Evidence map›Paper›PMID 33305372›Full record

ArticleJournal of cellular physiology2021

Osteoblast-specific deficiency of ectonucleotide pyrophosphatase or phosphodiesterase-1 engenders insulin resistance in high-fat diet fed mice.

Fiona L Roberts, Nabil A Rashdan, Kanchan Phadwal, Greg R Markby, Scott Dillon, Janna Zoll, Julian Berger, Elspeth Milne, Isabel R Orriss, Gerard Karsenty and 4 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of cellular physiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Bone mineralisation and glucose metabolism.Current opinion in endocrine and metabolic research · 2023
    Review
  5. Review
  6. ENPP1's regulation of extracellular cGAMP is a ubiquitous mechanism of attenuating STING signaling.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  7. Article
  8. Article
  9. Regulatory Role of Sex Hormones in Cardiovascular Calcification.International journal of molecular sciences · 2021
    Review
  10. Article
  11. 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

14 authors at 5 institutions in 2 countries.

Fiona L RobertsFunctional Genetics and Development, The Royal (Dick) School of Veterinary Studies and The Roslin Institute, University of Edinburgh, Midlothian, UK.ORCID 0000-0001-9111-9194
Nabil A RashdanFunctional Genetics and Development, The Royal (Dick) School of Veterinary Studies and The Roslin Institute, University of Edinburgh, Midlothian, UK.
Kanchan PhadwalFunctional Genetics and Development, The Royal (Dick) School of Veterinary Studies and The Roslin Institute, University of Edinburgh, Midlothian, UK.ORCID 0000-0001-6745-9818
Greg R MarkbyFunctional Genetics and Development, The Royal (Dick) School of Veterinary Studies and The Roslin Institute, University of Edinburgh, Midlothian, UK.
Scott DillonFunctional Genetics and Development, The Royal (Dick) School of Veterinary Studies and The Roslin Institute, University of Edinburgh, Midlothian, UK.
Janna ZollDepartment of Cell and Molecular Biology, John A. Burns School of Medicine, University of Hawaii at Manoa, Honolulu, Hawaii, USA.
Julian BergerDepartment of Genetics and Development, Columbia University Medical Center, New York, New York, USA.
Elspeth MilneFunctional Genetics and Development, The Royal (Dick) School of Veterinary Studies and The Roslin Institute, University of Edinburgh, Midlothian, UK.
Isabel R OrrissDepartment of Comparative Biomedical Sciences, The Royal Veterinary College, London, UK.
Gerard KarsentyDepartment of Genetics and Development, Columbia University Medical Center, New York, New York, USA.
Olivier Le SauxDepartment of Cell and Molecular Biology, John A. Burns School of Medicine, University of Hawaii at Manoa, Honolulu, Hawaii, USA.
Nicholas M MortonCentre for Cardiovascular Science, The Queen's Medical Research Institute, The College of Medicine and Veterinary Medicine, The University of Edinburgh, Edinburgh, UK.
Colin FarquharsonFunctional Genetics and Development, The Royal (Dick) School of Veterinary Studies and The Roslin Institute, University of Edinburgh, Midlothian, UK.
Vicky E MacRaeFunctional Genetics and Development, The Royal (Dick) School of Veterinary Studies and The Roslin Institute, University of Edinburgh, Midlothian, UK.
Roslin Institute · GBColumbia University Irving Medical Center · USUniversity of Hawaiʻi at Mānoa · USRoyal Veterinary College · GBThe Queen's Medical Research Institute · GB

Funding

TRPA1 Physiology in Diabetes, Metabolic Syndrome, and MetabolismP20GM113134 · NIGMS · UNIVERSITY OF HAWAII AT MANOA · PI Michael A. Ortega · 2017 to 2026
$21.5M
Biotechnology and Biological Sciences Research Council BB/J004316/1;BBS/E/D/20221657;BB/P02503X/1Biotechnology and Biological Sciences Research Council BBS/E/R/00003741British Heart Foundation PG/15/13/31296NIGMS NIH HHS P20 GM113134
6 · The paper itself

Abstract

Supraphysiological levels of the osteoblast-enriched mineralization regulator ectonucleotide pyrophosphatase or phosphodiesterase-1 (NPP1) is associated with type 2 diabetes mellitus. We determined the impact of osteoblast-specific Enpp1 ablation on skeletal structure and metabolic phenotype in mice. Female, but not male, 6-week-old mice lacking osteoblast NPP1 expression (osteoblast-specific knockout [KO]) exhibited increased femoral bone volume or total volume (17.50% vs. 11.67%; p < .01), and reduced trabecular spacing (0.187 vs. 0.157 mm; p < .01) compared with floxed (control) mice. Furthermore, an enhanced ability of isolated osteoblasts from the osteoblast-specific KO to calcify their matrix in vitro compared to fl/fl osteoblasts was observed (p < .05). Male osteoblast-specific KO and fl/fl mice showed comparable glucose and insulin tolerance despite increased levels of insulin-sensitizing under-carboxylated osteocalcin (195% increase; p < .05). However, following high-fat-diet challenge, osteoblast-specific KO mice showed impaired glucose and insulin tolerance compared with fl/fl mice. These data highlight a crucial local role for osteoblast NPP1 in skeletal development and a secondary metabolic impact that predominantly maintains insulin sensitivity.

Indexed as

Insulin ResistanceOsteogenesisAnimalsBiomarkersBlood GlucoseBone and BonesCancellous BoneCells, CulturedDiet, High-FatDisease Models, AnimalFemaleFemurInsulinMaleMiceMice, KnockoutBiomarkersBlood Glucoseectonucleotide pyrophosphatase phosphodiesterase 1InsulinOsteocalcinPhosphoric Diester HydrolasesPyrophosphatasesbone-fat interactionsgenetic animal modelsmatrix mineralizationnon-collagenous proteinsosteoblasts

Identifiers

PMID33305372
PMCPMC9665351
OpenAlexW3111671508

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.