Evidence map›Paper›PMID 24921927›Full record

ArticlePLoS neglected tropical diseases2014

Protein kinase C and extracellular signal-regulated kinase regulate movement, attachment, pairing and egg release in Schistosoma mansoni.

Margarida Ressurreição, Paulu De Saram, Ruth S Kirk, David Rollinson, Aidan M Emery, Nigel M Page, Angela J Davies, Anthony J Walker

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.6field-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

24 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
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  9. Effect of Praziquantel onPathogens (Basel, Switzerland) · 2020
    Article
  10. Article
  11. Frontiers in microbiology · 2020
    Article
  12. Targeting Kinases inFrontiers in veterinary science · 2020
    Article
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  14. Article
  15. Article
  16. 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

8 authors at 2 institutions in 1 country.

Margarida RessurreiçãoMolecular Parasitology Laboratory, School of Life Sciences, Kingston University, Kingston upon Thames, Surrey, United Kingdom; Wolfson Wellcome Biomedical Laboratories, Life Sciences Department, Natural History Museum, London, United Kingdom.
Paulu De SaramMolecular Parasitology Laboratory, School of Life Sciences, Kingston University, Kingston upon Thames, Surrey, United Kingdom; Wolfson Wellcome Biomedical Laboratories, Life Sciences Department, Natural History Museum, London, United Kingdom.
Ruth S KirkMolecular Parasitology Laboratory, School of Life Sciences, Kingston University, Kingston upon Thames, Surrey, United Kingdom.
David RollinsonWolfson Wellcome Biomedical Laboratories, Life Sciences Department, Natural History Museum, London, United Kingdom.
Aidan M EmeryWolfson Wellcome Biomedical Laboratories, Life Sciences Department, Natural History Museum, London, United Kingdom.
Nigel M PageMolecular Parasitology Laboratory, School of Life Sciences, Kingston University, Kingston upon Thames, Surrey, United Kingdom.
Angela J DaviesMolecular Parasitology Laboratory, School of Life Sciences, Kingston University, Kingston upon Thames, Surrey, United Kingdom.
Anthony J WalkerMolecular Parasitology Laboratory, School of Life Sciences, Kingston University, Kingston upon Thames, Surrey, United Kingdom.
Kingston University · GBNatural History Museum · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein kinases C (PKCs) and extracellular signal-regulated kinases (ERKs) are evolutionary conserved cell signalling enzymes that coordinate cell function. Here we have employed biochemical approaches using 'smart' antibodies and functional screening to unravel the importance of these enzymes to Schistosoma mansoni physiology. Various PKC and ERK isotypes were detected, and were differentially phosphorylated (activated) throughout the various S. mansoni life stages, suggesting isotype-specific roles and differences in signalling complexity during parasite development. Functional kinase mapping in adult worms revealed that activated PKC and ERK were particularly associated with the adult male tegument, musculature and oesophagus and occasionally with the oesophageal gland; other structures possessing detectable activated PKC and/or ERK included the Mehlis' gland, ootype, lumen of the vitellaria, seminal receptacle and excretory ducts. Pharmacological modulation of PKC and ERK activity in adult worms using GF109203X, U0126, or PMA, resulted in significant physiological disturbance commensurate with these proteins occupying a central position in signalling pathways associated with schistosome muscular activity, neuromuscular coordination, reproductive function, attachment and pairing. Increased activation of ERK and PKC was also detected in worms following praziquantel treatment, with increased signalling associated with the tegument and excretory system and activated ERK localizing to previously unseen structures, including the cephalic ganglia. These findings support roles for PKC and ERK in S. mansoni homeostasis, and identify these kinase groups as potential targets for chemotherapeutic treatments against human schistosomiasis, a neglected tropical disease of enormous public health significance.

Indexed as

Signal TransductionAnimalsAnimal StructuresAnthelminticsExtracellular Signal-Regulated MAP KinasesFemaleLocomotionMalePraziquantelProtein Kinase CProtein Kinase InhibitorsReproductionSchistosoma mansoniZygoteAnthelminticsExtracellular Signal-Regulated MAP KinasesPraziquantelProtein Kinase CProtein Kinase Inhibitors

Identifiers

PMID24921927
PMCPMC4055629
OpenAlexW2108084972

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.