Evidence map›Paper›PMID 29175363›Full record

ArticleJournal of structural biology2018

Bone morphogenetic protein signaling through ACVR1 and BMPR1A negatively regulates bone mass along with alterations in bone composition.

Ce Shi, Gurjit S Mandair, Honghao Zhang, Gloria G Vanrenterghem, Ryan Ridella, Akira Takahashi, Yanshuai Zhang, David H Kohn, Michael D Morris, Yuji Mishina and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of structural biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. [Latest Research Findings on the Regulation of Bone Homeostasis by ALK3].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. External Bone Size Is a Key Determinant of Strength-Decline Trajectories of Aging Male Radii.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2019
    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

11 authors at 2 institutions in 2 countries.

Ce ShiDepartment of Oral Pathology, School and Hospital of Stomatology, Jilin University, 1500 Qinghua Road, Changchun 130000, China; Department of Biologic and Materials Sciences, University of Michigan, School of Dentistry, 1011 N. University Avenue, Ann Arbor, MI 48109-1078, USA. Electronic address: ceshi@jlu.edu.cn.
Gurjit S MandairDepartment of Biologic and Materials Sciences, University of Michigan, School of Dentistry, 1011 N. University Avenue, Ann Arbor, MI 48109-1078, USA. Electronic address: gmandair@umich.edu.
Honghao ZhangDepartment of Biologic and Materials Sciences, University of Michigan, School of Dentistry, 1011 N. University Avenue, Ann Arbor, MI 48109-1078, USA. Electronic address: zhangho@umich.edu.
Gloria G VanrenterghemDepartment of Biologic and Materials Sciences, University of Michigan, School of Dentistry, 1011 N. University Avenue, Ann Arbor, MI 48109-1078, USA. Electronic address: ggracevr@umich.edu.
Ryan RidellaDepartment of Chemistry, University of Michigan, 930 N. University Avenue, Ann Arbor, MI 48108-1055, USA.
Akira TakahashiDepartment of Biologic and Materials Sciences, University of Michigan, School of Dentistry, 1011 N. University Avenue, Ann Arbor, MI 48109-1078, USA. Electronic address: taakira@umich.edu.
Yanshuai ZhangDepartment of Biologic and Materials Sciences, University of Michigan, School of Dentistry, 1011 N. University Avenue, Ann Arbor, MI 48109-1078, USA. Electronic address: yanshuaizhang2004@163.com.
David H KohnDepartment of Biologic and Materials Sciences, University of Michigan, School of Dentistry, 1011 N. University Avenue, Ann Arbor, MI 48109-1078, USA; Biomedical Engineering College of Engineering, University of Michigan, MI 48109-2110, USA. Electronic address: dhkohn@umich.edu.
Michael D MorrisDepartment of Chemistry, University of Michigan, 930 N. University Avenue, Ann Arbor, MI 48108-1055, USA. Electronic address: mdmorris@umich.edu.
Yuji MishinaDepartment of Biologic and Materials Sciences, University of Michigan, School of Dentistry, 1011 N. University Avenue, Ann Arbor, MI 48109-1078, USA. Electronic address: mishina@umich.edu.
Hongchen SunDepartment of Oral Pathology, School and Hospital of Stomatology, Jilin University, 1500 Qinghua Road, Changchun 130000, China. Electronic address: hcsun@mail.jlu.edu.cn.
University of Michigan–Ann Arbor · USJilin University · CN

Funding

Structure, Composition, & Histology Core - Core BP30AR069620 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KARL J JEPSEN · 2016 to 2026
$8.4M
Molecular pathogenesis of craniosynostosis caused by enhanced BMP signalingR01DE020843 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MISHINA, YUJI · 2010 to 2019
$4.9M
The design, development and evaluation of a nano/micro filled novel "smart" dentaU01DE023771 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CLARKSON, BRIAN H, SCOTT, TIMOTHY FRANCIS · 2013 to 2017
$2.6M
MicroCT 100S10RR026475 · NCRR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KOHN, DAVID H. · 2010 to 2010
$381k
NCRR NIH HHS S10 RR026475NIAMS NIH HHS P30 AR069620NIDCR NIH HHS R01 DE020843NIDCR NIH HHS U01 DE023771
6 · The paper itself

Abstract

Bone quantity and bone quality are important factors in determining the properties and the mechanical functions of bone. This study examined the effects of disrupting bone morphogenetic protein (BMP) signaling through BMP receptors on bone quantity and bone quality. More specifically, we disrupted two BMP receptors, Acvr1 and Bmpr1a, respectively, in Osterix-expressing osteogenic progenitor cells in mice. We examined the structural changes to the femora from 3-month old male and female conditional knockout (cKO) mice using micro-computed tomography (micro-CT) and histology, as well as compositional changes to both cortical and trabecular compartments of bone using Raman spectroscopy. We found that the deletion of Acvr1 and Bmpr1a, respectively, in an osteoblast-specific manner resulted in higher bone mass in the trabecular compartment. Disruption of Bmpr1a resulted in a more significantly increased bone mass in the trabecular compartment. We also found that these cKO mice showed lower mineral-to-matrix ratio, while tissue mineral density was lower in the cortical compartment. Collagen crosslink ratio was higher in both cortical and trabecular compartments of male cKO mice. Our study suggested that BMP signaling in osteoblast mediated by BMP receptors, namely ACVR1 and BMPR1A, is critical in regulating bone quantity and bone quality.

Indexed as

Activin Receptors, Type IAnimalsBone DensityBone Morphogenetic Protein Receptors, Type ICancellous BoneCollagenFemaleFemurMaleMice, KnockoutOsteoblastsSignal TransductionSpectrum Analysis, RamanX-Ray MicrotomographyActivin Receptors, Type IAcvr1 protein, mouseBmpr1a protein, mouseBone Morphogenetic Protein Receptors, Type ICollagenBMP receptorBone compositionBone qualityBone quantityMicro-CTRaman spectroscopy

Identifiers

PMID29175363
PMCPMC5820174
OpenAlexW2771054454

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.