Evidence map›Paper›PMID 27704638›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2017

Control of Bone Anabolism in Response to Mechanical Loading and PTH by Distinct Mechanisms Downstream of the PTH Receptor.

Jesus Delgado-Calle, Xiaolin Tu, Rafael Pacheco-Costa, Kevin McAndrews, Rachel Edwards, Gretel G Pellegrini, Kali Kuhlenschmidt, Naomie Olivos, Alexander Robling, Munro Peacock and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

65 citing papers in PubMed, 106 citations in OpenAlex.

  1. Gender-Affirming Hormone Treatment Decreases Bone Turnover in Transwomen and Older Transmen.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2019
    Trial
  2. Article
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  7. Advances in Parathyroid Hormone-based medicines.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2025
    Review
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  20. Osteocyte Estrogen Receptor β (Ot-ERβ) Regulates Bone Turnover and Skeletal Adaptive Response to Mechanical Loading Differently in Male and Female Growing and Adult Mice.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2023
    Article

5 more citing papers are in PubMed but not listed here.

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.

Jesus Delgado-CalleDepartment of Anatomy and Cell Biology, School of Medicine, Indiana University, Indianapolis, IN, USA.
Xiaolin TuDepartment of Anatomy and Cell Biology, School of Medicine, Indiana University, Indianapolis, IN, USA.
Rafael Pacheco-CostaDepartment of Anatomy and Cell Biology, School of Medicine, Indiana University, Indianapolis, IN, USA.
Kevin McAndrewsDepartment of Anatomy and Cell Biology, School of Medicine, Indiana University, Indianapolis, IN, USA.
Rachel EdwardsDepartment of Anatomy and Cell Biology, School of Medicine, Indiana University, Indianapolis, IN, USA.
Gretel G PellegriniDepartment of Anatomy and Cell Biology, School of Medicine, Indiana University, Indianapolis, IN, USA.
Kali KuhlenschmidtDepartment of Anatomy and Cell Biology, School of Medicine, Indiana University, Indianapolis, IN, USA.
Naomie OlivosDepartment of Anatomy and Cell Biology, School of Medicine, Indiana University, Indianapolis, IN, USA.
Alexander RoblingDepartment of Anatomy and Cell Biology, School of Medicine, Indiana University, Indianapolis, IN, USA.
Munro PeacockDepartment of Medicine, Division of Endocrinology, School of Medicine, Indiana University, Indianapolis, IN, USA.
Lilian I PlotkinDepartment of Anatomy and Cell Biology, School of Medicine, Indiana University, Indianapolis, IN, USA.
Teresita BellidoDepartment of Anatomy and Cell Biology, School of Medicine, Indiana University, Indianapolis, IN, USA.
Indiana University – Purdue University Indianapolis · USRichard L. Roudebush VA Medical Center · USIndiana University Indianapolis

Funding

Short-Term Training Program In Biomedical SciencesT35HL110854 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI Brittney-Shea Herbert, Catherine Rufatto Sears · 2012 to 2026
$3.4M
Glucocorticoid-induced Atrophy in Bone and MuscleR01AR059357 · NIAMS · UNIV OF ARKANSAS FOR MED SCIS · PI BELLIDO, TERESITA M. · 2011 to 2022
$3.4M
PTH receptor Signaling and Diabetes-induced Bone DiseaseI01BX002104 · VA · RLR VA MEDICAL CENTER · PI BELLIDO, TERESITA M. · 2014 to 2023
–
BLRD VA I01 BX002104BLRD VA IK6 BX004596NHLBI NIH HHS T35 HL110854NIAMS NIH HHS R01 AR059357
6 · The paper itself

Abstract

Osteocytes integrate the responses of bone to mechanical and hormonal stimuli by poorly understood mechanisms. We report here that mice with conditional deletion of the parathyroid hormone (PTH) receptor 1 (Pth1r) in dentin matrix protein 1 (DMP1)-8kb-expressing cells (cKO) exhibit a modest decrease in bone resorption leading to a mild increase in cancellous bone without changes in cortical bone. However, bone resorption in response to endogenous chronic elevation of PTH in growing or adult cKO mice induced by a low calcium diet remained intact, because the increased bone remodeling and bone loss was indistinguishable from that exhibited by control littermates. In contrast, the bone gain and increased bone formation in cancellous and cortical bone induced by daily injections of PTH and the periosteal bone apposition induced by axial ulna loading were markedly reduced in cKO mice compared to controls. Remarkably, however, wild-type (WT) control littermates and transgenic mice overexpressing SOST injected daily with PTH exhibit similar activation of Wnt/β-catenin signaling, increased bone formation, and cancellous and cortical bone gain. Taken together, these findings demonstrate that Pth1r in DMP1-8kb-expressing cells is required to maintain basal levels of bone resorption but is dispensable for the catabolic action of chronic PTH elevation; and it is essential for the anabolic actions of daily PTH injections and mechanical loading. However, downregulation of Sost/sclerostin, previously shown to be required for bone anabolism induced by mechanical loading, is not required for PTH-induced bone gain, showing that other mechanisms downstream of the Pth1r in DMP1-8kb-expressing cells are responsible for the hormonal effect. © 2016 American Society for Bone and Mineral Research.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsBone and BonesBone RemodelingBone ResorptionDown-RegulationExtracellular Matrix ProteinsFibroblast Growth Factor-23Gene DeletionGlycoproteinsIntercellular Signaling Peptides and ProteinsMice, Inbred C57BLMice, KnockoutModels, BiologicalOrgan SizeOsteocytesAdaptor Proteins, Signal TransducingDmp1 protein, mouseExtracellular Matrix ProteinsFgf23 protein, mouseFibroblast Growth Factor-23GlycoproteinsIntercellular Signaling Peptides and ProteinsParathyroid HormoneReceptor, Parathyroid Hormone, Type 1Sost protein, mouseGENETIC ANIMAL MODELSMOLECULAR PATHWAYS-REMODELINGOSTEOCYTESPTH/VITD/FGF23WNT/Β-CATENIN/LRPS

Identifiers

PMID27704638
PMCPMC8502039
OpenAlexW2528107193

What OpenQuestion holds

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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.