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spelling paper:paper_15359778_v2_n4_p756_Salto2023-06-08T16:20:07Z Formation and remodeling of inositolphosphoceramide during differentiation of Trypanosoma cruzi from trypomastigote to amastigote aureobasidin A cyclopeptide depsipeptide enzyme inhibitor glycosphingolipid inositolphosphoceramides membrane lipid membrane protein phosphatidylinositol animal article cell culture cell differentiation cell membrane cell size Chagas disease drug effect electron microscopy metabolism parasitology pH physiology Trypanosoma cruzi ultrastructure Animals Cell Differentiation Cell Membrane Cell Size Cells, Cultured Chagas Disease Depsipeptides Enzyme Inhibitors Glycosphingolipids Hydrogen-Ion Concentration Membrane Glycoproteins Membrane Lipids Microscopy, Electron Peptides, Cyclic Phosphatidylinositols Trypanosoma cruzi Animalia Eukaryota Invertebrata Protozoa Trypanosoma Trypanosoma cruzi Differentiation of Trypanosoma cruzi trypomastigotes to amastigotes inside myoblasts or in vitro, at low extracellular pH, in the presence of [ 3H]palmitic acid or [3H]inositol revealed differential labeling of inositolphosphoceramide and phosphatidylinositol, suggesting that a remodeling process takes place in both lipids. Using 3H-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 A13, phospholipase A2, 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. 2003 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_15359778_v2_n4_p756_Salto http://hdl.handle.net/20.500.12110/paper_15359778_v2_n4_p756_Salto
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic aureobasidin A
cyclopeptide
depsipeptide
enzyme inhibitor
glycosphingolipid
inositolphosphoceramides
membrane lipid
membrane protein
phosphatidylinositol
animal
article
cell culture
cell differentiation
cell membrane
cell size
Chagas disease
drug effect
electron microscopy
metabolism
parasitology
pH
physiology
Trypanosoma cruzi
ultrastructure
Animals
Cell Differentiation
Cell Membrane
Cell Size
Cells, Cultured
Chagas Disease
Depsipeptides
Enzyme Inhibitors
Glycosphingolipids
Hydrogen-Ion Concentration
Membrane Glycoproteins
Membrane Lipids
Microscopy, Electron
Peptides, Cyclic
Phosphatidylinositols
Trypanosoma cruzi
Animalia
Eukaryota
Invertebrata
Protozoa
Trypanosoma
Trypanosoma cruzi
spellingShingle aureobasidin A
cyclopeptide
depsipeptide
enzyme inhibitor
glycosphingolipid
inositolphosphoceramides
membrane lipid
membrane protein
phosphatidylinositol
animal
article
cell culture
cell differentiation
cell membrane
cell size
Chagas disease
drug effect
electron microscopy
metabolism
parasitology
pH
physiology
Trypanosoma cruzi
ultrastructure
Animals
Cell Differentiation
Cell Membrane
Cell Size
Cells, Cultured
Chagas Disease
Depsipeptides
Enzyme Inhibitors
Glycosphingolipids
Hydrogen-Ion Concentration
Membrane Glycoproteins
Membrane Lipids
Microscopy, Electron
Peptides, Cyclic
Phosphatidylinositols
Trypanosoma cruzi
Animalia
Eukaryota
Invertebrata
Protozoa
Trypanosoma
Trypanosoma cruzi
Formation and remodeling of inositolphosphoceramide during differentiation of Trypanosoma cruzi from trypomastigote to amastigote
topic_facet aureobasidin A
cyclopeptide
depsipeptide
enzyme inhibitor
glycosphingolipid
inositolphosphoceramides
membrane lipid
membrane protein
phosphatidylinositol
animal
article
cell culture
cell differentiation
cell membrane
cell size
Chagas disease
drug effect
electron microscopy
metabolism
parasitology
pH
physiology
Trypanosoma cruzi
ultrastructure
Animals
Cell Differentiation
Cell Membrane
Cell Size
Cells, Cultured
Chagas Disease
Depsipeptides
Enzyme Inhibitors
Glycosphingolipids
Hydrogen-Ion Concentration
Membrane Glycoproteins
Membrane Lipids
Microscopy, Electron
Peptides, Cyclic
Phosphatidylinositols
Trypanosoma cruzi
Animalia
Eukaryota
Invertebrata
Protozoa
Trypanosoma
Trypanosoma cruzi
description Differentiation of Trypanosoma cruzi trypomastigotes to amastigotes inside myoblasts or in vitro, at low extracellular pH, in the presence of [ 3H]palmitic acid or [3H]inositol revealed differential labeling of inositolphosphoceramide and phosphatidylinositol, suggesting that a remodeling process takes place in both lipids. Using 3H-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 A13, phospholipase A2, 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.
title Formation and remodeling of inositolphosphoceramide during differentiation of Trypanosoma cruzi from trypomastigote to amastigote
title_short Formation and remodeling of inositolphosphoceramide during differentiation of Trypanosoma cruzi from trypomastigote to amastigote
title_full Formation and remodeling of inositolphosphoceramide during differentiation of Trypanosoma cruzi from trypomastigote to amastigote
title_fullStr Formation and remodeling of inositolphosphoceramide during differentiation of Trypanosoma cruzi from trypomastigote to amastigote
title_full_unstemmed Formation and remodeling of inositolphosphoceramide during differentiation of Trypanosoma cruzi from trypomastigote to amastigote
title_sort formation and remodeling of inositolphosphoceramide during differentiation of trypanosoma cruzi from trypomastigote to amastigote
publishDate 2003
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_15359778_v2_n4_p756_Salto
http://hdl.handle.net/20.500.12110/paper_15359778_v2_n4_p756_Salto
_version_ 1768544056123588608