Evidence map›Paper›PMID 35411060›Full record

ArticleScientific reports2022

Heterogeneous fates of simultaneously-born neurons in the cortical ventricular zone.

Elia Magrinelli, Natalia Baumann, Robin Jan Wagener, Christelle Glangetas, Camilla Bellone, Denis Jabaudon, Esther Klingler

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. 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

7 authors at 2 institutions in 2 countries.

Elia MagrinelliDepartment of Basic Neurosciences, University of Geneva, 1211, Geneva, Switzerland.
Natalia BaumannDepartment of Basic Neurosciences, University of Geneva, 1211, Geneva, Switzerland.
Robin Jan WagenerDepartment of Basic Neurosciences, University of Geneva, 1211, Geneva, Switzerland.
Christelle GlangetasDepartment of Basic Neurosciences, University of Geneva, 1211, Geneva, Switzerland.
Camilla BelloneDepartment of Basic Neurosciences, University of Geneva, 1211, Geneva, Switzerland.
Denis JabaudonDepartment of Basic Neurosciences, University of Geneva, 1211, Geneva, Switzerland. denis.jabaudon@unige.ch.
Esther KlinglerDepartment of Basic Neurosciences, University of Geneva, 1211, Geneva, Switzerland. esther.klingler@unige.ch.
University of Geneva · CHUniversity Hospital Heidelberg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neocortical excitatory neurons belong to diverse cell types, which can be distinguished by their dates of birth, laminar location, connectivity, and molecular identities. During embryogenesis, apical progenitors (APs) located in the ventricular zone first give birth to deep-layer neurons, and next to superficial-layer neurons. While the overall sequential construction of neocortical layers is well-established, whether APs produce multiple neuron types at single time points of corticogenesis is unknown. To address this question, here we used FlashTag to fate-map simultaneously-born (i.e. isochronic) cohorts of AP daughter neurons at successive stages of corticogenesis. We reveal that early in corticogenesis, isochronic neurons differentiate into heterogeneous laminar, hodological and molecular cell types. Later on, instead, simultaneously-born neurons have more homogeneous fates. Using single-cell gene expression analyses, we identify an early postmitotic surge in the molecular heterogeneity of nascent neurons during which some early-born neurons initiate and partially execute late-born neuron transcriptional programs. Together, these findings suggest that as corticogenesis unfolds, mechanisms allowing increased homogeneity in neuronal output are progressively implemented, resulting in progressively more predictable neuronal identities.

Indexed as

NeurogenesisNeuronsCerebral CortexSingle-Cell Analysis

Identifiers

PMID35411060
PMCPMC9001674
OpenAlexW4223443999

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.