Evidence map›Paper›PMID 1438217›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1992

Induction of the neural cell adhesion molecule and neuronal aggregation by osteogenic protein 1.

G Perides, R M Safran, D C Rueger, M E Charness

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
8.7field-weighted citation impact, top 2% 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

9 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Antagonists of alcohol inhibition of cell adhesion.Proceedings of the National Academy of Sciences of the United States of America · 2000
    Article
  3. Article
  4. Article
  5. Article
  6. The neural cell adhesion molecule (N-CAM) inhibits proliferation in primary cultures of rat astrocytes.Proceedings of the National Academy of Sciences of the United States of America · 1995
    Article
  7. Article
  8. Review
  9. Drosophila transforming growth factor beta superfamily proteins induce endochondral bone formation in mammals.Proceedings of the National Academy of Sciences of the United States of America · 1993
    Article
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

4 authors at 1 institution in 1 country.

G PeridesDepartment of Pathology, Harvard Medical School, West Roxbury, MA.
R M Safran
D C Rueger
M E Charness
Roxbury Community College · US

Funding

ETHANOL MODULATES OPIOID RECEPTORS IN NEURAL CELL LINESR01AA006662 · NIAAA · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI CHARNESS, MICHAEL EDWARD · 1985 to 1993
–
BRAIN SPECIFIC PROTEIN--GFA PROTEIN IN ASTROCYTESR01NS013034 · NINDS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI BIGNAMI, AMICO · 1985 to 1993
–
NIAAA NIH HHS AA06662NINDS NIH HHS NS13034
6 · The paper itself

Abstract

The neural cell adhesion molecule (N-CAM) plays a fundamental role in nervous system development and regeneration, yet the regulation of the expression of N-CAM in different brain regions has remained poorly understood. Osteogenic protein 1 (OP-1) is a member of the transforming growth factor beta superfamily that is expressed in the nervous system. Treatment of the neuroblastoma-glioma hybrid cell line NG108-15 for 1-4 days with recombinant human OP-1 (hOP-1) induced alterations in cell shape, formation of epithelioid sheets, and aggregation of cells into multilayered clusters. Immunofluorescence studies and Western blots demonstrated a striking differential induction of the three N-CAM isoforms in hOP-1-treated cells. hOP-1 caused a 6-fold up-regulation of the 140-kDa N-CAM, the isoform showing the highest constitutive expression, and a 29-fold up-regulation of the 180-kDa isoform. The 120-kDa isoform was not detected in control NG108-15 cells but was readily identified in hOP-1-treated cells. Incubation of NG108-15 cells with an antisense N-CAM oligonucleotide reduced the induction of N-CAM by hOP-1 and decreased the formation of multilayered cell aggregates. Anti-N-CAM monoclonal antibodies also diminished the formation of multilayered cell aggregates by hOP-1 and decreased cell-cell adhesion when hOP-1-treated NG108-15 cells were dispersed and replated. Thus, hOP-1 produces morphologic changes in NG108-15 cells, at least in part, by inducing N-CAM. These observations suggest that OP-1 or a homologue may participate in the regulation of N-CAM during nervous system development and regeneration.

Indexed as

Bone Morphogenetic ProteinsTransforming Growth Factor betaAnimalsAntibodies, MonoclonalBlotting, WesternBone Morphogenetic Protein 7Cell AdhesionCell Adhesion Molecules, NeuronalCell AggregationDose-Response Relationship, DrugFluorescent Antibody TechniqueGliomaKineticsMolecular WeightNeuroblastomaProteinsAntibodies, MonoclonalBMP7 protein, humanBone Morphogenetic Protein 7Bone Morphogenetic ProteinsCell Adhesion Molecules, NeuronalProteinsRecombinant ProteinsTransforming Growth Factor beta

Identifiers

PMID1438217
PMCPMC50331
OpenAlexW2062327119

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.