Evidence map›Paper›PMID 25745432›Full record

ArticleNeural regeneration research2012

Dorsal root ganglion progenitors differentiate to gamma-aminobutyric acid- and choline acetyltransferase-positive neurons.

Lingli Yu, Yindi Ding, Ambre Spencer, Ji Ma, Ruisheng Lu, Brian B Rudkin, Chonggang Yuan

Abstract read
In one paragraph

Article in Neural regeneration research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 52% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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 1 institution in 1 country.

Lingli YuLaboratory of Molecular and Cellular Neurophysiology, School of Life Science, East China Normal University, Shanghai 200062, China ; Differentiation & Cell Cycle Group, Laboratory of Molecular and Cellular Science, UMR 5239 CNRS/ENS Lyon/University of Lyon 1, Ecole Normale Supérieure de Lyon, IFR128 "Biosciences Lyon-Gerland" Lyon, 69007, France.
Yindi DingLaboratory of Molecular and Cellular Neurophysiology, School of Life Science, East China Normal University, Shanghai 200062, China ; Differentiation & Cell Cycle Group, Laboratory of Molecular and Cellular Science, UMR 5239 CNRS/ENS Lyon/University of Lyon 1, Ecole Normale Supérieure de Lyon, IFR128 "Biosciences Lyon-Gerland" Lyon, 69007, France.
Ambre SpencerLaboratory of Molecular and Cellular Neurophysiology, School of Life Science, East China Normal University, Shanghai 200062, China ; Differentiation & Cell Cycle Group, Laboratory of Molecular and Cellular Science, UMR 5239 CNRS/ENS Lyon/University of Lyon 1, Ecole Normale Supérieure de Lyon, IFR128 "Biosciences Lyon-Gerland" Lyon, 69007, France.
Ji MaLaboratory of Molecular and Cellular Neurophysiology, School of Life Science, East China Normal University, Shanghai 200062, China.
Ruisheng LuLaboratory of Molecular and Cellular Neurophysiology, School of Life Science, East China Normal University, Shanghai 200062, China.
Brian B RudkinLaboratory of Molecular and Cellular Neurophysiology, School of Life Science, East China Normal University, Shanghai 200062, China ; Differentiation & Cell Cycle Group, Laboratory of Molecular and Cellular Science, UMR 5239 CNRS/ENS Lyon/University of Lyon 1, Ecole Normale Supérieure de Lyon, IFR128 "Biosciences Lyon-Gerland" Lyon, 69007, France.
Chonggang YuanLaboratory of Molecular and Cellular Neurophysiology, School of Life Science, East China Normal University, Shanghai 200062, China.
East China Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study examined the isolation and differentiation of dorsal root ganglion progenitor cells for therapeutic use in neurodegenerative diseases. Rat embryonic dorsal root ganglia progenitors were isolated and purified using the differential adhesion method combined with cytosine arabinoside treatment. After culture in serum-free medium supplemented with B27, basic fibroblast growth factor and epidermal growth factor, these cells remained viable and survived for more than 18 months in vitro. Most cells differentiated to neurons that were immunoreactive for gamma-aminobutyric acid and choline acetyltransferase as detected by immunohistochemical staining. In addition, nerve growth factor and neurotrophic tyrosine kinase receptor expression were also observed in dorsal root ganglion progenitors and differentiated cells. K252a, an inhibitor that blocks nerve growth factor-induced signaling, inhibited cell survival, suggesting the possible existence of a nerve growth factor autocrine loop in these proliferating cells.

Indexed as

differentiation characterizationdorsal root ganglionnerve growth factorneural progenitortyrosine kinase receptor type 1

Identifiers

PMID25745432
PMCPMC4348992
OpenAlexW84945568

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.