Evidence map›Paper›PMID 41190957›Full record

ArticleThe Journal of comparative neurology2025

Differences in Cajal-Retzius Cell Density and Postnatal Persistence Across Cortical Areas Revealed by a Novel Intersectional Genetic Labeling Approach.

Kristian Moan, Robert Machold, Giulia Quattrocolo

Abstract read
In one paragraph

Article in The Journal of comparative neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

3 authors.

Kristian MoanKavli Institute for Systems Neuroscience and Centre for Algorithms in the Cortex, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.ORCID 0009-0005-5105-5444
Robert MacholdNeuroscience Institute, New York University Grossman School of Medicine, New York, New York, USA.
Giulia QuattrocoloKavli Institute for Systems Neuroscience and Centre for Algorithms in the Cortex, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.ORCID 0000-0001-6508-8910

Funding

Brain and Behavior Research Foundation 31551Kavli FoundationNorges Forskningsråd 223262Norges Forskningsråd 295721Norges Forskningsråd 324305Norges Forskningsråd 332640
6 · The paper itself

Abstract

Cajal-Retzius (CR) cells are glutamatergic neurons that transiently populate the most superficial layer of the isocortex and allocortex during development, serving an essential role during both prenatal and early postnatal brain development. Notably, these cells disappear from most cortical areas by postnatal day 14 but persist for much longer in the hippocampus. We developed a novel intersectional genetic labeling approach for CR cells that captures almost all of the TRP73-positive CR cells throughout the isocortex and allocortex. This intersectional strategy offers several advantages over previous methods commonly used for CR cell targeting. Here, we applied this new CR cell-labeling strategy to investigate the distribution and persistence of CR cells throughout the whole mouse brain at four different postnatal ages. We observed that the initial CR cell density and the rate of their disappearance vary substantially across different brain areas during development. Strikingly, we observed variation in cell death rate even between adjacent cortical subregions: comparing the medial and the lateral entorhinal cortex, the former retains a high density of CR cells for several months in contrast to the latter. Our results present a necessary revision of the phenomenon of CR cell persistence, showing that, in addition to the hippocampus, several other cortical areas maintain a high density of these cells beyond the first 2 postnatal weeks.

Indexed as

Cerebral CortexNeuronsAnimalsAnimals, NewbornCell CountFemaleMaleMiceMice, Inbred C57BLMice, TransgenicCajal–Retzius cellsdevelopmententorhinal cortexhippocampus

Identifiers

PMID41190957
PMCPMC12588112

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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.