Evidence map›Paper›PMID 24241124›Full record

ArticleParasitology research2014

Extracellular vesicles shed by Trypanosoma cruzi are linked to small RNA pathways, life cycle regulation, and susceptibility to infection of mammalian cells.

Maria R Garcia-Silva, Roberta Ferreira Cura das Neves, Florencia Cabrera-Cabrera, Julia Sanguinetti, Lia C Medeiros, Carlos Robello, Hugo Naya, Tamara Fernandez-Calero, Thais Souto-Padron, Wanderley de Souza and 1 more

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Article in Parasitology research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 104 papers.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

104 citing papers in PubMed, 156 citations in OpenAlex.

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  4. Proceedings of the National Academy of Sciences of the United States of America · 2025
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  12. Proceedings of the National Academy of Sciences of the United States of America · 2024
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  20. The Molecular Mechanisms Employed by the ParasiteInternational journal of molecular sciences · 2023
    Article

44 more citing papers are in PubMed but not listed here.

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

11 authors at 3 institutions in 2 countries.

Maria R Garcia-SilvaFunctional Genomics Unit, Institut Pasteur de Montevideo, Mataojo 2020, Montevideo, CP 11400, Uruguay.
Roberta Ferreira Cura das Neves
Florencia Cabrera-Cabrera
Julia Sanguinetti
Lia C Medeiros
Carlos Robello
Hugo Naya
Tamara Fernandez-Calero
Thais Souto-Padron
Wanderley de Souza
Alfonso Cayota
Institut Pasteur de Montevideo · UYUniversidade Federal do Rio de Janeiro · BRUniversidad de Montevideo · UY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The protozoan parasite Trypanosoma cruzi has a complex life cycle characterized by intracellular and extracellular forms alternating between invertebrate and mammals. To cope with these changing environments, T. cruzi undergoes rapid changes in gene expression, which are achieved essentially at the posttranscriptional level. At present, expanding families of small RNAs are recognized as key players in novel forms of posttranscriptional gene regulation in most eukaryotes. However, T. cruzi lacks canonical small RNA pathways. In a recent work, we reported the presence of alternate small RNA pathways in T. cruzi mainly represented by a homogeneous population of tRNA-derived small RNAs (tsRNAs). In T. cruzi epimastigotes submitted to nutrient starvation, tsRNAs colocalized with an argonaute protein distinctive of trypanosomatids (TcPIWI-tryp) and were recruited to particular cytoplasmic granules. Using epifluorescence and electronic microscopy, we observed that tsRNAs and the TcPIWI-tryp protein were recruited mainly to reservosomes and other intracellular vesicles including endosome-like vesicles and vesicular structures resembling the Golgi complex. These data suggested that, in T. cruzi, tsRNA biogenesis is probably part of endocytic/exocytic routes. We also demonstrated that epimastigotes submitted to nutrient starvation shed high levels of vesicles to the extracellular medium, which carry small tRNAs and TcPIWI-tryp proteins as cargo. At least a fraction of extracellular vesicle cargo was transferred between parasites and to mammalian susceptible cells. Our data afford experimental evidence, indicating that extracellular vesicles shed by T. cruzi promote not only life cycle transition of epimastigotes to trypomastigote forms but also infection susceptibility of mammalian cells.

Indexed as

AnimalsChlorocebus aethiopsCytoplasmic VesiclesEndosomesGolgi ApparatusHumansK562 CellsLife Cycle StagesMicroscopy, Electron, TransmissionRNA, ProtozoanRNA, TransferTrypanosoma cruziVero CellsRNA, ProtozoanRNA, Transfer

Identifiers

PMID24241124
OpenAlexW2005302773

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.