Evidence map›Paper›PMID 27085457›Full record

ArticleBone2016

Parallel mechanisms suppress cochlear bone remodeling to protect hearing.

Emmanuel J Jáuregui, Omar Akil, Claire Acevedo, Faith Hall-Glenn, Betty S Tsai, Hrishikesh A Bale, Ellen Liebenberg, Mary Beth Humphrey, Robert O Ritchie, Lawrence R Lustig and 1 more

Abstract 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 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Transcriptome Profiling of Osteoblasts in a Medaka (Frontiers in cell and developmental biology · 2022
    Article
  7. Article
  8. Poor bone matrix quality: What can be done about it?Current osteoporosis reports · 2021
    Review
  9. Hypermineralization of Hearing-Related Bones by a Specific Osteoblast Subtype.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2021
    Article
  10. Article
  11. Article
  12. Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  13. YAP and TAZ Mediate Osteocyte Perilacunar/Canalicular Remodeling.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2020
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Neural crest and the origin of species-specific pattern.Genesis (New York, N.Y. : 2000) · 2018
    Review
  20. 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 3 institutions in 1 country.

Emmanuel J JáureguiDepartment of Orthopaedic Surgery, University of California, San Francisco, United States.
Omar AkilDepartment of Otolaryngology-Head & Neck Surgery, University of California, San Francisco, United States.
Claire AcevedoDepartment of Orthopaedic Surgery, University of California, San Francisco, United States; Materials Science Division, Lawrence Berkeley National Laboratory, Berkeley, CA, United States.
Faith Hall-GlennDepartment of Orthopaedic Surgery, University of California, San Francisco, United States.
Betty S TsaiDepartment of Otorhinolaryngology, University of Oklahoma Health Sciences Center, United States.
Hrishikesh A BaleMaterials Science Division, Lawrence Berkeley National Laboratory, Berkeley, CA, United States.
Ellen LiebenbergDepartment of Orthopaedic Surgery, University of California, San Francisco, United States.
Mary Beth HumphreyDepartment of Medicine, University of Oklahoma Health Sciences Center, United States.
Robert O RitchieMaterials Science Division, Lawrence Berkeley National Laboratory, Berkeley, CA, United States.
Lawrence R LustigDepartment of Otolaryngology-Head & Neck Surgery, University of California, San Francisco, United States.
Tamara AllistonDepartment of Orthopaedic Surgery, University of California, San Francisco, United States; Department of Otolaryngology-Head & Neck Surgery, University of California, San Francisco, United States. Electronic address: tamara.alliston@ucsf.edu.
University of California, San Francisco · USLawrence Berkeley National Laboratory · USUniversity of Oklahoma Health Sciences Center · US

Funding

The mechanistic control of bone quality and joint crosstalk by osteocytesR01DE019284 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HERNANDEZ, CHRISTOPHER JOHN · 2009 to 2024
$7.6M
UCSF Core Center for Musculoskeletal Biology and MedicineP30AR066262 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MAJUMDAR, SHARMILA · 2014 to 2018
$3.0M
TGF-Beta regulation of Runx2 in bone formation and qualityR03DE016868 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ALLISTON, TAMARA N · 2006 to 2007
$151k
NIAMS NIH HHS P30 AR066262NIDCR NIH HHS R01 DE019284NIDCR NIH HHS R03 DE016868
6 · The paper itself

Abstract

Bone remodeling, a combination of bone resorption and formation, requires precise regulation of cellular and molecular signaling to maintain proper bone quality. Whereas osteoblasts deposit and osteoclasts resorb bone matrix, osteocytes both dynamically resorb and replace perilacunar bone matrix. Osteocytes secrete proteases like matrix metalloproteinase-13 (MMP13) to maintain the material quality of bone matrix through perilacunar remodeling (PLR). Deregulated bone remodeling impairs bone quality and can compromise hearing since the auditory transduction mechanism is within bone. Understanding the mechanisms regulating cochlear bone provides unique ways to assess bone quality independent of other aspects that contribute to bone mechanical behavior. Cochlear bone is singular in its regulation of remodeling by expressing high levels of osteoprotegerin. Since cochlear bone expresses a key PLR enzyme, MMP13, we examined whether cochlear bone relies on, or is protected from, osteocyte-mediated PLR to maintain hearing and bone quality using a mouse model lacking MMP13 (MMP13(-/-)). We investigated the canalicular network, collagen organization, lacunar volume via micro-computed tomography, and dynamic histomorphometry. Despite finding defects in these hallmarks of PLR in MMP13(-/-) long bones, cochlear bone revealed no differences in these markers, nor hearing loss as measured by auditory brainstem response (ABR) or distortion product oto-acoustic emissions (DPOAEs), between wild type and MMP13(-/-) mice. Dynamic histomorphometry revealed abundant PLR by tibial osteocytes, but near absence in cochlear bone. Cochlear suppression of PLR corresponds to repression of several key PLR genes in the cochlea relative to long bones. These data suggest that cochlear bone uniquely maintains bone quality and hearing independent of MMP13-mediated osteocytic PLR. Furthermore, the cochlea employs parallel mechanisms to inhibit remodeling by osteoclasts and osteoblasts, and by osteocytes, to protect hearing. Understanding the cellular and molecular mechanisms that confer site-specific control of bone remodeling has the potential to elucidate new pathways that are deregulated in skeletal disease.

Indexed as

AnimalsBone RemodelingCochleaHearingMatrix Metalloproteinase 13MiceMice, KnockoutX-Ray MicrotomographyMatrix Metalloproteinase 13Mmp13 protein, mouseBone matrixBone remodelingCollagenMatrix mineralizationMouse modelOsteocytesPerilacunar remodeling

Identifiers

PMID27085457
PMCPMC4916019
OpenAlexW2341830711

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.