Evidence map›Paper›PMID 26740471›Full record

ReviewSeminars in cell & developmental biology2016

Connexins in the skeleton.

Joseph P Stains, Roberto Civitelli

Abstract readReview
In one paragraph

Review in Seminars in cell & developmental biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.2field-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

34 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Evolution and Spatiotemporal Expression ofJournal of developmental biology · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Connexin 43 Hemichannels Regulate Osteoblast to Osteocyte Differentiation.Frontiers in cell and developmental biology · 2022
    Article
  12. ATP transporters in the joints.Purinergic signalling · 2021
    Review
  13. The diverse origin of bone-forming osteoblasts.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2021
    Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Conditional Activation of NF-κB Inducing Kinase (NIK) in the Osteolineage Enhances Both Basal and Loading-Induced Bone Formation.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2019
    Article
  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

2 authors at 2 institutions in 1 country.

Joseph P StainsDepartment of Orthopaedics, University of Maryland, School of Medicine, Baltimore, MD, United States.
Roberto CivitelliDivision of Bone and Mineral Diseases, Department of Internal Medicine, Washington University in St. Louis, Campus Box 8301, 425 South Euclid, St. Louis, MO 63110, United States. Electronic address: rcivitel@dom.wustl.edu.
University of Maryland, Baltimore · USWashington University in St. Louis · US

Funding

The Role of the Osteoblast Secretome in Bone FormationP30AR057235 · NIAMS · WASHINGTON UNIVERSITY · PI SILVA, MATTHEW J · 2009 to 2018
$5.7M
INTERCELLULAR COMMUNICATION IN BONE CELL PHYSIOLOGYR01AR041255 · NIAMS · WASHINGTON UNIVERSITY · PI CIVITELLI, ROBERTO · 1997 to 2017
$5.3M
Spatial Control of Bone Remodeling by Gap Junction-Communicated cAMPR01AR063631 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI STAINS, JOSEPH P. · 2013 to 2024
$3.3M
Intercellular Signaling in BoneR01AR052719 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI STAINS, JOSEPH P. · 2006 to 2010
$1.3M
INTERCELLULAR COMMUNICATION IN BONE CELL PHYSIOLOGYR29AR041255 · NIAMS · JEWISH HOSPITAL OF SAINT LOUIS · PI CIVITELLI, ROBERTO · 1992 to 1996
–
NIAMS NIH HHS AR041255NIAMS NIH HHS AR052719NIAMS NIH HHS AR063631NIAMS NIH HHS P30 AR057235NIAMS NIH HHS R01 AR041255NIAMS NIH HHS R01 AR052719NIAMS NIH HHS R01 AR063631
6 · The paper itself

Abstract

Shaping of the skeleton (modeling) and its maintenance throughout life (remodeling) require coordinated activity among bone forming (osteoblasts) and resorbing cells (osteoclasts) and osteocytes (bone embedded cells). The gap junction protein connexin43 (Cx43) has emerged as a key modulator of skeletal growth and homeostasis. The skeletal developmental abnormalities present in oculodentodigital and craniometaphyseal dysplasias, both linked to Cx43 gene (GJA1) mutations, demonstrate that the skeleton is a major site of Cx43 action. Via direct action on osteolineage cells, including altering production of pro-osteoclastogenic factors, Cx43 contributes to peak bone mass acquisition, cortical modeling of long bones, and maintenance of bone quality. Cx43 also contributes in diverse ways to bone responsiveness to hormonal and mechanical signals. Skeletal biology research has revealed the complexity of Cx43 function; in addition to forming gap junctions and "hemichannels", Cx43 provides a scaffold for signaling molecules. Hence, Cx43 actively participates in generation and modulation of cellular signals driving skeletal development and homeostasis. Pharmacological interference with Cx43 may in the future help remedy deterioration of bone quality occurring with aging, disuse and hormonal imbalances.

Indexed as

AnimalsBone and BonesBone DevelopmentBone DiseasesConnexinsHomeostasisHumansTranslational Research, BiomedicalConnexinsBoneCx37Cx43Gap junctionSignal transduction

Identifiers

PMID26740471
PMCPMC4779380
OpenAlexW2212384217

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.