Evidence map›Paper›PMID 19277783›Full record

ArticleJournal of the Association for Research in Otolaryngology : JARO2009

Immunocytochemical traits of type IV fibrocytes and their possible relations to cochlear function and pathology.

Joe C Adams

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the Association for Research in Otolaryngology : JARO, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

25 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Kir5.1 channels: potential role in epilepsy and seizure disorders.American journal of physiology. Cell physiology · 2022
    Review
  4. Article
  5. Cochlin Deficiency Protects Aged Mice from Noise-Induced Hearing Loss.International journal of molecular sciences · 2021
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. QTL Mapping of Endocochlear Potential Differences between C57BL/6J and BALB/cJ mice.Journal of the Association for Research in Otolaryngology : JARO · 2016
    Article
  12. Article
  13. Article
  14. Changes in Gene Expression and Hearing Thresholds After Cochlear Implantation.Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology · 2015
    Article
  15. Article
  16. Effects of repeated "benign" noise exposures in young CBA mice: shedding light on age-related hearing loss.Journal of the Association for Research in Otolaryngology : JARO · 2012
    Article
  17. Article
  18. Conditional deletion of calcium-modulating cyclophilin ligand causes deafness in mice.Mammalian genome : official journal of the International Mammalian Genome Society · 2012
    Article
  19. Review
  20. Subcellular distribution and relative expression of fibrocyte markers in the CD/1 mouse cochlea assessed by semiquantitative immunogold electron microscopy.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2011
    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

1 author at 1 institution in 1 country.

Joe C AdamsEaton-Peabody Laboratory, Massachusetts Eye and Ear Infirmary, Boston, MA 02114, USA. Joe_Adams@meei.harvard.edu
Massachusetts Eye and Ear Infirmary · US

Funding

COCHLEAR HOMEOSTASISR01DC003929 · NIDCD · MASSACHUSETTS EYE AND EAR INFIRMARY · PI ADAMS, JOE C · 1999 to 2009
$2.8M
NIDCD NIH HHS DC003929NIDCD NIH HHS R01 DC003929
6 · The paper itself

Abstract

One of the more consistent and least understood changes in the aging human cochlea is the progressive loss of fibrocytes within the spiral ligament. This report presents an animal model for type IV fibrocyte loss, along with immunocytochemical evidence that noise-induced loss of these cells may account for previously unexplained hearing losses. The remarkably low threshold for noise-induced loss of type IV fibrocytes, approximately 24 dB less than the threshold for adjacent hair cell destruction, may account for the prevalence of missing fibrocytes in humans. In mice, changes in the spectrum of traumatizing noise had little effect upon the site of loss of the fibrocytes, suggesting that the primary site of damage that induced the loss was the basal-most cochlear turn, a site expected to be damaged by all three noise bands. Type IV fibrocytes were found to immunostain for connective tissue growth factor (CTGF) and for transforming growth factor beta receptor 3, a receptor that is known to activate CTGF expression. Type IV fibrocytes lack immunostaining for adenosine triphosphatase and connexins that are key players in potassium ion uptake and transmission, which suggests that they play little, if any, role in potassium recycling from perilymphatic space to the endolymphatic space. Consequently, their loss probably does not directly reduce this process. Immunostaining for a receptor for CTGF, low-density-lipoprotein-related protein 1, indicated that CTGF acts as an autocrine and a paracrine agent within the cochlea. The lack of CTGF paracrine effects following noise-induced loss of type IV fibrocytes may account for previously unexplained hearing losses.

Indexed as

Adenosine TriphosphatasesAnimalsCell DeathCochleaConnective Tissue CellsConnective Tissue Growth FactorConnexinsDisease ProgressionHearing Loss, Noise-InducedMaleMiceMice, Inbred CBANoiseProteoglycansReceptors, Transforming Growth Factor betaSodium-Potassium-Chloride SymportersAdenosine TriphosphatasesbetaglycanCCN2 protein, mouseConnective Tissue Growth FactorConnexinsProteoglycansReceptors, Transforming Growth Factor betaSLC12A2 protein, humanSlc12a2 protein, mouseSodium-Potassium-Chloride SymportersSolute Carrier Family 12, Member 2

Identifiers

PMID19277783
PMCPMC3084383
OpenAlexW2037066837

What OpenQuestion holds

Textmetadata
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.