Evidence map›Paper›PMID 23250917›Full record

ArticleAnnals of botany2013

Mastoparan-induced programmed cell death in the unicellular alga Chlamydomonas reinhardtii.

Zhenya P Yordanova, Ernst J Woltering, Veneta M Kapchina-Toteva, Elena T Iakimova

Open access · bronzeAbstract read
In one paragraph

Article in Annals of botany, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.9field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 57 citations in OpenAlex.

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  6. A polyyne toxin produced by an antagonistic bacterium blinds and lyses a Chlamydomonad alga.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  7. Article
  8. Cell Death in Evolutionary Transitions in Individuality.The Yale journal of biology and medicine · 2019
    Review
  9. Review
  10. Article
  11. Active extracellular substances ofEngineering in life sciences · 2017
    Article
  12. Article
  13. 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 2 institutions in 2 countries.

Zhenya P YordanovaDepartment Plant Physiology, Sofia University 'St Kliment Ohridski', Sofia, Bulgaria.
Ernst J Woltering
Veneta M Kapchina-Toteva
Elena T Iakimova
Sofia University "St. Kliment Ohridski" · BGWageningen University & Research · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsUnder stress-promoting conditions unicellular algae can undergo programmed cell death (PCD) but the mechanisms of algal cellular suicide are still poorly understood. In this work, the involvement of caspase-like proteases, DNA cleavage and the morphological occurrence of cell death in wasp venom mastoparan (MP)-treated Chlamydomonas reinhardtii were studied.

methodsAlgal cells were exposed to MP and cell death was analysed over time. Specific caspase inhibitors were employed to elucidate the possible role of caspase-like proteases. YVADase activity (presumably a vacuolar processing enzyme) was assayed by using a fluorogenic caspase-1 substrate. DNA breakdown was evaluated by DNA laddering and Comet analysis. Cellular morphology was examined by confocal laser scanning microscopy. KEY

resultsMP-treated C. reinhardtii cells expressed several features of necrosis (protoplast shrinkage) and vacuolar cell death (lytic vesicles, vacuolization, empty cell-walled corpse-containing remains of digested protoplast) sometimes within one single cell and in different individual cells. Nucleus compaction and DNA fragmentation were detected. YVADase activity was rapidly stimulated in response to MP but the early cell death was not inhibited by caspase inhibitors. At later time points, however, the caspase inhibitors were effective in cell-death suppression. Conditioned medium from MP-treated cells offered protection against MP-induced cell death.

conclusionsIn C. reinhardtii MP triggered PCD of atypical phenotype comprising features of vacuolar and necrotic cell deaths, reminiscent of the modality of hypersensitive response. It was assumed that depending on the physiological state and sensitivity of the cells to MP, the early cell-death phase might be not mediated by caspase-like enzymes, whereas later cell death may involve caspase-like-dependent proteolysis. The findings substantiate the hypothesis that, depending on the mode of induction and sensitivity of the cells, algal PCD may take different forms and proceed through different pathways.

Indexed as

Algal ProteinsAnimalsCaspase InhibitorsCaspasesChlamydomonas reinhardtiiDNA Degradation, NecroticIntercellular Signaling Peptides and ProteinsNecrosisPeptidesPhenotypeSignal TransductionWaspsWasp VenomsAlgal ProteinsCaspase InhibitorsCaspasesIntercellular Signaling Peptides and ProteinsmastoparanPeptidesWasp Venoms

Identifiers

PMID23250917
PMCPMC3555528
OpenAlexW2147744658

What OpenQuestion holds

Textmetadata
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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.