Evidence map›Paper›PMID 16192635›Full record

ArticleThe American journal of pathology2005

Uptake of host cell transforming growth factor-beta by Trypanosoma cruzi amastigotes in cardiomyocytes: potential role in parasite cycle completion.

Mariana C Waghabi, Michelle Keramidas, Sabine Bailly, Wim Degrave, Leila Mendonça-Lima, Maria de Nazaré C Soeiro, Maria de Nazareth L Meirelles, Sidnei Paciornik, Tania C Araújo-Jorge, Jean-Jacques Feige

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

28 citing papers in PubMed, 51 citations in OpenAlex.

  1. Regulatory roles of PIWI-interacting RNAs in cardiovascular disease.American journal of physiology. Heart and circulatory physiology · 2025
    Review
  2. Article
  3. Review
  4. In Chagas disease, transforming growth factor beta neutralization reducesFrontiers in cellular and infection microbiology · 2022
    Article
  5. Mechanisms Associated withLife (Basel, Switzerland) · 2021
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. CD8Frontiers in cellular and infection microbiology · 2021
    Article
  11. Differential Role of TGF-β in Extracellular Matrix Regulation DuringInternational journal of molecular sciences · 2019
    Article
  12. Article
  13. Review
  14. Article
  15. TGF-Disease markers · 2018
    Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. 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

10 authors at 2 institutions in 2 countries.

Mariana C WaghabiLaboratorios de Biologia Celular, Instituto Oswaldo Cruz, Rio de Janeiro, Brazil.
Michelle Keramidas
Sabine Bailly
Wim Degrave
Leila Mendonça-Lima
Maria de Nazaré C Soeiro
Maria de Nazareth L Meirelles
Sidnei Paciornik
Tania C Araújo-Jorge
Jean-Jacques Feige
Fundação Oswaldo Cruz · BRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cytokine transforming growth factor-beta (TGF-beta) plays various functions in the control of Trypanosoma cruzi infectivity and in the progression of Chagas' disease. When we immunostained T. cruzi-infected cardiomyocytes (after either in vivo or in vitro infections) for TGF-beta, we observed stronger immunoreactivity in parasites than in host cells. TGF-beta immunoreactivity evolved during parasite cycle progression, with intense staining in amastigotes versus very faint staining in trypomastigotes. TGF-beta was present on the surface of amastigotes, in the flagellar pocket, and in intraparasitic vesicles as revealed by electron microscopy. However, no ortholog TGF-beta gene could be identified in the genome of T. cruzi by in silico analysis or by extensive polymerase chain reaction and reverse transcriptase-polymerase chain reaction studies. Immunoreactive TGF-beta was most probably taken up by the parasite from the host cell cytoplasm because such an internalization process of biotinylated TGF-beta could be observed in axenic amastigotes in vitro. These observations represent the first example of a novel mechanism by which a primitive unicellular protozoan can use host cell TGF-beta to control its own intracellular life cycle.

Indexed as

Life Cycle StagesActinsAnimalsCells, CulturedChagas DiseaseEmbryo, MammalianEmbryo, NonmammalianFluorescein-5-isothiocyanateFluorescent Antibody Technique, IndirectFluorescent DyesImmunohistochemistryIndolesMiceMicroscopy, ConfocalMyocytes, CardiacPhalloidineActinsDAPIFluorescein-5-isothiocyanateFluorescent DyesIndolesPhalloidineRecombinant ProteinsRhodaminesTransforming Growth Factor beta

Identifiers

PMID16192635
PMCPMC1603686
OpenAlexW13337459

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.