Evidence map›Paper›PMID 25892563›Full record

ReviewMatrix biology : journal of the International Society for Matrix Biology2015

Heparin interaction with a receptor on hyperglycemic dividing cells prevents intracellular hyaluronan synthesis and autophagy responses in models of type 1 diabetes.

Aimin Wang, Nehru Viji Sankaranarayanan, Masaki Yanagishita, Douglas M Templeton, Umesh R Desai, Kazuyuki Sugahara, Christina P Wang, Vincent C Hascall

Open access · hybridAbstract readReview
In one paragraph

Review in Matrix biology : journal of the International Society for Matrix Biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Introduction to the Molecules Special Edition Entitled 'Molecules (Basel, Switzerland) · 2019
    Article
  7. [Value of podocalyxin levels in urinary extracellular vesicles for diagnosis of diabetic nephropathy].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2018
    Article
  8. Review
  9. A current view of perlecan in physiology and pathology: A mosaic of functions.Matrix biology : journal of the International Society for Matrix Biology · 2017
    Review
  10. Endorepellin-evoked Autophagy Contributes to Angiostasis.The Journal of biological chemistry · 2016
    Article
  11. Article
  12. Article
  13. 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

8 authors at 5 institutions in 3 countries.

Aimin WangBiomedical Engineering, Cleveland Clinic, Cleveland, OH, United States.
Nehru Viji SankaranarayananDepartment of Medicinal Chemistry and Institute for Structural Biology, Virginia Commonwealth University, Richmond, VA, United States.
Masaki YanagishitaDivision of Biochemistry, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
Douglas M TempletonDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada.
Umesh R DesaiDepartment of Medicinal Chemistry and Institute for Structural Biology, Virginia Commonwealth University, Richmond, VA, United States.
Kazuyuki SugaharaDepartment of Pathobiochemistry, Faculty of Pharmacy, Meijo University, Nagoya, Japan.
Christina P WangBiomedical Engineering, Cleveland Clinic, Cleveland, OH, United States.
Vincent C HascallBiomedical Engineering, Cleveland Clinic, Cleveland, OH, United States. Electronic address: hascalv@ccf.org.
Cleveland Clinic · USVirginia Commonwealth University · USMeijo University · JPTokyo Medical and Dental University · JPUniversity of Toronto · CA

Funding

VERSICAN PROTEOLYSIS AND REGULATION OF VASCULAR SMOOTH MUSCLEP01HL107147 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI LAUER, MARK E · 2011 to 2017
$16.1M
Therapeutic assessment of synthetic heparin sulfates in transplantation modelsP01HL107152 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI DESAI, UMESH RAMANLAL · 2011 to 2017
$15.8M
NHLBI NIH HHS P01 HL 107147NHLBI NIH HHS P01 HL107147NHLBI NIH HHS P01 HL 107152NHLBI NIH HHS P01 HL107152
6 · The paper itself

Abstract

Previous studies and ongoing research indicate the importance of an interaction between a putative receptor on dividing cells in hyperglycemia and the non-reducing end motifs of heparin stored in mast cell secretory granules and how this interaction prevents activation of hyaluronan synthesis in intracellular compartments and subsequent autophagy. This suggests a new role for endosomal heparanase in exposing this cryptic motif present in the initial large heparin chains on serglycin and in the highly sulfated (NS) domains of heparan sulfate.

Indexed as

AnimalsAutophagyCell DivisionDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1EndosomesExtracellular MatrixGene ExpressionGlucuronidaseHeparanaseHeparan SulfateHeparinHumansHyaluronic AcidMast CellsMesangial CellsGlucuronidaseHeparanaseHeparan SulfateHeparinHyaluronic AcidProteoglycansReceptors, Cell SurfaceserglycinVesicular Transport ProteinsHeparanaseHeparan sulfateHeparinHeparitinaseHyaluronan

Identifiers

PMID25892563
PMCPMC9701091
OpenAlexW2025036409

What OpenQuestion holds

Textmetadata
LicenceTDM
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.