Evidence map›Paper›PMID 38223929›Full record

ArticleAmerican journal of physiology. Cell physiology2024

The ecto-nucleotide pyrophosphatase/phosphodiesterase 2 promotes early osteoblast differentiation and mineralization in stromal stem cells.

Irina L Tourkova, Quitterie C Larrouture, Silvia Liu, Jianhua Luo, Paul H Schlesinger, Harry C Blair

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
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

6 authors at 2 institutions in 1 country.

Irina L TourkovaResearch Service, VA Medical Centre, Pittsburgh, Pennsylvania, United States.
Quitterie C LarroutureDepartment of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States.
Silvia LiuDepartment of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States.
Jianhua LuoDepartment of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States.
Paul H SchlesingerDepartment of Cell Biology, Washington University, St. Louis, Missouri, United States.
Harry C BlairResearch Service, VA Medical Centre, Pittsburgh, Pennsylvania, United States.ORCID 0000-0002-1152-3718
University of Pittsburgh · USWashington University in St. Louis · US

Funding

Epithelial Osteoblast Function: The Role of Acid TransportR01AR076146 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BLAIR, HARRY COLBERT, NELSON, DEBORAH J. · 2020 to 2024
$2.6M
Regulation of Osteoblasts by ACTH and VEGFI01BX002490 · VA · VETERANS HEALTH ADMINISTRATION · PI BLAIR, HARRY COLBERT · 2015 to 2025
–
BLRD VA I01 BX002490HHS | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) R01 AR076146-01NIAMS NIH HHS R01 AR076146U.S. Department of Veterans Affairs (VA) BX002490-06A1
6 · The paper itself

Abstract

The phosphodiesterase enzymes mediate calcium-phosphate deposition in various tissues, although which enzymes are active in bone mineralization is unclear. Using gene array analysis, we found that a member of ecto-nucleotide pyrophosphatase/phosphodiesterase family, ENPP2, was strongly down-regulated with age in stromal stem cells that produce osteoblasts and make bone. This is in keeping with reduced bone formation in older animals. Thus, we hypothesized that ENPP2 is, at least in part, an early mediator of bone formation and thus may reflect reduced bone formation with age. Since ENPP2 has not previously been shown to have a role in osteoblast differentiation, we studied its effect on bone differentiation from stromal stem cells, verified by flow cytometry for stem cell antigens. In these remarkably uniform osteoblast precursors, we did transfection with ENPP2 DsiRNA, scrambled DsiRNA, or no transfection to make cells with normal or greatly reduced ENPP2 and analyzed osteoblast differentiation and mineralization. Osteoblast differentiation down-regulation was shown by alizarin red binding, silver staining, and alkaline phosphatase activity. Differences were confirmed by real-time PCR for alkaline phosphatase (ALPL), osteocalcin (BGLAP), and ENPP2 and by Western Blot for Enpp2. These were decreased, ∼50%, in osteoblasts transfected with ENPP2 DsiRNA compared with cells transfected with a scrambled DsiRNA or not transfected (control) cells. This finding is the first evidence for the role of ENPP2 in osteoblast differentiation and mineralization.

Indexed as

CalcinosisOsteogenesisPyrophosphatasesAlkaline PhosphataseAnimalsCell DifferentiationPhosphoric Diester HydrolasesAlkaline Phosphatasenucleotide pyrophosphatasePhosphoric Diester HydrolasesPyrophosphatasesbone mineralizationecto-nucleotide pyrophosphatase/phosphodiesterase 2osteoblastosteoblast differentiationstromal stem cell

Identifiers

PMID38223929
PMCPMC11193479
OpenAlexW4390885438

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.