Evidence map›Paper›PMID 33318418›Full record

ReviewNeural regeneration research2021

Dynamic glial response and crosstalk in demyelination-remyelination and neurodegeneration processes.

Tianci Chu, Lisa B E Shields, Wenxin Zeng, Yi Ping Zhang, Yuanyi Wang, Gregory N Barnes, Christopher B Shields, Jun Cai

Abstract readReview
In one paragraph

Review in Neural regeneration research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. The role of monocytes in optic nerve injury.Neural regeneration research · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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

8 authors.

Tianci ChuPediatric Research Institute, Department of Pediatrics, University of Louisville School of Medicine, Louisville, KY, USA.
Lisa B E ShieldsNorton Neuroscience Institute, Norton Healthcare, Louisville, KY, USA.
Wenxin ZengPediatric Research Institute, Department of Pediatrics, University of Louisville School of Medicine, Louisville, KY, USA.
Yi Ping ZhangNorton Neuroscience Institute, Norton Healthcare, Louisville, KY, USA.
Yuanyi WangDepartment of Spine Surgery, The First Hospital of Jilin University, Changchun, Jilin Province, China.
Gregory N BarnesPediatric Research Institute, Department of Pediatrics; Department of Neurology, University of Louisville School of Medicine; Department of Pharmacology and Toxicology, University of Louisville, Louisville, KY, USA.
Christopher B ShieldsNorton Neuroscience Institute, Norton Healthcare; Department of Neurological Surgery, University of Louisville School of Medicine, Louisville, KY, USA.
Jun CaiPediatric Research Institute, Department of Pediatrics, University of Louisville School of Medicine; Department of Pharmacology and Toxicology, University of Louisville, Louisville, KY, USA.

Funding

University of Louisville Center for Integrative Environmental Health SciencesP30ES030283 · NIEHS · UNIVERSITY OF LOUISVILLE · PI Amanda Jo LeBlanc · 2020 to 2026
$10.0M
HIF-1/p38 MAPK pathway in rotational acceleration-deceleration neonatal brain injuryR21NS098170 · NINDS · UNIVERSITY OF LOUISVILLE · PI CAI, JUN · 2018 to 2019
$424k
NIEHS NIH HHS P30 ES030283NINDS NIH HHS R21 NS098170
6 · The paper itself

Abstract

Multiple sclerosis is an autoimmune disease in which the immune system attacks the myelin sheath in the central nervous system. It is characterized by blood-brain barrier dysfunction throughout the course of multiple sclerosis, followed by the entry of immune cells and activation of local microglia and astrocytes. Glial cells (microglia, astrocytes, and oligodendrocyte lineage cells) are known as the important mediators of neuroinflammation, all of which play major roles in the pathogenesis of multiple sclerosis. Network communications between glial cells affect the activities of oligodendrocyte lineage cells and influence the demyelination-remyelination process. A finely balanced glial response may create a favorable lesion environment for efficient remyelination and neuroregeneration. This review focuses on glial response and neurodegeneration based on the findings from multiple sclerosis and major rodent demyelination models. In particular, glial interaction and molecular crosstalk are discussed to provide insights into the potential cell- and molecule-specific therapeutic targets to improve remyelination and neuroregeneration.

Indexed as

astrocytecrosstalkdemyelinationglial responsemicroglia/macrophagemultiple sclerosisneurodegenerationneuroinflammationoligodendrocyte lineage cellsremyelination

Identifiers

PMID33318418
PMCPMC8284258

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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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.