Evidence map›Paper›PMID 31484369›Full record

ArticleCells2019

Potential of Adult Endogenous Neural Stem/Progenitor Cells in the Spinal Cord to Contribute to Remyelination in Experimental Autoimmune Encephalomyelitis.

Yuki Maeda, Nami Nakagomi, Akiko Nakano-Doi, Hiroto Ishikawa, Yoshiki Tatsumi, Yoshio Bando, Hiroo Yoshikawa, Tomohiro Matsuyama, Fumi Gomi, Takayuki Nakagomi

Open access · goldAbstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Distribution, contribution and regulation of nestinJournal of advanced research · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Neurogenesis as a Tool for Spinal Cord Injury.International journal of molecular sciences · 2022
    Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Aging, Cellular Senescence, and Progressive Multiple Sclerosis.Frontiers in cellular neuroscience · 2020
    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

10 authors at 2 institutions in 1 country.

Yuki MaedaDepartment of Ophthalmology, Hyogo College of Medicine, 1-1 Mukogawacho, Nishinomiya, Hyogo 663-8501, Japan. ds28043@hyo-med.ac.jp.
Nami NakagomiDepartment of Surgical Pathology, Hyogo College of Medicine, 1-1 Mukogawacho, Nishinomiya, Hyogo 663-8501, Japan. na-nakagomi@hyo-med.ac.jp.
Akiko Nakano-DoiInstitute for Advanced Medical Sciences, Hyogo College of Medicine, 1-1 Mukogawacho, Nishinomiya, Hyogo 663-8501, Japan. nakano@hyo-med.ac.jp.
Hiroto IshikawaDepartment of Ophthalmology, Hyogo College of Medicine, 1-1 Mukogawacho, Nishinomiya, Hyogo 663-8501, Japan. ohmyeye@gmail.com.ORCID 0000-0003-0760-7203
Yoshiki TatsumiDivision of Neurology, Department of Internal Medicine, Hyogo College of Medicine, 1-1 Mukogawacho, Nishinomiya, Hyogo 663-8501, Japan. ytatsumi@hyo-med.ac.jp.
Yoshio BandoDepartment of Anatomy, Akita University Graduate School of Medicine, 1-1-1 Hondo, Akita, Akita 010-8543, Japan. ybando@med.akita-u.ac.jp.
Hiroo YoshikawaDivision of Neurology, Department of Internal Medicine, Hyogo College of Medicine, 1-1 Mukogawacho, Nishinomiya, Hyogo 663-8501, Japan. hyoshika@hyo-med.ac.jp.
Tomohiro MatsuyamaDepartment of Therapeutic Progress in Brain Diseases, Hyogo College of Medicine, 1-1 Mukogawacho, Nishinomiya, Hyogo 663-8501, Japan. tomohiro@hyo-med.ac.jp.
Fumi GomiDepartment of Ophthalmology, Hyogo College of Medicine, 1-1 Mukogawacho, Nishinomiya, Hyogo 663-8501, Japan. fgomi@hyo-med.ac.jp.
Takayuki NakagomiInstitute for Advanced Medical Sciences, Hyogo College of Medicine, 1-1 Mukogawacho, Nishinomiya, Hyogo 663-8501, Japan. nakagomi@hyo-med.ac.jp.ORCID 0000-0003-2274-410X
Hyogo Medical University · JPAkita University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Demyelination and remyelination play pivotal roles in the pathological process of multiple sclerosis (MS) and experimental autoimmune encephalomyelitis (EAE), a well-established animal model of MS. Although increasing evidence shows that various stimuli can promote the activation/induction of endogenous neural stem/progenitor cells (NSPCs) in the central nervous system, the potential contributions of these cells to remyelination following inflammatory injury remain to be fully investigated. In the present study, using an adult mouse model of EAE induced by myelin oligodendrocyte glycoprotein (MOG) peptide, we investigated whether adult NSPCs in the spinal cord can lead to remyelination under inflammatory conditions. Immunohistochemistry showed that cells expressing the NSPC marker Nestin appeared after MOG peptide administration, predominantly at the sites of demyelination where abundant inflammatory cells had accumulated, whereas Nestin

Indexed as

NeurogenesisAnimalsAstrocytesCell LineageCells, CulturedEncephalomyelitis, Autoimmune, ExperimentalFemaleMiceMice, Inbred C57BLMyelin SheathNestinNeural Stem CellsOligodendrogliaSpinal CordNestinexperimental autoimmune encephalomyelitismultiple sclerosisNestinneural stem/progenitor cellsremyelinationspinal cord

Identifiers

PMID31484369
PMCPMC6769975
OpenAlexW2972251075

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.