical Centre of the Johannes Gutenberg University Mainz, Mainz, Germany.ORCID 0000-0003-2465-5864
Thomas MittmannInstitute for Physiology, University Medical Centre of the Johannes Gutenberg University Mainz, Mainz, Germany. mittmann@uni-mainz.de.ORCID 0000-0001-6002-2963

Funding

Deutsche Forschungsgemeinschaft CRC 1080 C02
6 · The paper itself

Abstract

Vasoactive intestinal polypeptide-expressing inhibitory interneurons (VIP-INs) in the adult barrel cortex are crucial for mediating active whisking (AW) by disinhibiting pyramidal neurons. Past studies have investigated the development of VIP-IN network integration, focusing mainly on the excitatory network or the postsynaptic side of the inhibitory network. Hence, we aimed to explore the inhibitory network integration of VIP-INs, concentrating on the presynaptic side. We addressed this by investigating VIP-INs in three different age groups (postnatal day (P)8-P10, P14-P16, and P30-P36) in Vip-IRES-cre x tdTomato mice with whole-cell patch clamp recordings. By placing a stimulation electrode into L4 of the barrel field, we elicited electrically-evoked inhibitory postsynaptic currents (eIPSCs) in L2/3 VIP-INs following a high-frequency stimulation. We then analysed recorded eIPSCs by applying the binomial model of synaptic transmission. Our results show significant increases in both the number of readily-releasable vesicles and the presynaptic release probability between P9 and P15, suggesting that the inhibitory network integration is at least partially conducted via a presynaptic functional maturation. Despite an increase in the release probability, synaptic depression is decreased at P30-P36 due to an accelerated vesicle replenishment rate within the same time window. Lastly, asynchronous vesicle release decreases in favour of a stimulus-locked signal transmission by P30-P36. Our results suggest a maturation of the inhibitory projections towards a strong, precise, and stimulus-locked inhibition. This can be physiologically relevant to define the temporal precision of AW at the relevant frequencies.

Indexed as

GABAergic NeuronsInterneuronsPresynaptic TerminalsSomatosensory CortexVasoactive Intestinal PeptideAnimalsInhibitory Postsynaptic PotentialsMaleMiceMice, Inbred C57BLNeural InhibitionSynaptic TransmissionVibrissaeVasoactive Intestinal PeptideDevelopmentInhibitionInterneuronQuantal analysisSomatosensoryVIP

Identifiers

PMID40560417
PMCPMC12310910

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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.