Evidence map›Paper›PMID 25044230›Full record

ArticleThe Journal of comparative neurology2015

Adult c-Kit(+) progenitor cells are necessary for maintenance and regeneration of olfactory neurons.

Bradley J Goldstein, Garrett M Goss, Konstantinos E Hatzistergos, Erika B Rangel, Barbara Seidler, Dieter Saur, Joshua M Hare

Open access · greenAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

40 citing papers in PubMed, 49 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Strategies to Develop Regenerative Medicine Approaches for Olfactory Disorders.Clinical and experimental otorhinolaryngology · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. International consensus statement on allergy and rhinology: Olfaction.International forum of allergy & rhinology · 2022
    Review
  10. Novel Therapies in Olfactory Disorders.Current otorhinolaryngology reports · 2022
    Review
  11. Review
  12. A role for Sfrp2 in cardiomyogenesis in vivo.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  13. On the in vivo origin of human nasal mesenchymal stem cell cultures.Laryngoscope investigative otolaryngology · 2020
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  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

7 authors at 3 institutions in 3 countries.

Bradley J GoldsteinInterdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, Florida, 33136; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, Florida, 33136.
Garrett M Goss
Konstantinos E Hatzistergos
Erika B Rangel
Barbara Seidler
Dieter Saur
Joshua M Hare
University of Miami · USStem Cell Institute · PATechnical University of Munich · DE

Funding

Stem Cells for Dilated CardiomyopathyR01HL110737 · NHLBI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI HARE, JOSHUA M · 2011 to 2015
$3.2M
Nasal progenitor cells and olfactory neurogenesisK08DC013556 · NIDCD · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI GOLDSTEIN, BRADLEY J · 2014 to 2018
$1.1M
NHLBI NIH HHS R01 HL110737NHLBI NIH HHS R01HL110737-01NIDCD NIH HHS K08 DC013556NIDCD NIH HHS K08DC013556
6 · The paper itself

Abstract

The olfactory epithelium houses chemosensory neurons, which transmit odor information from the nose to the brain. In adult mammals, the olfactory epithelium is a uniquely robust neuroproliferative zone, with the ability to replenish its neuronal and non-neuronal populations due to the presence of germinal basal cells. The stem and progenitor cells of these germinal layers, and their regulatory mechanisms, remain incompletely defined. Here we show that progenitor cells expressing c-Kit, a receptor tyrosine kinase marking stem cells in a variety of embryonic tissues, are required for maintenance of the adult neuroepithelium. Mouse genetic fate-mapping analyses show that embryonically, a c-Kit(+) population contributes to olfactory neurogenesis. In adults under conditions of normal turnover, there is relatively sparse c-Kit(+) progenitor cell (ckPC) activity. However, after experimentally induced neuroepithelial injury, ckPCs are activated such that they reconstitute the neuronal population. There are also occasional non-neuronal cells found to arise from ckPCs. Moreover, the selective depletion of the ckPC population, utilizing temporally controlled targeted diphtheria toxin A expression, results in failure of neurogenesis after experimental injury. Analysis of this model indicates that most ckPCs reside among the globose basal cell populations and act downstream of horizontal basal cells, which can serve as stem cells. Identification of the requirement for olfactory c-Kit-expressing progenitors in olfactory maintenance provides new insight into the mechanisms involved in adult olfactory neurogenesis. Additionally, we define an important and previously unrecognized site of adult c-Kit activity.

Indexed as

AnimalsBlotting, WesternCell CountDermoscopyImmunohistochemistryMice, 129 StrainMice, Inbred C57BLMice, TransgenicMicroscopy, ConfocalNerve RegenerationNeural Stem CellsNeurogenesisOlfactory MucosaOlfactory Receptor NeuronsProto-Oncogene Proteins c-kitProto-Oncogene Proteins c-kitgrowth factorneurogenesisolfactory epitheliumreceptor tyrosine kinasestem cells

Identifiers

PMID25044230
PMCPMC4232589
OpenAlexW1675241412

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.