Evidence map›Paper›PMID 19730443›Full record

ArticleCell death and differentiation2010

Features of programmed cell death in intact Xenopus oocytes and early embryos revealed by near-infrared fluorescence and real-time monitoring.

C E Johnson, C D Freel, S Kornbluth

Open access · greenAbstract read
In one paragraph

Article in Cell death and differentiation, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. TheBiomolecules · 2025
    Review
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  5. Emerin induces nuclear breakage inMolecular biology of the cell · 2018
    Article
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  10. Quality improvement in gastroenterology clinical practice.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2012
    Review
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  12. Article
  13. Article
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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

3 authors at 2 institutions in 1 country.

C E JohnsonDepartment of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27710, USA.
C D Freel
S Kornbluth
Duke University Hospital · USDuke Medical Center · US

Funding

Inhibition of Cytochrome c-induced Caspase ActivationR01CA102707 · NCI · DUKE UNIVERSITY · PI KORNBLUTH, SALLY A · 2003 to 2014
$2.6M
Control of caspase activation in apoptosisR01GM080333 · NIGMS · DUKE UNIVERSITY · PI KORNBLUTH, SALLY A · 2007 to 2015
$2.6M
NCI NIH HHS CA102707NCI NIH HHS R01 CA102707NIGMS NIH HHS R01 GM08033NIGMS NIH HHS R01 GM080333
6 · The paper itself

Abstract

Factors influencing apoptosis of vertebrate eggs and early embryos have been studied in cell-free systems and in intact embryos by analyzing individual apoptotic regulators or caspase activation in static samples. A novel method for monitoring caspase activity in living Xenopus oocytes and early embryos is described here. The approach, using microinjection of a near-infrared caspase substrate that emits fluorescence only after its proteolytic cleavage by active effector caspases, has enabled the elucidation of otherwise cryptic aspects of apoptotic regulation. In particular, we show that brief caspase activity (10 min) is sufficient to cause apoptotic death in this system. We illustrate a cytochrome c dose threshold in the oocyte, which is lowered by Smac, a protein that binds thereby neutralizing the inhibitor of apoptosis proteins. We show that meiotic oocytes develop resistance to cytochrome c, and that the eventual death of oocytes arrested in meiosis is caspase-independent. Finally, data acquired through imaging caspase activity in the Xenopus embryo suggest that apoptosis in very early development is not cell-autonomous. These studies both validate this assay as a useful tool for apoptosis research and reveal subtleties in the cell death program during early development. Moreover, this method offers a potentially valuable screening modality for identifying novel apoptotic regulators.

Indexed as

ApoptosisFluorescence Resonance Energy TransferAnimalsCaspases, EffectorCytochromes cEmbryo, NonmammalianFluorescent DyesIndolesInhibitor of Apoptosis ProteinsMicroinjectionsMitochondrial ProteinsOocytesSpectroscopy, Near-InfraredXenopus laevisXenopus ProteinsCaspases, EffectorCytochromes cDIABLO protein, XenopusFluorescent DyesIndolesInhibitor of Apoptosis ProteinsIRDye800Mitochondrial ProteinsXenopus Proteins

Identifiers

PMID19730443
PMCPMC2794955
OpenAlexW2126301092

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.