Evidence map›Paper›PMID 25169049›Full record

ReviewJournal of neuroscience methods2014

Finding degrees of separation: experimental approaches for astroglial and oligodendroglial cell isolation and genetic targeting.

Li-Jin Chew, Cynthia A DeBoy, Vladimir V Senatorov

Abstract readReview
In one paragraph

Review in Journal of neuroscience methods, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Review
  3. Frontiers in cell and developmental biology · 2020
    Review
  4. Article
  5. Review
  6. Review
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

3 authors.

Li-Jin ChewCenter for Neuroscience Research, Children's Research Institute, Children's National Medical Center, Washington, DC, United States. Electronic address: LChew@childrensnational.org.
Cynthia A DeBoyBiology Department, Trinity Washington University, Washington, DC, United States.
Vladimir V SenatorovHelen Wills Neuroscience Institute, University of California, Berkeley, CA, United States.

Funding

Characterization of Sox17 as a Regulator of Oligodendrocyte Cell DifferentiationR01NS056427 · NINDS · CHILDREN'S RESEARCH INSTITUTE · PI VITTORIO GALLO, VITTORIO GALLO VITTORIO GALLO · 2007 to 2011
$1.8M
Long term consequences of white matter damage by perinatal hyperoxia.R21NS078731 · NINDS · CHILDREN'S RESEARCH INSTITUTE · PI VITTORIO GALLO, VITTORIO GALLO VITTORIO GALLO · 2012 to 2013
$460k
NINDS NIH HHS R01 NS056427NINDS NIH HHS R01NS056427NINDS NIH HHS R21 NS078731NINDS NIH HHS R21NS078731
6 · The paper itself

Abstract

The study of CNS glial cell function requires experimental methods to detect, purify, and manipulate each cell population with fidelity and specificity. With the identification and cloning of cell- and stage-specific markers, glial cell analysis techniques have grown beyond physical methods of tissue dissociation and cell culture, and become highly specific with immunoselection of cell cultures in vitro and genetic targeting in vivo. The unique plasticity of glial cells offers the potential for cell replacement therapies in neurological disease that utilize neural cells derived from transplanted neural stem and progenitor cells. In this mini-review, we outline general physical and genetic approaches for macroglial cell generation. We summarize cell culture methods to obtain astrocytes and oligodendrocytes and their precursors, from developing and adult tissue, as well as approaches to obtain human neural progenitor cells through the establishment of stem cells. We discuss popular targeting rodent strains designed for cell-specific detection, selection and manipulation of neuroglial cell progenitors and their committed progeny. Based on shared markers between astrocytes and stem cells, we discuss genetically modified mouse strains with overlapping expression, and highlight SOX-expressing strains available for targeting of stem and progenitor cell populations. We also include recently established mouse strains for detection, and tag-assisted RNA and miRNA analysis. This discussion aims to provide a brief overview of the rapidly expanding collection of experimental approaches and genetic resources for the isolation and targeting of macroglial cells, their sources, progeny and gene products to facilitate our understanding of their properties and potential application in pathology.

Indexed as

AnimalsAstrocytesCell Culture TechniquesCell SeparationGene TargetingHumansModels, GeneticOligodendrogliaStem CellsAstrocytesCell purificationGenetic targetingNeural precursorOligodendrogliaTransgenic mice

Identifiers

PMID25169049
PMCPMC4171043

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.