Evidence map›Paper›PMID 33492553›Full record

ArticleBrain structure & function2021

Sim1-expressing cells illuminate the origin and course of migration of the nucleus of the lateral olfactory tract in the mouse amygdala.

Elena Garcia-Calero, Lara López-González, Margaret Martínez-de-la-Torre, Chen-Ming Fan, Luis Puelles

Open access · hybridAbstract read
In one paragraph

Article in Brain structure & function, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 24 citations in OpenAlex.

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  6. Synaptic Connectivity and Electrophysiological Properties of the Nucleus of the Lateral Olfactory Tract.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
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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

5 authors at 2 institutions in 2 countries.

Elena Garcia-CaleroUniversity of Murcia, IMIB-Arrixaca Institute of Biomedical Research, 30120, El Palmar, Murcia, Spain. ecalero@um.es.ORCID http://orcid.org/0000-0002-7184-9584
Lara López-GonzálezUniversity of Murcia, IMIB-Arrixaca Institute of Biomedical Research, 30120, El Palmar, Murcia, Spain.
Margaret Martínez-de-la-TorreUniversity of Murcia, IMIB-Arrixaca Institute of Biomedical Research, 30120, El Palmar, Murcia, Spain.
Chen-Ming FanDepartment of Embryology, Carnegie Institution for Science, 3520 San Martin Drive, Baltimore, MD, 21218, USA.
Luis PuellesUniversity of Murcia, IMIB-Arrixaca Institute of Biomedical Research, 30120, El Palmar, Murcia, Spain.ORCID http://orcid.org/0000-0002-9541-7073
Instituto Murciano de Investigación Biosanitaria · ESCarnegie Institution for Science · US

Funding

FUNCTION OF MAMMALIAN SINGLE MINDED GENES, SIM1 AND SIM2R01HD035596 · NICHD · CARNEGIE INSTITUTION OF WASHINGTON, D.C. · PI FAN, CHEN-MING · 1998 to 2009
$2.4M
NICHD NIH HHS R01 HD035596
6 · The paper itself

Abstract

We focus this report on the nucleus of the lateral olfactory tract (NLOT), a superficial amygdalar nucleus receiving olfactory input. Mixed with its Tbr1-expressing layer 2 pyramidal cell population (NLOT2), there are Sim1-expressing cells whose embryonic origin and mode of arrival remain unclear. We examined this population with Sim1-ISH and a Sim1-tauLacZ mouse line. An alar hypothalamic origin is apparent at the paraventricular area, which expresses Sim1 precociously. This progenitor area shows at E10.5 a Sim1-expressing dorsal prolongation that crosses the telencephalic stalk and follows the terminal sulcus, reaching the caudomedial end of the pallial amygdala. We conceive this Sim1-expressing hypothalamo-amygdalar corridor (HyA) as an evaginated part of the hypothalamic paraventricular area, which participates in the production of Sim1-expressing cells. From E13.5 onwards, Sim1-expressing cells migrated via the HyA penetrate the posterior pallial amygdalar radial unit and associate therein to the incipient Tbr1-expressing migration stream which swings medially past the amygdalar anterior basolateral nucleus (E15.5), crosses the pallio-subpallial boundary (E16.5), and forms the NLOT2 within the anterior amygdala by E17.5. We conclude that the Tbr1-expressing NLOT2 cells arise strictly within the posterior pallial amygdalar unit, involving a variety of required gene functions we discuss. Our results are consistent with the experimental data on NLOT2 origin reported by Remedios et al. (Nat Neurosci 10:1141-1150, 2007), but we disagree on their implication in this process of the dorsal pallium, observed to be distant from the amygdala.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsCell MovementCorticomedial Nuclear ComplexHypothalamusMiceNeuronsRepressor ProteinsBasic Helix-Loop-Helix ProteinsRepressor ProteinsSim1 protein, mouseHypothalamo-amygdalar corridorHypothalamusPallial amygdalaPallium modelsParaventricular nucleusSubpallial amygdala

Identifiers

PMID33492553
PMCPMC7910384
OpenAlexW3123417535

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Registered trials

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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.