Evidence map›Paper›PMID 25253849›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Optogenetic activation of cajal-retzius cells reveals their glutamatergic output and a novel feedforward circuit in the developing mouse hippocampus.

Giulia Quattrocolo, Gianmaria Maccaferri

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.1field-weighted citation impact, top 15% 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

26 citing papers in PubMed, 48 citations in OpenAlex.

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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

2 authors at 1 institution in 1 country.

Giulia QuattrocoloDepartment of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611.
Gianmaria MaccaferriDepartment of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611 g-maccaferri@northwestern.edu.
Northwestern University · US

Funding

Cajal-Retzius Cells and Neuronal Signaling in Postnatal Cortical NetworksR01NS064135 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MACCAFERRI, GIANMARIA · 2010 to 2023
$5.3M
NINDS NIH HHS NS 064135NINDS NIH HHS R01 NS064135
6 · The paper itself

Abstract

Cajal-Retzius cells orchestrate the development of cortical circuits by secreting the glycoprotein reelin. However, their computational functions are still unknown. In fact, the nature of their postsynaptic targets, major neurotransmitter released, as well as the class of postsynaptic receptors activated by their firing remain unclear. Here, we have addressed these questions by activating Cajal-Retzius cells optogenetically in mouse hippocampal slices. Light delivered to stratum lacunosum-moleculare triggered EPSCs both on local interneurons and on pyramidal cells. Responses recorded under voltage-clamp conditions had identical short latencies and similar amplitudes, but were kinetically different (i.e., faster in interneurons vs pyramidal cells). In both cases, responses were blocked by TTX, indicating that they were generated by action potential-dependent release. Responses in interneurons were rescued by the addition of 4-AP to TTX, and decreased when presynaptic firing in Cajal-Retzius cells was reduced by the chemokine CXCL12, indicating the existence of a direct Cajal-Retzius cell-interneuron monosynaptic connection. Although the combined application of 4-AP and TTX did not rescue responses in pyramidal cells, neither were they affected by the GABAA receptor blocker gabazine, which would be expected if they were polysynaptic. Both connections showed physiological and pharmacological properties indicating the involvement of AMPA- and NMDA-type glutamate receptors. The connectivity from presynaptic Cajal-Retzius cells to interneurons was strong enough to generate long-latency feedforward GABAergic input onto pyramidal cells. We propose that this newly defined Cajal-Retzius cell-dependent microcircuit may regulate synaptic plasticity and dendritic development in stratum lacunosum-moleculare, thus impacting the integrative properties of the developing hippocampus.

Indexed as

Excitatory Postsynaptic Potentials4-AminopyridineAnimalsChemokine CXCL12Feedback, PhysiologicalFemaleGABA-A Receptor AntagonistsGABAergic NeuronsGlutamic AcidHippocampusInterneuronsMaleMiceMice, Inbred StrainsOptogeneticsPotassium Channel Blockers4-AminopyridineChemokine CXCL12GABA-A Receptor AntagonistsgabazineGlutamic AcidPotassium Channel BlockersPyridazinesReelin ProteinReln protein, mouseSodium Channel BlockersTetrodotoxinAMPA receptorchemokineGABAA receptorglutamateinterneuronNMDA receptor

Identifiers

PMID25253849
PMCPMC4172799
OpenAlexW2046375005

What OpenQuestion holds

Textmetadata
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.