Evidence map›Paper›PMID 35319900›Full record

ReviewAmerican journal of physiology. Cell physiology2022

Coreceptor functions of cell surface heparan sulfate proteoglycans.

Kazutaka Hayashida, Rafael S Aquino, Pyong Woo Park

Open access · greenAbstract readReview
In one paragraph

Review in American journal of physiology. Cell physiology, 2022. 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
5.5field-weighted citation impact, top 3% 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, 49 citations in OpenAlex.

  1. Effects of DietaryAnimals : an open access journal from MDPI · 2026
    Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Heparan Sulfate Proteoglycans in Immunity.Proteoglycan research · 2026
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Epithelial Heparan Sulfate PromotesProteoglycan research · 2025
    Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. 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

3 authors at 1 institution in 1 country.

Kazutaka HayashidaDepartment of Medicine, Boston Children's Hospital, Boston, Massachusetts.
Rafael S AquinoDepartment of Medicine, Boston Children's Hospital, Boston, Massachusetts.
Pyong Woo ParkDepartment of Medicine, Boston Children's Hospital, Boston, Massachusetts.ORCID 0000-0002-7979-4979
Boston Children's Hospital · US

Funding

Syndecan Regulation of Sepsis Host DefenseR01HL142213 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI PARK, PYONG WOO · 2018 to 2021
$2.0M
Proteoglycan-Chemokine Interactions in Lung DiseaseR01HL132573 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI PARK, PYONG WOO · 2017 to 2020
$1.9M
Subversion of Syndecan-1 Functions in ListeriosisR21AI156284 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI PARK, PYONG WOO · 2021 to 2022
$487k
HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01HL132573HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01HL142213HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) R21AI156284NHLBI NIH HHS R01 HL132573NHLBI NIH HHS R01 HL142213NIAID NIH HHS R21 AI156284
6 · The paper itself

Abstract

Receptor-ligand interactions play an important role in many biological processes by triggering specific cellular responses. These interactions are frequently regulated by coreceptors that facilitate, alter, or inhibit signaling. Coreceptors work in parallel with other specific and accessory molecules to coordinate receptor-ligand interactions. Cell surface heparan sulfate proteoglycans (HSPGs) function as unique coreceptors because they can bind to many ligands and receptors through their HS and core protein motifs. Cell surface HSPGs are typically expressed in abundance of the signaling receptors and, thus, are capable of mediating the initial binding of ligands to the cell surface. HSPG coreceptors do not possess kinase domains or intrinsic enzyme activities and, for the most part, binding to cell surface HSPGs does not directly stimulate intracellular signaling. Because of these features, cell surface HSPGs primarily function as coreceptors for many receptor-ligand interactions. Given that cell surface HSPGs are widely conserved, they likely serve fundamental functions to preserve basic physiological processes. Indeed, cell surface HSPGs can support specific cellular interactions with growth factors, morphogens, chemokines, extracellular matrix (ECM) components, and microbial pathogens and their secreted virulence factors. Through these interactions, HSPG coreceptors regulate cell adhesion, proliferation, migration, and differentiation, and impact the onset, progression, and outcome of pathophysiological processes, such as development, tissue repair, inflammation, infection, and tumorigenesis. This review seeks to provide an overview of the various mechanisms of how cell surface HSPGs function as coreceptors.

Indexed as

Heparan Sulfate ProteoglycansSignal TransductionCell MembraneHeparan SulfateIntercellular Signaling Peptides and ProteinsLigandsHeparan SulfateHeparan Sulfate ProteoglycansIntercellular Signaling Peptides and ProteinsLigandscoreceptorheparan sulfateproteoglycanreceptor-ligand interactionsignaling

Identifiers

PMID35319900
PMCPMC9109798
OpenAlexW4221090085

What Socratic 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 Socratic graph.