Evidence map›Paper›PMID 23867465›Full record

ArticleThe Journal of biological chemistry2013

Heparan sulfate proteoglycans containing a glypican 5 core and 2-O-sulfo-iduronic acid function as Sonic Hedgehog co-receptors to promote proliferation.

Rochelle M Witt, Marie-Lyn Hecht, Maria F Pazyra-Murphy, Samuel M Cohen, Christian Noti, Toin H van Kuppevelt, Maria Fuller, Jennifer A Chan, John J Hopwood, Peter H Seeberger and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

36 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. Synthetic biology for heparin biomanufacturing.Bioresources and bioprocessing · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Coreceptor functions of cell surface heparan sulfate proteoglycans.American journal of physiology. Cell physiology · 2022
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Deciphering functional glycosaminoglycan motifs in development.Current opinion in structural biology · 2018
    Review
  20. The ADAMTS5 Metzincin Regulates Zebrafish Somite Differentiation.International journal of molecular sciences · 2018
    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

11 authors at 7 institutions in 6 countries.

Rochelle M WittFrom the Dana Farber Cancer Institute, Boston, Massachusetts 02215,; the Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02215.
Marie-Lyn Hechtthe Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1,14476 Potsdam, Germany,; the Federal Institute of Technology (ETH) Zürich, Wolfgang-Pauli-Str.10, CH-8093 Zürich, Switzerland.
Maria F Pazyra-MurphyFrom the Dana Farber Cancer Institute, Boston, Massachusetts 02215,; the Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02215.
Samuel M CohenFrom the Dana Farber Cancer Institute, Boston, Massachusetts 02215,; the Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02215.
Christian Notithe Federal Institute of Technology (ETH) Zürich, Wolfgang-Pauli-Str.10, CH-8093 Zürich, Switzerland.
Toin H van Kuppeveltthe Department of Biochemistry, Nijmegen Centre for Molecular Life Sciences, Radboud University, Nijmegen Medical Centre, P. O. Box 9101, 6500 HB Nijmegen, The Netherlands.
Maria Fullerthe Lysosomal Diseases Research Unit, SA Pathology at Women's and Children's Hospital, 72 King William Road, North Adelaide, South Australia 5006, Australia.
Jennifer A Chanthe Department of Pathology and Laboratory Medicine, University of Calgary, Calgary, Alberta T2N 4N1, Canada, and.
John J Hopwoodthe Lysosomal Diseases Research Unit, SA Pathology at Women's and Children's Hospital, 72 King William Road, North Adelaide, South Australia 5006, Australia.
Peter H Seebergerthe Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1,14476 Potsdam, Germany,; the Institute of Chemistry and Biochemistry, Freie Universität Berlin, Arnimallee 22, 14195 Berlin, Germany. Electronic address: peter.seeberger@mpikg.mpg.de.
Rosalind A SegalFrom the Dana Farber Cancer Institute, Boston, Massachusetts 02215,; the Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02215,. Electronic address: Rosalind_segal@dfci.harvard.edu.
Dana-Farber Cancer Institute · USETH Zurich · CHHarvard University · USSouth Australia Pathology · AUFreie Universität Berlin · DERadboud University Nijmegen · NLUniversity of Calgary · CA

Funding

Medical Scientist Training ProgramT32GM007753 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WALENSKY, LOREN DAVID · 1985 to 2021
$50.0M
Training in the Molecular Biology of Neurodegeneration and Alzheimer's DiseaseT32AG000222 · NIA · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI Bruce A YANKNER · 1992 to 2026
$18.5M
NIH Director's Pioneer AwardDP1OD000839 · OD · DANA-FARBER CANCER INST · PI SEGAL, ROSALIND A. · 2006 to 2010
$4.3M
NCCDPHP CDC HHS DP1 0D000839NIA NIH HHS T32 AG000222NIGMS NIH HHS T32 GM007753
6 · The paper itself

Abstract

Sonic Hedgehog (Shh) signaling is crucial for growth, cell fate determination, and axonal guidance in the developing nervous system. Although the receptors Patched (Ptch1) and Smoothened (Smo) are required for Shh signaling, a number of distinct co-receptors contribute to these critical responses to Shh. Several membrane-embedded proteins such as Boc, Cdo, and Gas1 bind Shh and promote signaling. In addition, heparan sulfate proteoglycans (HSPGs) have also been implicated in the initiation of Shh responses. However, the attributes of HSPGs that function as co-receptors for Shh have not yet been defined. Here, we identify HSPGs containing a glypican 5 core protein and 2-O-sulfo-iduronic acid residues at the nonreducing ends of the glycans as co-receptors for Shh. These HSPG co-receptors are expressed by cerebellar granule cell precursors and promote Shh binding and signaling. At the subcellular level, these HSPG co-receptors are located adjacent to the primary cilia that act as Shh signaling organelles. Thus, Shh binds to HSPG co-receptors containing a glypican 5 core and 2-O-sulfo-iduronic acid to promote neural precursor proliferation.

Indexed as

Cell ProliferationAnimalsCerebellumChlorocebus aethiopsCOS CellsGene Expression RegulationGlypicansHedgehog ProteinsHEK293 CellsHumansMiceNerve Tissue ProteinsNeural Stem CellsSignal TransductionGlypicansGPC5 protein, humanGpc5 protein, mouseHedgehog ProteinsNerve Tissue ProteinsSHH protein, humanShh protein, mouseCerebellumHedgehogNeurodevelopmentProliferationProteoglycan

Identifiers

PMID23867465
PMCPMC3764831
OpenAlexW1998316337

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.