Evidence map›Paper›PMID 22889333›Full record

ArticleStem cells and development2012

A stable cranial neural crest cell line from mouse.

Mamoru Ishii, Athena C Arias, Liqiong Liu, Yi-Bu Chen, Marianne E Bronner, Robert E Maxson

Abstract read
In one paragraph

Article in Stem cells and development, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

77 citing papers in PubMed, 132 citations in OpenAlex.

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  13. Disruption of DNA methylation-mediated cranial neural crest proliferation and differentiation causes orofacial clefts in mice.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  17. Cranial Neural Crest Specific Deletion ofInternational journal of molecular sciences · 2023
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17 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

Mamoru IshiiDepartment of Biochemistry and Molecular Biology, USC/Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
Athena C Arias
Liqiong Liu
Yi-Bu Chen
Marianne E Bronner
Robert E Maxson
University of Southern California · USCalifornia Institute of Technology · US

Funding

TWIST AND Msx2 IN BOUNDARY FORMATION AND CRANIOSYNOSTOSISR01DE016320 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MAXSON, ROBERT E. · 2005 to 2014
$3.9M
Cellular and Molecular Mechanisms of Patterned Growth of the Mammalian SkullR01DE019650 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MAXSON, ROBERT E. · 2009 to 2013
$1.9M
CIHR TB1-01192NIDCR NIH HHS R01 DE016320NIDCR NIH HHS R01DE016320NIDCR NIH HHS R01 DE019650NIDCR NIH HHS R01DE019650
6 · The paper itself

Abstract

Cranial neural crest cells give rise to ectomesenchymal derivatives such as cranial bones, cartilage, smooth muscle, dentin, as well as melanocytes, corneal endothelial cells, and neurons and glial cells of the peripheral nervous system. Previous studies have suggested that although multipotent stem-like cells may exist during the course of cranial neural crest development, they are transient, undergoing lineage restriction early in embryonic development. We have developed culture conditions that allow cranial neural crest cells to be grown as multipotent stem-like cells. With these methods, we obtained 2 independent cell lines, O9-1 and i10-1, which were derived from mass cultures of Wnt1-Cre; R26R-GFP-expressing cells. These cell lines can be propagated and passaged indefinitely, and can differentiate into osteoblasts, chondrocytes, smooth muscle cells, and glial cells. Whole-genome expression profiling of O9-1 cells revealed that this line stably expresses stem cell markers (CD44, Sca-1, and Bmi1) and neural crest markers (AP-2α, Twist1, Sox9, Myc, Ets1, Dlx1, Dlx2, Crabp1, Epha2, and Itgb1). O9-1 cells are capable of contributing to cranial mesenchymal (osteoblast and smooth muscle) neural crest fates when injected into E13.5 mouse cranial tissue explants and chicken embryos. These results suggest that O9-1 cells represent multipotent mesenchymal cranial neural crest cells. The O9-1 cell line should serve as a useful tool for investigating the molecular properties of differentiating cranial neural crest cells.

Indexed as

Cell DifferentiationCell LineAnimalsBiomarkersCell Culture TechniquesCell MovementChick EmbryoCulture MediaFlow CytometryGene Expression ProfilingHyaluronan ReceptorsMiceMicroinjectionsMyocytes, Smooth MuscleNeural CrestNeurogliaBiomarkersCd44 protein, mouseCulture MediaHyaluronan Receptors

Identifiers

PMID22889333
PMCPMC3495126
OpenAlexW2170552323

What OpenQuestion holds

Textmetadata
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.