Evidence map›Paper›PMID 27113527›Full record

ArticleBone2016

Removing or truncating connexin 43 in murine osteocytes alters cortical geometry, nanoscale morphology, and tissue mechanics in the tibia.

Max A Hammond, Alycia G Berman, Rafael Pacheco-Costa, Hannah M Davis, Lilian I Plotkin, Joseph M Wallace

Open access · greenAbstract read
In one paragraph

Article in Bone, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
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  8. Article
  9. Pro-inflammatory Cytokines and Osteocytes.Current osteoporosis reports · 2019
    Review
  10. Article
  11. Article
  12. Connexin43 and Runx2 Interact to Affect Cortical Bone Geometry, Skeletal Development, and Osteoblast and Osteoclast Function.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2017
    Article
  13. Article
  14. Article
  15. Review
  16. Article
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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 4 institutions in 1 country.

Max A HammondWeldon School of Biomedical Engineering, Purdue University, West Lafayette, IN, United States.
Alycia G BermanDepartment of Biomedical Engineering, Indiana University-Purdue University at Indianapolis, IN, United States.
Rafael Pacheco-CostaDepartment of Anatomy and Cell Biology, Indiana University School of Medicine, IN, United States.
Hannah M DavisDepartment of Anatomy and Cell Biology, Indiana University School of Medicine, IN, United States.
Lilian I PlotkinDepartment of Anatomy and Cell Biology, Indiana University School of Medicine, IN, United States; Roudebush Veterans Administration Medical Center, Indianapolis, IN, United States.
Joseph M WallaceDepartment of Biomedical Engineering, Indiana University-Purdue University at Indianapolis, IN, United States; Department of Orthopaedic Surgery, Indiana University School of Medicine, IN, United States. Electronic address: jmwalla@iupui.edu.
Indiana University School of MedicineIndiana University – Purdue University Indianapolis · USPurdue University West Lafayette · USRichard L. Roudebush VA Medical Center · US

Funding

Osteocyte Apoptosis and Regulation of Bone Resorption with AgingR01AR067210 · NIAMS · INDIANA UNIVERSITY INDIANAPOLIS · PI PLOTKIN, LILIAN IRENE · 2015 to 2019
$1.9M
Connexin 43 Hemichannels and Signaling In BoneR01AR053643 · NIAMS · INDIANA UNIVERSITY INDIANAPOLIS · PI PLOTKIN, LILIAN IRENE · 2008 to 2012
$1.6M
NIAMS NIH HHS R01 AR053643NIAMS NIH HHS R01 AR067210
6 · The paper itself

Abstract

Gap junctions are formed from ubiquitously expressed proteins called connexins that allow the transfer of small signaling molecules between adjacent cells. Gap junctions are especially important for signaling between osteocytes and other bone cell types. The most abundant type of connexin in bone is connexin 43 (Cx43). The C-terminal domain of Cx43 is thought to be an important modulator of gap junction function but the role that this domain plays in regulating tissue-level mechanics is largely unknown. We hypothesized that the lack of the C-terminal domain of Cx43 would cause morphological and compositional changes as well as differences in how bone responds to reference point indentation (RPI) and fracture toughness testing. The effects of the C-terminal domain of Cx43 in osteocytes and other cell types were assessed in a murine model (C57BL/6 background). Mice with endogenous Cx43 in their osteocytes removed via a Cre-loxP system were crossed with knock-in mice which expressed Cx43 that lacked the C-terminal domain in all cell types due to the insertion of a truncated allele to produce the four groups used in the study. The main effect of removing the C-terminal domain from osteocytic Cx43 increased cortical mineral crystallinity (p=0.036) and decreased fracture toughness (p=0.017). The main effect of the presence of the C-terminal domain in other cell types increased trabecular thickness (p<0.001), cortical thickness (p=0.008), and average RPI unloading slope (p=0.004). Collagen morphology was altered when either osteocytes lacked Cx43 (p=0.008) or some truncated Cx43 was expressed in all cell types (p<0.001) compared to controls but not when only the truncated form of Cx43 was expressed in osteocytes (p=0.641). In conclusion, the presence of the C-terminal domain of Cx43 in osteocytes and other cell types is important to maintain normal structure and mechanical integrity of bone.

Indexed as

AnimalsBiomechanical PhenomenaCancellous BoneConnexin 43Cortical BoneDiaphysesMiceMicroscopy, Atomic ForceNanoparticlesOsteocytesSpectrum Analysis, RamanTibiaTibial FracturesConnexin 43Atomic force microscopyBoneFracture toughnessRaman spectroscopyReference point indentationType I collagen

Identifiers

PMID27113527
PMCPMC4899203
OpenAlexW2340951780

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.