Evidence map›Paper›PMID 28177139›Full record

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

Canalization Leads to Similar Whole Bone Mechanical Function at Maturity in Two Inbred Strains of Mice.

Stephen H Schlecht, Lauren M Smith, Melissa A Ramcharan, Erin Mr Bigelow, Bonnie T Nolan, Noah J Mathis, Amber Cathey, Eugene Manley, Rajasree Menon, Richard C McEachin 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, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. State of the mineralized tissue comprising the femoral ACL enthesis in young women with an ACL failure.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2022
    Article
  4. Article
  5. Morphology of Mouse Anterior Cruciate Ligament-Complex Changes Following Exercise During Pubertal Growth.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2019
    Article
  6. Article
  7. 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

12 authors at 4 institutions in 2 countries.

Stephen H SchlechtDepartment of Orthopaedic Surgery, University of Michigan, Ann Arbor, MI, USA.
Lauren M SmithSchool of Public Health, University of Michigan, Ann Arbor, MI, USA.
Melissa A RamcharanDepartment of Orthopaedic Surgery, University of Michigan, Ann Arbor, MI, USA.
Erin Mr BigelowDepartment of Orthopaedic Surgery, University of Michigan, Ann Arbor, MI, USA.
Bonnie T NolanDepartment of Orthopaedic Surgery, University of Michigan, Ann Arbor, MI, USA.
Noah J MathisDepartment of Orthopaedic Surgery, University of Michigan, Ann Arbor, MI, USA.
Amber CatheySchool of Public Health, University of Michigan, Ann Arbor, MI, USA.
Eugene ManleyDepartment of Cell, Developmental, and Cancer Biology, Oregon Health and Science University, Portland, OR, USA.
Rajasree MenonDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI, USA.
Richard C McEachinDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI, USA.
Joseph H NadeauPacific Northwest Diabetes Research Institute, Seattle, WA, USA.
Karl J JepsenDepartment of Orthopaedic Surgery, University of Michigan, Ann Arbor, MI, USA.
University of Michigan–Ann Arbor · USAlliance Bioversity International - CIAT · ITPacific Northwest Diabetes Research Institute · USThe University of Texas System · US

Funding

Tissue Engineering and RegenerationT32DE007057 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID H. KOHN · 1985 to 2026
$17.3M
Structure, Composition, & Histology Core - Core BP30AR069620 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KARL J JEPSEN · 2016 to 2026
$8.4M
GENETIC DETERMINATION OF SKELETAL FRAGILITYR01AR044927 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JEPSEN, KARL J · 2002 to 2014
$4.3M
Phoenix / X-ray nanoTOMS10RR026336 · NCRR · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI JEPSEN, KARL J · 2011 to 2011
$562k
NCRR NIH HHS S10 RR026336NIAMS NIH HHS P30 AR069620NIAMS NIH HHS R01 AR044927NIDCR NIH HHS T32 DE007057
6 · The paper itself

Abstract

Previously, we showed that cortical mineralization is coordinately adjusted to mechanically offset external bone size differences between A/J (narrow) and C57BL/6J (wide) mouse femora to achieve whole bone strength equivalence at adulthood. The identity of the genes and their interactions that are responsible for establishing this homeostatic state (ie, canalization) remain unknown. We hypothesize that these inbred strains, whose interindividual differences in bone structure and material properties mimic that observed among humans, achieve functional homeostasis by differentially adjusting key molecular pathways regulating external bone size and mineralization throughout growth. The cortices of A/J and C57BL/6J male mouse femora were phenotyped and gene expression levels were assessed across growth (ie, ages 2, 4, 6, 8, 12, 16 weeks). A difference in total cross-sectional area (p < 0.01) and cortical tissue mineral density were apparent between mouse strains by age 2 weeks and maintained at adulthood (p < 0.01). These phenotypic dissimilarities corresponded to gene expression level differences among key regulatory pathways throughout growth. A/J mice had a 1.55- to 7.65-fold greater expression among genes inhibitory to Wnt pathway induction, whereas genes involved in cortical mineralization were largely upregulated 1.50- to 3.77-fold to compensate for their narrow diaphysis. Additionally, both mouse strains showed an upregulation among Wnt pathway antagonists corresponding to the onset of adult ambulation (ie, increased physiological loads). This contrasts with other studies showing an increase in Wnt pathway activation after functionally isolated, experimental in vivo loading regimens. A/J and C57BL/6J long bones provide a model to develop a systems-based approach to identify individual genes and the gene-gene interactions that contribute to trait differences between the strains while being involved in the process by which these traits are coordinately adjusted to establish similar levels of mechanical function, thus providing insight into the process of canalization. © 2017 American Society for Bone and Mineral Research.

Indexed as

Stress, MechanicalAnimalsBone DensityEpistasis, GeneticFemurGene Expression RegulationHumansMiceSpecies SpecificityWnt Signaling PathwayBONECANALIZATIONFUNCTIONHOMEOSTASISWNT/Β-CATENIN PATHWAY

Identifiers

PMID28177139
PMCPMC5413428
OpenAlexW2587366947

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.