Evidence map›Paper›PMID 24848099›Full record

ArticlePloS one2014

Comparison of the gene expression profiles of human fetal cortical astrocytes with pluripotent stem cell derived neural stem cells identifies human astrocyte markers and signaling pathways and transcription factors active in human astrocytes.

Nasir Malik, Xiantao Wang, Sonia Shah, Anastasia G Efthymiou, Bin Yan, Sabrina Heman-Ackah, Ming Zhan, Mahendra Rao

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

28 citing papers in PubMed, 46 citations in OpenAlex.

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  8. Mature iPSC-derived astrocytes of an ALS/FTD patient carrying the TDP43Frontiers in cell and developmental biology · 2023
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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

8 authors at 5 institutions in 2 countries.

Nasir MalikNational Institutes of Health, NIAMS, Bethesda, Maryland, United States of America.
Xiantao WangNational Institutes of Health, NIAMS, Bethesda, Maryland, United States of America.
Sonia ShahNational Institutes of Health, NIAMS, Bethesda, Maryland, United States of America.
Anastasia G EfthymiouNational Institutes of Health, NIAMS, Bethesda, Maryland, United States of America.
Bin YanHong Kong Baptist University, Department of Biology, Hong Kong.
Sabrina Heman-AckahNational Institutes of Health, NIAMS, Bethesda, Maryland, United States of America.
Ming ZhanThe Methodist Hospital Research Institute, Weill Cornell Medical College, Houston, Texas, United States of America.
Mahendra RaoNational Institutes of Health, NIAMS, Bethesda, Maryland, United States of America; National Institutes of Health, NIH Center for Regenerative Medicine, Bethesda, Maryland, United States of America.
National Institutes of Health · USCenter for Neuroscience and Regenerative Medicine · USCornell University · USHong Kong Baptist University · HKNational Institute of Arthritis and Musculoskeletal and Skin Diseases · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Astrocytes are the most abundant cell type in the central nervous system (CNS) and have a multitude of functions that include maintenance of CNS homeostasis, trophic support of neurons, detoxification, and immune surveillance. It has only recently been appreciated that astrocyte dysfunction is a primary cause of many neurological disorders. Despite their importance in disease very little is known about global gene expression for human astrocytes. We have performed a microarray expression analysis of human fetal astrocytes to identify genes and signaling pathways that are important for astrocyte development and maintenance. Our analysis confirmed that the fetal astrocytes express high levels of the core astrocyte marker GFAP and the transcription factors from the NFI family which have been shown to play important roles in astrocyte development. A group of novel markers were identified that distinguish fetal astrocytes from pluripotent stem cell-derived neural stem cells (NSCs) and NSC-derived neurons. As in murine astrocytes, the Notch signaling pathway appears to be particularly important for cell fate decisions between the astrocyte and neuronal lineages in human astrocytes. These findings unveil the repertoire of genes expressed in human astrocytes and serve as a basis for further studies to better understand astrocyte biology, especially as it relates to disease.

Indexed as

TranscriptomeAstrocytesBiomarkersCell DedifferentiationCells, CulturedCerebral CortexFetusGene OntologyHumansInduced Pluripotent Stem CellsNeural Stem CellsOligonucleotide Array Sequence AnalysisSignal TransductionTranscription FactorsUp-RegulationBiomarkersTranscription Factors

Identifiers

PMID24848099
PMCPMC4029581
OpenAlexW2058834995

What OpenQuestion holds

Textmetadata
LicenceCC0
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.