Evidence map›Paper›PMID 26189100›Full record

ArticleBrain structure & function2016

Radial and tangential migration of telencephalic somatostatin neurons originated from the mouse diagonal area.

Luis Puelles, N Morales-Delgado, P Merchán, B Castro-Robles, M Martínez-de-la-Torre, C Díaz, J L Ferran

Open access · hybridAbstract read
In one paragraph

Article in Brain structure & function, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

32 citing papers in PubMed, 55 citations in OpenAlex.

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  10. Single cell enhancer activity distinguishes GABAergic and cholinergic lineages in embryonic mouse basal ganglia.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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

7 authors at 3 institutions in 2 countries.

Luis PuellesDepartment of Human Anatomy and Psychobiology, School of Medicine, University of Murcia, Murcia, E30071, Spain. puelles@um.es.
N Morales-DelgadoDepartment of Human Anatomy and Psychobiology, School of Medicine, University of Murcia, Murcia, E30071, Spain.
P MerchánDepartment of Human Anatomy and Psychobiology, School of Medicine, University of Murcia, Murcia, E30071, Spain.
B Castro-RoblesDepartment of Medical Sciences, School of Medicine, University of Castilla-La Mancha, Albacete, E02006, Spain.
M Martínez-de-la-TorreDepartment of Human Anatomy and Psychobiology, School of Medicine, University of Murcia, Murcia, E30071, Spain.
C DíazDepartment of Medical Sciences, School of Medicine, University of Castilla-La Mancha, Albacete, E02006, Spain.
J L FerranDepartment of Human Anatomy and Psychobiology, School of Medicine, University of Murcia, Murcia, E30071, Spain.
Universidad de Murcia · ESUniversity of Castilla-La Mancha · ESCincinnati Children's Hospital Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The telencephalic subpallium is the source of various GABAergic interneuron cohorts that invade the pallium via tangential migration. Based on genoarchitectonic studies, the subpallium has been subdivided into four major domains: striatum, pallidum, diagonal area and preoptic area (Puelles et al. 2013; Allen Developing Mouse Brain Atlas), and a larger set of molecularly distinct progenitor areas (Flames et al. 2007). Fate mapping, genetic lineage-tracing studies, and other approaches have suggested that each subpallial subdivision produces specific sorts of inhibitory interneurons, distinguished by differential peptidic content, which are distributed tangentially to pallial and subpallial target territories (e.g., olfactory bulb, isocortex, hippocampus, pallial and subpallial amygdala, striatum, pallidum, septum). In this report, we map descriptively the early differentiation and apparent migratory dispersion of mouse subpallial somatostatin-expressing (Sst) cells from E10.5 onward, comparing their topography with the expression patterns of the genes Dlx5, Gbx2, Lhx7-8, Nkx2.1, Nkx5.1 (Hmx3), and Shh, which variously label parts of the subpallium. Whereas some experimental results suggest that Sst cells are pallidal, our data reveal that many, if not most, telencephalic Sst cells derive from de diagonal area (Dg). Sst-positive cells initially only present at the embryonic Dg selectively populate radially the medial part of the bed nucleus striae terminalis (from paraseptal to amygdaloid regions) and part of the central amygdala; they also invade tangentially the striatum, while eschewing the globus pallidum and the preoptic area, and integrate within most cortical and nuclear pallial areas between E10.5 and E16.5.

Indexed as

Cell MovementAnimalsCell DifferentiationMiceNeural PathwaysNeuronsRNA, MessengerSomatostatinTelencephalonRNA, MessengerSomatostatinCortexEntopeduncular areaForebrain interneuronsMedial ganglionic eminencePallidumPreoptic areaSecondary prosencephalonStriatumSubpallium

Identifiers

PMID26189100
PMCPMC4920861
OpenAlexW1629081823

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.