Evidence map›Paper›PMID 27110779›Full record

ArticleInternational journal of molecular sciences2016

Epigenetic Modulation of Human Induced Pluripotent Stem Cell Differentiation to Oligodendrocytes.

Panagiotis Douvaras, Tomasz Rusielewicz, Kwi Hye Kim, Jeffery D Haines, Patrizia Casaccia, Valentina Fossati

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. The epigenetic landscape of oligodendrocyte lineage cells.Annals of the New York Academy of Sciences · 2023
    Review
  6. Review
  7. Epigenetic Regulation of Optic Nerve Development, Protection, and Repair.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Therapeutic Plasticity of Neural Stem Cells.Frontiers in neurology · 2020
    Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. 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

6 authors at 2 institutions in 1 country.

Panagiotis DouvarasThe New York Stem Cell Foundation Research Institute, New York, NY 10032, USA. pdouvaras@nyscf.org.
Tomasz RusielewiczThe New York Stem Cell Foundation Research Institute, New York, NY 10032, USA. trusielewicz@nyscf.org.
Kwi Hye KimDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA. kwihyekim@gmail.com.
Jeffery D HainesDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA. jefferyhaines@gmail.com.
Patrizia CasacciaDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA. patrizia.casaccia@mssm.edu.
Valentina FossatiThe New York Stem Cell Foundation Research Institute, New York, NY 10032, USA. vfossati@nyscf.org.
Icahn School of Medicine at Mount Sinai · USNew York Stem Cell Foundation · US

Funding

Histone Deacetylation in Oligodendrocyte DifferentiationR37NS042925 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CASACCIA, PATRIZIA · 2012 to 2018
$4.3M
NINDS NIH HHS R37 NS042925
6 · The paper itself

Abstract

Pluripotent stem cells provide an invaluable tool for generating human, disease-relevant cells. Multiple sclerosis is an inflammatory demyelinating disease of the central nervous system, characterized by myelin damage. Oligodendrocytes are the myelinating cells of the central nervous system (CNS); they differentiate from progenitor cells, and their membranes ensheath axons, providing trophic support and allowing fast conduction velocity. The current understanding of oligodendrocyte biology was founded by rodent studies, where the establishment of repressive epigenetic marks on histone proteins, followed by activation of myelin genes, leads to lineage progression. To assess whether this epigenetic regulation is conserved across species, we differentiated human embryonic and induced pluripotent stem cells to oligodendrocytes and asked whether similar histone marks and relative enzymatic activities could be detected. The transcriptional levels of enzymes responsible for methylation and acetylation of histone marks were analyzed during oligodendrocyte differentiation, and the post-translational modifications on histones were detected using immunofluorescence. These studies showed that also in human cells, differentiation along the oligodendrocyte lineage is characterized by the acquisition of multiple repressive histone marks, including deacetylation of lysine residues on histone H3 and trimethylation of residues K9 and K27. These data suggest that the epigenetic modulation of oligodendrocyte identity is highly conserved across species.

Indexed as

Epigenesis, GeneticAcetylationBasic Helix-Loop-Helix ProteinsCell DifferentiationCells, CulturedHistonesHumansInduced Pluripotent Stem CellsMicroscopy, FluorescenceNerve Tissue ProteinsOligodendrocyte Transcription Factor 2OligodendrogliaPAX6 Transcription FactorProtein Processing, Post-TranslationalBasic Helix-Loop-Helix ProteinsHistonesNerve Tissue ProteinsOLIG2 protein, humanOligodendrocyte Transcription Factor 2PAX6 Transcription Factorhistone modificationshuman induced pluripotent stem cellsoligodendrocyte differentiation

Identifiers

PMID27110779
PMCPMC4849063
OpenAlexW2337692346

What OpenQuestion holds

Textmetadata
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.