Evidence map›Paper›PMID 9362504›Full record

ArticleThe Journal of cell biology1997

Glypican and biglycan in the nuclei of neurons and glioma cells: presence of functional nuclear localization signals and dynamic changes in glypican during the cell cycle.

Y Liang, M Häring, P J Roughley, R K Margolis, R U Margolis

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

39 citing papers in PubMed, 127 citations in OpenAlex.

  1. Review
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  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Glycosylation alterations in lung and brain cancer.Advances in cancer research · 2015
    Review
  13. Heparan sulfate in the nucleus and its control of cellular functions.Matrix biology : journal of the International Society for Matrix Biology · 2014
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Antithetic roles of proteoglycans in cancer.Cellular and molecular life sciences : CMLS · 2012
    Review
  20. 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

5 authors at 3 institutions in 2 countries.

Y LiangDepartment of Pharmacology, New York University Medical Center, New York 10016, USA.
M Häring
P J Roughley
R K Margolis
R U Margolis
McGill University · CAColumbia University Irving Medical Center · USState University of New York · US

Funding

COMPLEX CARBOHYDRATES OF NERVOUS TISSUER01NS013876 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI MARGOLIS, RICHARD U · 1985 to 2001
$598k
STUDIES ON NERVOUS TISSUE GLYCOCONJUGATESR01NS009348 · NINDS · SUNY DOWNSTATE MEDICAL CENTER · PI MARGOLIS, RICHARD U · 1985 to 2000
$307k
NIMH NIH HHS MH-00129NINDS NIH HHS NS-09348NINDS NIH HHS NS-13876
6 · The paper itself

Abstract

We have investigated the expression patterns and subcellular localization in nervous tissue of glypican, a major glycosylphosphatidylinositol-anchored heparan sulfate proteoglycan that is predominantly synthesized by neurons, and of biglycan, a small, leucine-rich chondroitin sulfate proteoglycan. By laser scanning confocal microscopy of rat central nervous tissue and C6 glioma cells, we found that a significant portion of the glypican and biglycan immunoreactivity colocalized with nuclear staining by propidium iodide and was also seen in isolated nuclei. In certain regions, staining was selective, insofar as glypican and biglycan immunoreactivity in the nucleus was seen predominantly in a subpopulation of large spinal cord neurons. The amino acid sequences of both proteoglycans contain potential nuclear localization signals, and these were demonstrated to be functional based on their ability to target beta-galactosidase fusion proteins to the nuclei of transfected 293 cells. Nuclear localization of glypican beta-galactosidase or Fc fusion proteins in transfected 293 cells and C6 glioma cells was greatly reduced or abolished after mutation of the basic amino acids or deletion of the sequence containing the nuclear localization signal, and no nuclear staining was seen in the case of heparan sulfate and chondroitin sulfate proteoglycans that do not possess a nuclear localization signal, such as syndecan-3 or decorin (which is closely related in structure to biglycan). Transfection of COS-1 cells with an epitope-tagged glypican cDNA demonstrated transport of the full-length proteoglycan to the nucleus, and there are also dynamic changes in the pattern of glypican immunoreactivity in the nucleus of C6 cells both during cell division and correlated with different phases of the cell cycle. Our data therefore suggest that in certain cells and central nervous system regions, glypican and biglycan may be involved in the regulation of cell division and survival by directly participating in nuclear processes.

Indexed as

Cell CycleNuclear Localization SignalsAnimalsBiglycanCell LineCell NucleusExtracellular Matrix ProteinsFluorescent Antibody Technique, IndirectGliomaHeparan Sulfate ProteoglycansHumansMicroscopy, ConfocalNeuronsNuclear ProteinsProteoglycansRatsBGN protein, humanBgn protein, ratBiglycanExtracellular Matrix ProteinsHeparan Sulfate ProteoglycansNuclear Localization SignalsNuclear ProteinsProteoglycansRecombinant Proteins

Identifiers

PMID9362504
PMCPMC2139971
OpenAlexW1968496776

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LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

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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.