Evidence map›Paper›PMID 30882939›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2019

A Novel Osteogenic Cell Line That Differentiates Into GFP-Tagged Osteocytes and Forms Mineral With a Bone-Like Lacunocanalicular Structure.

Kun Wang, Lisa Le, Brad M Chun, LeAnn M Tiede-Lewis, Lora A Shiflett, Matthew Prideaux, Richard S Campos, Patricia A Veno, Yixia Xie, Vladimir Dusevich and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2019. 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
6.4field-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

36 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Isolation, Purification, Generation, and Culture of Osteocytes.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Sclerostin: From Molecule to Clinical Biomarker.International journal of molecular sciences · 2022
    Review
  14. Osteon: Structure, Turnover, and Regeneration.Tissue engineering. Part B, Reviews · 2022
    Review
  15. The osteocyte as a signaling cell.Physiological reviews · 2022
    Review
  16. Connexin 43 Hemichannels Regulate Osteoblast to Osteocyte Differentiation.Frontiers in cell and developmental biology · 2022
    Article
  17. HIF1BioMed research international · 2022
    Article
  18. Article
  19. Osteocytes and Weightlessness.Current osteoporosis reports · 2021
    Review
  20. 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

12 authors at 3 institutions in 1 country.

Kun WangDepartment of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.
Lisa LeDepartment of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.
Brad M ChunDepartment of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.
LeAnn M Tiede-LewisDepartment of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.
Lora A ShiflettDepartment of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.
Matthew PrideauxDepartment of Anatomy and Cell Biology, School of Medicine, Indiana University, Indianapolis, IN, USA.
Richard S CamposDepartment of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.
Patricia A VenoDepartment of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.
Yixia XieDepartment of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.
Vladimir DusevichDepartment of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.
Lynda F BonewaldDepartment of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.
Sarah L DallasDepartment of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.
University of Missouri–Kansas City · USIndiana University Health · USIndiana University – Purdue University Indianapolis · US

Funding

Transgenic and Mechanical Loading CoreP01AG039355 · NIA · UNIVERSITY OF MISSOURI KANSAS CITY · PI BONEWALD, LYNDA F · 2012 to 2024
$19.3M
Leica TCS Sp8 MP Multiphoton MicroscopeS10OD021665 · OD · UNIVERSITY OF MISSOURI KANSAS CITY · PI DALLAS, SARAH L · 2016 to 2016
$600k
Zeiss LSM 710 Confocal Microscopy System for Imaging of Mineralized TissuesS10RR027668 · NCRR · UNIVERSITY OF MISSOURI KANSAS CITY · PI DALLAS, SARAH L · 2011 to 2011
$446k
Extracellular Vesicle Mediated Cell-Cell Communication in BoneR21AR071563 · NIAMS · UNIVERSITY OF MISSOURI KANSAS CITY · PI DALLAS, SARAH L · 2017 to 2018
$377k
Osteocytes as Dynamic CellsR21AR054449 · NIAMS · UNIVERSITY OF MISSOURI KANSAS CITY · PI DALLAS, SARAH L · 2007 to 2008
$340k
NCRR NIH HHS S10 RR027668NIAMS NIH HHS R21 AR054449NIAMS NIH HHS R21 AR071563NIA NIH HHS P01 AG039355NIH HHS S10 OD021665NIH/NIA P01-AG039355NIH/NIAMS R21- AR054449NIH/NIAMS R21-AR071563NIH/Shared Instrumentation Program S10-OD021665NIH/Shared Instrumentation Program S10-RR027668
6 · The paper itself

Abstract

Osteocytes, the most abundant cells in bone, were once thought to be inactive, but are now known to have multifunctional roles in bone, including in mechanotransduction, regulation of osteoblast and osteoclast function and phosphate homeostasis. Because osteocytes are embedded in a mineralized matrix and are challenging to study, there is a need for new tools and cell models to understand their biology. We have generated two clonal osteogenic cell lines, OmGFP66 and OmGFP10, by immortalization of primary bone cells from mice expressing a membrane-targeted GFP driven by the Dmp1-promoter. One of these clones, OmGFP66, has unique properties compared with previous osteogenic and osteocyte cell models and forms 3-dimensional mineralized bone-like structures, containing highly dendritic GFP-positive osteocytes, embedded in clearly defined lacunae. Confocal and electron microscopy showed that structurally and morphologically, these bone-like structures resemble bone in vivo, even mimicking the lacunocanalicular ultrastructure and 3D spacing of in vivo osteocytes. In osteogenic conditions, OmGFP66 cells express alkaline phosphatase (ALP), produce a mineralized type I collagen matrix, and constitutively express the early osteocyte marker, E11/gp38. With differentiation they express osteocyte markers, Dmp1, Phex, Mepe, Fgf23, and the mature osteocyte marker, Sost. They also express RankL, Opg, and Hif1α, and show expected osteocyte responses to PTH, including downregulation of Sost, Dmp1, and Opg and upregulation of RankL and E11/gp38. Live cell imaging revealed the dynamic process by which OmGFP66 bone-like structures form, the motile properties of embedding osteocytes and the integration of osteocyte differentiation with mineralization. The OmGFP10 clone showed an osteocyte gene expression profile similar to OmGFP66, but formed less organized bone nodule-like mineral, similar to other osteogenic cell models. Not only do these cell lines provide useful new tools for mechanistic and dynamic studies of osteocyte differentiation, function, and biomineralization, but OmGFP66 cells have the unique property of modeling osteocytes in their natural bone microenvironment. © 2019 American Society for Bone and Mineral Research.

Indexed as

Cell DifferentiationOsteogenesisAnimalsBiomarkersBone and BonesCell LineExtracellular Matrix ProteinsFibroblast Growth Factor-23Gene Expression RegulationGreen Fluorescent ProteinsMice, TransgenicMineralsModels, BiologicalOsteocytesParathyroid HormoneTime FactorsBiomarkersDmp1 protein, mouseExtracellular Matrix ProteinsFgf23 protein, mouseFibroblast Growth Factor-23Green Fluorescent ProteinsMineralsParathyroid HormoneBONECELL LINEFGF23MINERALIZATIONOSTEOBLASTOSTEOCYTE

Identifiers

PMID30882939
PMCPMC7350928
OpenAlexW2922331472

What OpenQuestion holds

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Registered trials

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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.