Evidence map›Paper›PMID 25946682›Full record

ArticleGlia2015

Apcdd1 stimulates oligodendrocyte differentiation after white matter injury.

Hyun Kyoung Lee, Dylan Laug, Wenyi Zhu, Jay M Patel, Kevin Ung, Benjamin R Arenkiel, Stephen P J Fancy, Carrie Mohila, Benjamin Deneen

Abstract read
In one paragraph

Article in Glia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Structure of WNT inhibitor adenomatosis polyposis coli down-regulated 1 (APCDD1), a cell-surface lipid-binding protein.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  5. Review
  6. Review
  7. Group I PAKs in myelin formation and repair of the central nervous system: what, when, and how.Biological reviews of the Cambridge Philosophical Society · 2022
    Review
  8. Article
  9. Article
  10. Article
  11. HIFα Regulates Developmental Myelination Independent of Autocrine Wnt Signaling.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Endothelial Wnt/β-catenin signaling reduces immune cell infiltration in multiple sclerosis.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  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

9 authors at 3 institutions in 1 country.

Hyun Kyoung LeeCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston, Texas.
Dylan LaugCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston, Texas.
Wenyi ZhuCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston, Texas.
Jay M PatelMedical Scientist Training Program, Baylor College of Medicine, Houston, Texas.
Kevin UngProgram in Developmental Biology, Baylor College of Medicine, Houston, Texas.
Benjamin R ArenkielProgram in Developmental Biology, Baylor College of Medicine, Houston, Texas.
Stephen P J FancyDepartment of Neurology, University of California, San Francisco, San Francisco, California.
Carrie MohilaDepartment of Pathology, Texas Children's Hospital, Houston, Texas.
Benjamin DeneenCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston, Texas.
Baylor College of Medicine · USTexas Children's Hospital · USUniversity of California, San Francisco · US

Funding

UNDERSTANDING FXTAS AMONG MALES WITH THE FMR1 PREMUTATIONP30HD024064 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI TOLIAS, KIMBERLY R · 1988 to 2013
$29.4M
Steps towards a paternal gene activation therapy for Angelman syndromeU54HD083092 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI NELSON, DAVID LOREN, SAMACO, RODNEY C · 2014 to 2019
$7.8M
Training In Cell and Gene TherapyT32HL092332 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI MALCOLM K. BRENNER, Bruno Di Stefano · 2008 to 2026
$6.9M
Transcriptional regulation of gliogenesis in the CNSR01NS071153 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI DENEEN, BENJAMIN · 2010 to 2022
$5.0M
MAPPING CONNECTIVITY ONTO POSTNATAL-BORN NEURONSR01NS078294 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI ARENKIEL, BENJAMIN R · 2012 to 2023
$3.6M
Training in Cell and Gene TherapyT32DK064717 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI HESLOP, HELEN E · 2003 to 2007
$880k
NHLBI NIH HHS 5-T32HL092332-08NHLBI NIH HHS T32 HL092332NICHD NIH HHS HD024064NICHD NIH HHS P30 HD024064NICHD NIH HHS U54 HD083092NIDDK NIH HHS T32 DK064717NINDS NIH HHS R01 NS071153NINDS NIH HHS R01 NS078294NINDS NIH HHS R01NS078294
6 · The paper itself

Abstract

Wnt signaling plays an essential role in developmental and regenerative myelination of the CNS, therefore it is critical to understand how the factors associated with the various regulatory layers of this complex pathway contribute to these processes. Recently, Apcdd1 was identified as a negative regulator of proximal Wnt signaling, however its role in oligodendrocyte (OL) differentiation and reymelination in the CNS remain undefined. Analysis of Apcdd1 expression revealed dynamic expression during OL development, where its expression is upregulated during differentiation. Functional studies using ex vivo and in vitro OL systems revealed that Apcdd1 promotes OL differentiation, suppresses Wnt signaling, and associates with β-catenin. Application of these findings to white matter injury (WMI) models revealed that Apcdd1 similarly promotes OL differentiation after gliotoxic injury in vivo and acute hypoxia ex vivo. Examination of Apcdd1 expression in white matter lesions from neonatal WMI and adult multiple sclerosis revealed its expression in subsets of oligodendrocyte (OL) precursors. These studies describe, for the first time, the role of Apcdd1 in OLs after WMI and reveal that negative regulators of the proximal Wnt pathway can influence regenerative myelination, suggesting a new therapeutic strategy for modulating Wnt signaling and stimulating repair after WMI.

Indexed as

Age FactorsAnimalsbeta CateninCell DifferentiationDisease Models, AnimalGene Expression Regulation, DevelopmentalGreen Fluorescent ProteinsHumansHypoxiaIntracellular Signaling Peptides and ProteinsIn Vitro TechniquesLysophosphatidylcholinesMembrane ProteinsMiceOligodendrogliaOrgan Culture TechniquesAPCDD1 protein, humanbeta CateninGreen Fluorescent ProteinsIntracellular Signaling Peptides and ProteinsLysophosphatidylcholinesMembrane ProteinsWnt ProteinsApcdd1oligodendrocytewhite matter injuryWnt signaling

Identifiers

PMID25946682
PMCPMC4534334
OpenAlexW2108777613

What OpenQuestion holds

Textmetadata
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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.