Evidence map›Paper›PMID 9364056›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience1997

Phosphodiesterase I, a novel adhesion molecule and/or cytokine involved in oligodendrocyte function.

B Fuss, H Baba, T Phan, V K Tuohy, W B Macklin

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

37 citing papers in PubMed, 103 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. International journal of molecular sciences · 2021
    Article
  6. Reduced Serum and Cerebrospinal Fluid Levels of Autotaxin in Major Depressive Disorder.The international journal of neuropsychopharmacology · 2019
    Article
  7. Review
  8. Article
  9. Observational
  10. Review
  11. The Autotaxin-Lysophosphatidic Acid Axis Modulates Histone Acetylation and Gene Expression during Oligodendrocyte Differentiation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  12. Autotaxin: structure-function and signaling.Journal of lipid research · 2014
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Aiming drug discovery at lysophosphatidic acid targets.British journal of pharmacology · 2010
    Review
  20. Autotaxin.Cellular and molecular life sciences : CMLS · 2009
    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

5 authors at 2 institutions in 2 countries.

B FussDepartment of Neurosciences, Research Institute, The Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.
H Baba
T Phan
V K Tuohy
W B Macklin
Cleveland Foundation · USNational Institute for Physiological Sciences · JP

Funding

MYFLIN PROTEIN GENE EXPRESSIONR01NS025304 · NINDS · UNIVERSITY OF COLORADO DENVER · PI MACKLIN, WENDY B · 1987 to 2013
$3.3M
NINDS NIH HHS R01 NS025304
6 · The paper itself

Abstract

One of the more complex developmental processes occurring postnatally in the CNS is the formation of the myelin sheath by oligodendrocytes. To examine the molecular events that take place during myelination, we isolated oligodendrocyte-derived cDNA clones, one of which (p421.HB) represents a putative alternatively spliced isoform of rat brain-specific phosphodiesterase I (PD-Ialpha) and a species homolog of the human cytokine autotaxin. Analysis of the structural composition of the p421.HB/PD-Ialpha protein suggests a transmembrane-bound ectoenzyme, which, in addition to the phosphodiesterase-active site contains presumed cell recognition and Ca2+-binding domains. Consequently, it may be involved in extracellular signaling events. Expression of p421.HB/PD-Ialpha is enriched in brain and spinal cord, where its mRNA can be detected in oligodendrocytes and in cells of the choroid plexus. Expression in the brain increases during development with an intermediate peak of expression around the time of active myelination and maximal expression in the adult. We have identified four presumably alternatively spliced isoforms, two of which appear to be CNS-specific. Decreased levels of p421.HB/PD-Ialpha mRNA in the dysmyelinating mouse mutant jimpy, but not shiverer, suggest a role for p421.HB/PD-Ialpha during active myelination and/or late stages of oligodendrocyte differentiation. Furthermore, p421.HB/PD-Ialpha mRNA levels were reduced in the CNS at onset of clinical symptoms in experimental autoimmune encephalomyelitis. These data together implicate the importance of p421.HB/PD-Ialpha in oligodendrocyte function, possibly through cell-cell and/or cell-extracellular matrix recognition.

Indexed as

AnimalsAutoimmune DiseasesCell AdhesionCell DifferentiationCentral Nervous SystemChoroid PlexusDNA, ComplementaryEncephalomyelitis, Autoimmune, ExperimentalEnzyme InductionExtracellular MatrixFemaleGene Expression Regulation, DevelopmentalIsoenzymesMaleMiceMice, JimpyDNA, ComplementaryIsoenzymesNerve Tissue ProteinsPhosphodiesterase IPhosphoric Diester HydrolasesRNA, Messenger

Identifiers

PMID9364056
PMCPMC6573621
OpenAlexW2170335529

What OpenQuestion holds

Textmetadata
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.