Evidence map›Paper›PMID 26515404›Full record

ArticleScientific reports2015

Dental enamel cells express functional SOCE channels.

Meerim K Nurbaeva, Miriam Eckstein, Axel R Concepcion, Charles E Smith, Sonal Srikanth, Michael L Paine, Yousang Gwack, Michael J Hubbard, Stefan Feske, Rodrigo S Lacruz

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

35 citing papers in PubMed, 48 citations in OpenAlex.

  1. Developing Optogenetic Approaches to Study CaCold Spring Harbor perspectives in biology · 2026
    Review
  2. Article
  3. Mathematical Modeling of Calcium Dynamics in Ameloblasts.Calcified tissue international · 2026
    Article
  4. Mechanosensitive Piezo1 Channels in Enamel Cells.Calcified tissue international · 2026
    Article
  5. Article
  6. Review
  7. Roles of calcium in ameloblasts during tooth development: A scoping review.Journal of Taibah University Medical Sciences · 2025
    Review
  8. Article
  9. The circadian clock in enamel development.International journal of oral science · 2024
    Review
  10. Review
  11. Article
  12. Article
  13. Frontiers in physiology · 2023
    Article
  14. Article
  15. Article
  16. Mitochondria modulate ameloblast CaFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  17. Article
  18. Article
  19. 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

10 authors at 5 institutions in 3 countries.

Meerim K NurbaevaDept. Basic Science and Craniofacial Biology, New York University College of Dentistry, New York, NY 10010, USA.
Miriam EcksteinDept. Basic Science and Craniofacial Biology, New York University College of Dentistry, New York, NY 10010, USA.
Axel R ConcepcionDept. of Pathology, New York University School of Medicine, New York, NY 10016, USA.
Charles E SmithDepartment of Anatomy &Cell Biology, McGill University, Facility for Electron Microscopy Research, Montreal, H3A 2B2, Canada.
Sonal SrikanthDept. of Physiology, University of California, Los Angeles, 53-266 CHS, 10833 Le Conte Avenue, Los Angeles, California, USA.
Michael L PaineCenter for Craniofacial Molecular Biology, Ostrow School of Dentistry, University of Southern California, Los Angeles, California, CSA 135-HSC 9062, USA.
Yousang GwackDept. of Physiology, University of California, Los Angeles, 53-266 CHS, 10833 Le Conte Avenue, Los Angeles, California, USA.
Michael J HubbardDepartments of Paediatrics and Pharmacology, The University of Melbourne, Victoria 3010, Australia.
Stefan FeskeDept. of Pathology, New York University School of Medicine, New York, NY 10016, USA.
Rodrigo S LacruzDept. Basic Science and Craniofacial Biology, New York University College of Dentistry, New York, NY 10010, USA.
New York University · USUniversity of California, Los Angeles · USMcGill University · CAUniversity of Melbourne · AUUniversity of Southern California · US

Funding

CRAC Channel Deficiency in Immunity to InfectionR01AI097302 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI FESKE, STEFAN · 2012 to 2022
$5.6M
Novel regulators of store-operated Ca2+ entry in immune systemsR01AI083432 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GWACK, YOUSANG · 2009 to 2020
$3.8M
MOLECULAR MECHANISMS FOR EXTRACELLULAR PH CONTROL DURING AMELOGENESISR01DE019629 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI PAINE, MICHAEL LANSDELL · 2009 to 2014
$2.9M
Calcium Regulation and Oral HealthR00DE022799 · NIDCR · NEW YORK UNIVERSITY · PI LACRUZ, RODRIGO S. · 2014 to 2016
$728k
CALCIUM REGULATION IN ORAL HEALTHK99DE022799 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LACRUZ, RODRIGO S. · 2012 to 2013
$214k
Arthritis Research UKNIAID NIH HHS AI083432NIAID NIH HHS AI097302NIAID NIH HHS R01 AI083432NIAID NIH HHS R01 AI097302NIDCR NIH HHS DE019629NIDCR NIH HHS DE022799NIDCR NIH HHS K99 DE022799NIDCR NIH HHS R00 DE022799NIDCR NIH HHS R01 DE019629
6 · The paper itself

Abstract

Dental enamel formation requires large quantities of Ca(2+) yet the mechanisms mediating Ca(2+) dynamics in enamel cells are unclear. Store-operated Ca(2+) entry (SOCE) channels are important Ca(2+) influx mechanisms in many cells. SOCE involves release of Ca(2+) from intracellular pools followed by Ca(2+) entry. The best-characterized SOCE channels are the Ca(2+) release-activated Ca(2+) (CRAC) channels. As patients with mutations in the CRAC channel genes STIM1 and ORAI1 show abnormal enamel mineralization, we hypothesized that CRAC channels might be an important Ca(2+) uptake mechanism in enamel cells. Investigating primary murine enamel cells, we found that key components of CRAC channels (ORAI1, ORAI2, ORAI3, STIM1, STIM2) were expressed and most abundant during the maturation stage of enamel development. Furthermore, inositol 1,4,5-trisphosphate receptor (IP3R) but not ryanodine receptor (RyR) expression was high in enamel cells suggesting that IP3Rs are the main ER Ca(2+) release mechanism. Passive depletion of ER Ca(2+) stores with thapsigargin resulted in a significant raise in [Ca(2+)]i consistent with SOCE. In cells pre-treated with the CRAC channel blocker Synta-66 Ca(2+) entry was significantly inhibited. These data demonstrate that enamel cells have SOCE mediated by CRAC channels and implicate them as a mechanism for Ca(2+) uptake in enamel formation.

Indexed as

AmeloblastsAnimalsCalcium-Binding ProteinsCalcium Channel BlockersCalcium ChannelsCalcium SignalingCells, CulturedDental EnamelFura-2HumansInositol 1,4,5-Trisphosphate ReceptorsMaleMembrane GlycoproteinsMembrane ProteinsMiceMice, Inbred C57BLAtp2a2 protein, ratCalcium-Binding ProteinsCalcium Channel BlockersCalcium ChannelsFura-2Inositol 1,4,5-Trisphosphate ReceptorsMembrane GlycoproteinsMembrane ProteinsORAI1 ProteinOrai1 protein, ratRyanodine Receptor Calcium Release ChannelSarcoplasmic Reticulum Calcium-Transporting ATPasesStim1 protein, ratSTIM2 protein, ratStromal Interaction Molecule 1Stromal Interaction Molecule 2Thapsigargin

Identifiers

PMID26515404
PMCPMC4626795
OpenAlexW2415973705

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.