Evidence map›Paper›PMID 30872629›Full record

ArticleScientific reports2019

Differential potentials of neural progenitors for the generation of neurons and non-neuronal cells in the developing amniote brain.

Yuki Hashimoto, Hitoshi Gotoh, Katsuhiko Ono, Tadashi Nomura

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

4 authors.

Yuki HashimotoDevelopmental Neurobiology, Graduate School of Medicine, Kyoto Prefectural University of Medicine, 1-5 Shimogamo-hangi cho, Sakyoku, Kyoto, 606-0823, Japan.
Hitoshi GotohDevelopmental Neurobiology, Graduate School of Medicine, Kyoto Prefectural University of Medicine, 1-5 Shimogamo-hangi cho, Sakyoku, Kyoto, 606-0823, Japan.
Katsuhiko OnoDevelopmental Neurobiology, Graduate School of Medicine, Kyoto Prefectural University of Medicine, 1-5 Shimogamo-hangi cho, Sakyoku, Kyoto, 606-0823, Japan.
Tadashi NomuraDevelopmental Neurobiology, Graduate School of Medicine, Kyoto Prefectural University of Medicine, 1-5 Shimogamo-hangi cho, Sakyoku, Kyoto, 606-0823, Japan. tadnom@koto.kpu-m.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mature mammalian brains consist of variety of neuronal and non-neuronal cell types, which are progressively generated from embryonic neural progenitors through the embryonic and postnatal periods. However, it remains unknown whether all embryonic progenitors equivalently contribute to multiple cell types, or individual neural progenitors have variable potentials to generate specific cell types in a stochastic manner. Here, we performed population-level tracing of mouse embryonic neural progenitors by using Tol2-mediated genome integration vectors. We identified that neural progenitors in early embryonic stages predominantly contribute to cortical or subcortical neurons than astrocytes, ependymal cells, and neuroblasts in the postnatal brain. Notably, neurons and astrocytes were cumulatively labeled by the increase of total labeled cells, suggesting constant neurogenic and gliogenic potentials of individual neural progenitors. On the contrary, numbers of labeled ependymal cell are more fluctuated, implicating intrinsic variability of progenitor potentials for ependymal cell generation. Differential progenitor potentials that contribute to neurons, astrocytes, and ependymal cells were also detected in the developing avian pallium. Our data suggest evolutionary conservations of coherent and variable potentials of neural progenitors that generate multiple cell types in the developing amniote brain.

Indexed as

Cell DifferentiationAnimalsAstrocytesBrainCell LineageChick EmbryoChickensEpendymaFemaleGenetic VectorsMiceMice, Inbred ICRNeural Stem CellsNeurogenesisNeuronsPregnancyTransposases

Identifiers

PMID30872629
PMCPMC6418204

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.