Evidence map›Paper›PMID 12912895›Full record

ArticleEukaryotic cell2003

Formation and remodeling of inositolphosphoceramide during differentiation of Trypanosoma cruzi from trypomastigote to amastigote.

Maria Laura Salto, Laura E Bertello, Mauricio Vieira, Roberto Docampo, Silvia N J Moreno, Rosa M de Lederkremer

Open access · diamondAbstract read
In one paragraph

Article in Eukaryotic cell, 2003. 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
2.4field-weighted citation impact, top 11% 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, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Phospholipid and sphingolipid metabolism in Leishmania.Molecular and biochemical parasitology · 2010
    Review
  13. Sphingolipids in parasitic protozoa.Advances in experimental medicine and biology · 2010
    Review
  14. Article
  15. Sterol Biosynthesis Pathway as Target for Anti-trypanosomatid Drugs.Interdisciplinary perspectives on infectious diseases · 2009
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Inhibitory effect of aureobasidin A on Toxoplasma gondii.Antimicrobial agents and chemotherapy · 2005
    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.

Maria Laura SaltoLaboratory of Molecular Parasitology, Department of Pathobiology and Center for Zoonoses Research, College of Veterinary Medicine, University of Illinois at Urbana-Champaign, 61802, USA.
Laura E Bertello
Mauricio Vieira
Roberto Docampo
Silvia N J Moreno
Rosa M de Lederkremer
University of Illinois Urbana-Champaign · USFundación Ciencias Exactas y Naturales · AR

Funding

The role of phospholipase C in Trypanosoma cruziR21AI048039 · NIAID · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI MORENO, SILVIA N · 2001 to 2001
$230k
NIAID NIH HHS AI-48039
6 · The paper itself

Abstract

Differentiation of Trypanosoma cruzi trypomastigotes to amastigotes inside myoblasts or in vitro, at low extracellular pH, in the presence of [(3)H]palmitic acid or [(3)H]inositol revealed differential labeling of inositolphosphoceramide and phosphatidylinositol, suggesting that a remodeling process takes place in both lipids. Using (3)H-labeled inositolphosphoceramide and phosphatidylinositol as substrates, we demonstrated the association of at least five enzymatic activities with the membranes of amastigotes and trypomastigotes. These included phospholipase A(1), phospholipase A(2), inositolphosphoceramide-fatty acid hydrolase, acyltransferase, and a phospholipase C releasing either ceramide or a glycerolipid from the inositolphospholipids. These enzymes may be acting in remodeling reactions leading to the anchor of mature glycoproteins or glycoinositolphospholipids and helping in the transformation of the plasma membrane, a necessary step in the differentiation of slender trypomastigotes to round amastigotes. Synthesis of inositolphosphoceramide and particularly of glycoinositolphospholipids was inhibited by aureobasidin A, a known inhibitor of fungal inositolphosphoceramide synthases. The antibiotic impaired the differentiation of trypomastigotes at acidic pH, as indicated by an increased appearance of intermediate forms and a decreased expression of the Ssp4 glycoprotein, a characteristic marker of amastigote forms. Aureobasidin A was also toxic to differentiating trypomastigotes at acidic pH but not to trypomastigotes maintained at neutral pH. Our data suggest that inositolphosphoceramide is implicated in T. cruzi differentiation and that its metabolism could provide important targets for the development of antiparasitic therapies.

Indexed as

DepsipeptidesAnimalsCell DifferentiationCell MembraneCells, CulturedCell SizeChagas DiseaseEnzyme InhibitorsGlycosphingolipidsHydrogen-Ion ConcentrationMembrane GlycoproteinsMembrane LipidsMicroscopy, ElectronPeptides, CyclicPhosphatidylinositolsTrypanosoma cruziaureobasidin ADepsipeptidesEnzyme InhibitorsGlycosphingolipidsinositolphosphoceramidesMembrane GlycoproteinsMembrane LipidsPeptides, CyclicPhosphatidylinositols

Identifiers

PMID12912895
PMCPMC178363
OpenAlexW2136311909

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.