Evidence map›Paper›PMID 28795331›Full record

ArticleMolecular neurobiology2018

Cells Expressing Prominin-1 in Neonatal Murine Inferior Colliculus Differentiate into Neurons and Glia.

Haruka Okazaki, Akira Kanda, Seiji Kanda, Takaki Shimono, Yasutaka Yun, Yoshiki Kobayashi, Zeyun Wang, Hisashi Ooka, Kensuke Suzuki, Dan Bui Van and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular neurobiology, 2018. 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
0.3field-weighted citation impact, top 44% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. A Subpopulation of Microglia Generated in the Adult Mouse Brain Originates from Prominin-1-Expressing Progenitors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  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

13 authors at 1 institution in 1 country.

Haruka OkazakiDepartment of Otolaryngology, Kansai Medical University|, Osaka, Japan.
Akira KandaDepartment of Otolaryngology, Kansai Medical University|, Osaka, Japan. akanda@hirakata.kmu.ac.jp.
Seiji KandaRegeneration Research Center for Intractable Diseases, Kansai Medical University, Osaka, Japan.
Takaki ShimonoRegeneration Research Center for Intractable Diseases, Kansai Medical University, Osaka, Japan.
Yasutaka YunDepartment of Otolaryngology, Kansai Medical University|, Osaka, Japan.
Yoshiki KobayashiDepartment of Otolaryngology, Kansai Medical University|, Osaka, Japan.
Zeyun WangRegeneration Research Center for Intractable Diseases, Kansai Medical University, Osaka, Japan.
Hisashi OokaDepartment of Otolaryngology, Kansai Medical University|, Osaka, Japan.
Kensuke SuzukiDepartment of Otolaryngology, Kansai Medical University|, Osaka, Japan.
Dan Bui VanDepartment of Otolaryngology, Kansai Medical University|, Osaka, Japan.
Koichi TomodaDepartment of Otolaryngology, Kansai Medical University|, Osaka, Japan.
Hiroshi IwaiDepartment of Otolaryngology, Kansai Medical University|, Osaka, Japan.
Toshimasa NishiyamaDepartment of Public Health, Kansai Medical University, Osaka, Japan.
Kansai Medical University · JP

Funding

Alumni Association of Kansai Medical University Katano GrantJapanese MEXT 18790740Kansai Medical University Research grant D2
6 · The paper itself

Abstract

Inferior colliculus (IC) is a major center for the integration and processing of acoustic information from ascending auditory pathways. Damage to the IC as well as normal aging can impair auditory function. Novel strategies such as stem cell (SC)-based regenerative therapy are required for functional recovery because mature neural cells have a minimal regenerative capacity after an injury. However, it is not known if there are neural stem cells (NSCs) in the IC. Herein, we screened for NSCs by surface marker analysis using flow cytometry. Isolated IC cells expressing prominin-1 (CD133) exhibited the cardinal NSC properties self-renewal capacity, expression of known NSC markers (SOX2 and nestin), and multipotency. Prominin-1-expressing cells from neonatal IC generated neurospheres, and culture of these neurospheres in differentiation-conditioned medium gave rise to gamma-aminobutyric acid-ergic (GABAergic) neurons, astrocytes, and oligodendrocytes. The presence of NSC-like cells in the IC has important implications for understanding IC development and for potential regenerative therapy.

Indexed as

AC133 AntigenAnimalsCell DifferentiationCells, Culturedgamma-Aminobutyric AcidInferior ColliculiMiceNeural Stem CellsNeurogenesisNeurogliaNeuronsAC133 Antigengamma-Aminobutyric AcidCentral auditory pathwayInferior colliculusNeural stem cellProminin-1

Identifiers

PMID28795331
PMCPMC5948249
OpenAlexW2742473924

What OpenQuestion holds

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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.