Evidence map›Paper›PMID 24316078›Full record

ArticleCell reports2013

TRPV3 channels mediate strontium-induced mouse-egg activation.

Ingrid Carvacho, Hoi Chang Lee, Rafael A Fissore, David E Clapham

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.3field-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

45 citing papers in PubMed, 73 citations in OpenAlex.

  1. Article
  2. Article
  3. The TRPV3 channel is a mediator of zinc influx and homeostasis in murine oocytes.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Review
  5. Review
  6. Article
  7. The signal that stimulates mammalian embryo development.Frontiers in cell and developmental biology · 2024
    Review
  8. Review
  9. ZneLife · 2023
    Article
  10. ZnbioRxiv : the preprint server for biology · 2023
    Article
  11. Essential role of MgCell reports · 2023
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Superovulation Does Not Alter Calcium Oscillations Following Fertilization.Frontiers in cell and developmental biology · 2021
    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

4 authors at 3 institutions in 1 country.

Ingrid CarvachoHoward Hughes Medical Institute, Department of Cardiology, Boston Children's Hospital, Boston, MA 02115, USA; Department of Neurobiology, Harvard Medical School, Boston, MA 02115, USA.
Hoi Chang LeeDepartment of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA 01003, USA.
Rafael A FissoreDepartment of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA 01003, USA.
David E ClaphamHoward Hughes Medical Institute, Department of Cardiology, Boston Children's Hospital, Boston, MA 02115, USA; Department of Neurobiology, Harvard Medical School, Boston, MA 02115, USA. Electronic address: dclapham@enders.tch.harvard.edu.
University of Massachusetts Amherst · USBoston Children's Hospital · USHarvard University · US

Funding

Male contraception/CatSper1,2 sperm-specific ion channelU01HD045857 · NICHD · CHILDREN'S HOSPITAL BOSTON · PI CLAPHAM, DAVID E. · 2004 to 2013
$2.2M
LP3R-1 Regulation and Egg ActivationR01HD051872 · NICHD · UNIVERSITY OF MASSACHUSETTS AMHERST · PI FISSORE, RAFAEL ANTONIO · 2007 to 2011
$1.3M
Howard Hughes Medical InstituteNICHD NIH HHS HD051872NICHD NIH HHS R01 HD051872NICHD NIH HHS U01 HD045857
6 · The paper itself

Abstract

In mammals, calcium influx is required for oocyte maturation and egg activation. The molecular identities of the calcium-permeant channels that underlie the initiation of embryonic development are not established. Here, we describe a transient receptor potential (TRP) ion channel current activated by TRP agonists that is absent in TrpV3(-/-) eggs. TRPV3 current is differentially expressed during oocyte maturation, reaching a peak of maximum density and activity at metaphase of meiosis II (MII), the stage of fertilization. Selective activation of TRPV3 channels provokes egg activation by mediating massive calcium entry. Widely used to activate eggs, strontium application is known to yield normal offspring in combination with somatic cell nuclear transfer. We show that TRPV3 is required for strontium influx, because TrpV3(-/-) eggs failed to conduct Sr(2+) or undergo strontium-induced activation. We propose that TRPV3 is a major mediator of calcium influx in mouse eggs and is a putative target for artificial egg activation.

Indexed as

ParthenogenesisAction PotentialsAnimalsCalcium SignalingFemaleGene DeletionIon TransportMeiosisMiceOocytesStrontiumTRPV Cation ChannelsStrontiumTrpv3 protein, mouseTRPV Cation Channels

Identifiers

PMID24316078
PMCPMC3918412
OpenAlexW2055405580

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.