Evidence map›Paper›PMID 16572731›Full record

ArticleCell stress & chaperones2006

Inhibition of apoptosis by p26: implications for small heat shock protein function during Artemia development.

Tania S Villeneuve, Xiaocui Ma, Yu Sun, Mindy M Oulton, Ann E Oliver, Thomas H MacRae

Open access · greenAbstract read
In one paragraph

Article in Cell stress & chaperones, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 46 citations in OpenAlex.

  1. Crowding in Anhydrobiosis.Sub-cellular biochemistry · 2025
    Review
  2. Article
  3. Article
  4. Article
  5. Mechanisms of animal diapause: recent developments from nematodes, crustaceans, insects, and fish.American journal of physiology. Regulatory, integrative and comparative physiology · 2016
    Review
  6. Review
  7. Article
  8. Article
  9. Gene expression, metabolic regulation and stress tolerance during diapause.Cellular and molecular life sciences : CMLS · 2010
    Review
  10. Article
  11. 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

6 authors at 2 institutions in 2 countries.

Tania S VilleneuveDepartment of Biology, Dalhousie University, Halifax, NS B3H 4J1 Canada.
Xiaocui Ma
Yu Sun
Mindy M Oulton
Ann E Oliver
Thomas H MacRae
University of California, Davis · USDalhousie University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

p26, an abundantly expressed small heat shock protein, is thought to establish stress resistance in oviparously developing embryos of the crustacean Artemia franciscana by preventing irreversible protein denaturation, but it might also promote survival by inhibiting apoptosis. To test this possibility, stably transfected mammalian cells producing p26 were generated and their ability to resist apoptosis induction determined. Examination of immunofluorescently stained transfected 293H cells by confocal microscopy demonstrated p26 is diffusely distributed in the cytoplasm with a minor amount of the protein in nuclei. As shown by immunoprobing of Western blots, p26 constituted approximately 0.6% of soluble cell protein. p26 localization and quantity were unchanged during prolonged culture, and the protein had no apparent ill effects on transfected cells. Molecular sieve chromatography in Sepharose 6B revealed p26 oligomers of about 20 monomers, with a second fraction occurring as larger aggregates. A similar pattern was observed in sucrose gradients, but overall oligomer size was smaller. Mammalian cells containing p26 were more thermotolerant than cells transfected with the expression vector only, and as measured by annexin V labeling, Hoescht 33342 nuclear staining and procaspase-3 activation, transfected cells effectively resisted apoptosis induction by heat and staurosporine. The ability to confer thermotolerance and limit heat-induced apoptosis is important because Artemia embryos are frequently exposed to high temperature in their natural habitat. p26 also blocked apoptosis in transfected cells during drying and rehydration, findings with direct relevance to Artemia life history characteristics because desiccation terminates cyst diapause. Thus, in addition to functioning as a molecular chaperone, p26 inhibits apoptosis, an activity shared by other small heat shock proteins and with the potential to play an important role during Artemia embryo development.

Indexed as

ApoptosisAnimalsAnnexin A5ArtemiaBenzimidazolesBlotting, WesternCell LineDNA, ComplementaryEmbryo, NonmammalianEscherichia coliFluorescent Antibody Technique, IndirectFluorescent DyesHeat-Shock ProteinsHumansMicroscopy, ConfocalMolecular ChaperonesAnnexin A5Benzimidazolesbisbenzimide ethoxide trihydrochlorideDNA, ComplementaryFluorescent DyesHeat-Shock ProteinsMolecular Chaperonesp26 chaperone protein, Artemia franciscanaPiperazinesStaurosporinetriethylenediamine

Identifiers

PMID16572731
PMCPMC1400614
OpenAlexW2181214912

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.