A Trypanosoma cruzi phosphatidylinositol 3-kinase (TcVps34) is involved in osmoregulation and receptor-mediated endocytosis

Trypanosoma cruzi, the etiological agent of Chagas disease, has the ability to respond to a variety of environmental changes during its life cycle both in the insect vector and in the vertebrate host. Because regulation of transcription initiation seems to be nonfunctional in this parasite, it is im...

Descripción completa

Guardado en:
Detalles Bibliográficos
Publicado: 2008
Materias:
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00219258_v283_n46_p31541_Schoijet
http://hdl.handle.net/20.500.12110/paper_00219258_v283_n46_p31541_Schoijet
Aporte de:
id paper:paper_00219258_v283_n46_p31541_Schoijet
record_format dspace
spelling paper:paper_00219258_v283_n46_p31541_Schoijet2025-07-30T17:25:50Z A Trypanosoma cruzi phosphatidylinositol 3-kinase (TcVps34) is involved in osmoregulation and receptor-mediated endocytosis Cell membranes Chemical reactions Enzyme activity Enzyme inhibition Life cycle Phospholipids Phosphoric acid Signal transduction Chagas diseases Environmental changes Etiological agents Intracellular compartments Membrane trafficking Osmoregulation Overexpressing cells Overexpression Phosphatidylinositol Phosphoinositides Pyrophosphatase Regulation of transcriptions Regulatory mechanisms Regulatory volume decreases Signal transduction pathways Trypanosoma cruzi Vesicular trafficking Wild types Wortmannin Laws and legislation adenosine triphosphatase ly 294000 phosphatidylinositol 3 kinase phosphatidylinositol 3 kinase inhibitor unclassified drug wortmannin acidification article cell migration cell vacuole cell volume cellular distribution cellular stress response endocytosis enzyme assay enzyme inhibition enzyme specificity epimastigote gene overexpression nonhuman nucleotide sequence osmoregulation priority journal protein family protein function protein phosphorylation sequence analysis structural homology survival time tonoplast Trypanosoma cruzi wild type yeast 1-Phosphatidylinositol 3-Kinase Animals Cloning, Molecular Endocytosis Gene Expression Regulation, Enzymologic Inorganic Pyrophosphatase Microscopy, Electron, Scanning Microscopy, Electron, Transmission Molecular Sequence Data Phenotype Protein Kinase Inhibitors Proton-Translocating ATPases Saccharomyces cerevisiae Trypanosoma cruzi Water-Electrolyte Balance Hexapoda Trypanosoma cruzi Vertebrata Trypanosoma cruzi, the etiological agent of Chagas disease, has the ability to respond to a variety of environmental changes during its life cycle both in the insect vector and in the vertebrate host. Because regulation of transcription initiation seems to be nonfunctional in this parasite, it is important to investigate other regulatory mechanisms of adaptation. Regulatory mechanisms at the level of signal transduction pathways involving phosphoinositides are good candidates for this purpose. Here we report the identification of the first phosphatidylinositol 3-kinase (PI3K) in T. cruzi, with similarity with its yeast counterpart, Vps34p. TcVps34 specifically phosphorylates phosphatidylinositol to produce phosphatidylinositol 3-phosphate, thus confirming that it belongs to class III PI3K family. Overexpression of TcVps34 resulted in morphological and functional alterations related to vesicular trafficking. Although inhibition of TcVps34 with specific PI3K inhibitors, such as wortmannin and LY294,000, resulted in reduced regulatory volume decrease after hyposmotic stress, cells overexpressing this enzyme were resistant to these inhibitors. Furthermore, these cells were able to recover their original volume faster than wild type cells when they were submitted to severe hyposmotic stress. In addition, in TcVps34-overexpressing cells, the activities of vacuolar-H+-ATPase and vacuolar H+- pyrophosphatase were altered, suggesting defects in the acidification of intracellular compartments. Furthermore, receptor-mediated endocytosis was partially blocked although fluid phase endocytosis was not affected, confirming a function for TcVps34 in membrane trafficking. Taken together, these results strongly support that TcVps34 plays a prominent role in vital processes for T. cruzi survival such as osmoregulation, acidification, and vesicular trafficking. © 2008 by The American Society for Biochemistry and Molecular Biology, Inc. 2008 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00219258_v283_n46_p31541_Schoijet http://hdl.handle.net/20.500.12110/paper_00219258_v283_n46_p31541_Schoijet
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Cell membranes
Chemical reactions
Enzyme activity
Enzyme inhibition
Life cycle
Phospholipids
Phosphoric acid
Signal transduction
Chagas diseases
Environmental changes
Etiological agents
Intracellular compartments
Membrane trafficking
Osmoregulation
Overexpressing cells
Overexpression
Phosphatidylinositol
Phosphoinositides
Pyrophosphatase
Regulation of transcriptions
Regulatory mechanisms
Regulatory volume decreases
Signal transduction pathways
Trypanosoma cruzi
Vesicular trafficking
Wild types
Wortmannin
Laws and legislation
adenosine triphosphatase
ly 294000
phosphatidylinositol 3 kinase
phosphatidylinositol 3 kinase inhibitor
unclassified drug
wortmannin
acidification
article
cell migration
cell vacuole
cell volume
cellular distribution
cellular stress response
endocytosis
enzyme assay
enzyme inhibition
enzyme specificity
epimastigote
gene overexpression
nonhuman
nucleotide sequence
osmoregulation
priority journal
protein family
protein function
protein phosphorylation
sequence analysis
structural homology
survival time
tonoplast
Trypanosoma cruzi
wild type
yeast
1-Phosphatidylinositol 3-Kinase
Animals
Cloning, Molecular
Endocytosis
Gene Expression Regulation, Enzymologic
Inorganic Pyrophosphatase
Microscopy, Electron, Scanning
Microscopy, Electron, Transmission
Molecular Sequence Data
Phenotype
Protein Kinase Inhibitors
Proton-Translocating ATPases
Saccharomyces cerevisiae
Trypanosoma cruzi
Water-Electrolyte Balance
Hexapoda
Trypanosoma cruzi
Vertebrata
spellingShingle Cell membranes
Chemical reactions
Enzyme activity
Enzyme inhibition
Life cycle
Phospholipids
Phosphoric acid
Signal transduction
Chagas diseases
Environmental changes
Etiological agents
Intracellular compartments
Membrane trafficking
Osmoregulation
Overexpressing cells
Overexpression
Phosphatidylinositol
Phosphoinositides
Pyrophosphatase
Regulation of transcriptions
Regulatory mechanisms
Regulatory volume decreases
Signal transduction pathways
Trypanosoma cruzi
Vesicular trafficking
Wild types
Wortmannin
Laws and legislation
adenosine triphosphatase
ly 294000
phosphatidylinositol 3 kinase
phosphatidylinositol 3 kinase inhibitor
unclassified drug
wortmannin
acidification
article
cell migration
cell vacuole
cell volume
cellular distribution
cellular stress response
endocytosis
enzyme assay
enzyme inhibition
enzyme specificity
epimastigote
gene overexpression
nonhuman
nucleotide sequence
osmoregulation
priority journal
protein family
protein function
protein phosphorylation
sequence analysis
structural homology
survival time
tonoplast
Trypanosoma cruzi
wild type
yeast
1-Phosphatidylinositol 3-Kinase
Animals
Cloning, Molecular
Endocytosis
Gene Expression Regulation, Enzymologic
Inorganic Pyrophosphatase
Microscopy, Electron, Scanning
Microscopy, Electron, Transmission
Molecular Sequence Data
Phenotype
Protein Kinase Inhibitors
Proton-Translocating ATPases
Saccharomyces cerevisiae
Trypanosoma cruzi
Water-Electrolyte Balance
Hexapoda
Trypanosoma cruzi
Vertebrata
A Trypanosoma cruzi phosphatidylinositol 3-kinase (TcVps34) is involved in osmoregulation and receptor-mediated endocytosis
topic_facet Cell membranes
Chemical reactions
Enzyme activity
Enzyme inhibition
Life cycle
Phospholipids
Phosphoric acid
Signal transduction
Chagas diseases
Environmental changes
Etiological agents
Intracellular compartments
Membrane trafficking
Osmoregulation
Overexpressing cells
Overexpression
Phosphatidylinositol
Phosphoinositides
Pyrophosphatase
Regulation of transcriptions
Regulatory mechanisms
Regulatory volume decreases
Signal transduction pathways
Trypanosoma cruzi
Vesicular trafficking
Wild types
Wortmannin
Laws and legislation
adenosine triphosphatase
ly 294000
phosphatidylinositol 3 kinase
phosphatidylinositol 3 kinase inhibitor
unclassified drug
wortmannin
acidification
article
cell migration
cell vacuole
cell volume
cellular distribution
cellular stress response
endocytosis
enzyme assay
enzyme inhibition
enzyme specificity
epimastigote
gene overexpression
nonhuman
nucleotide sequence
osmoregulation
priority journal
protein family
protein function
protein phosphorylation
sequence analysis
structural homology
survival time
tonoplast
Trypanosoma cruzi
wild type
yeast
1-Phosphatidylinositol 3-Kinase
Animals
Cloning, Molecular
Endocytosis
Gene Expression Regulation, Enzymologic
Inorganic Pyrophosphatase
Microscopy, Electron, Scanning
Microscopy, Electron, Transmission
Molecular Sequence Data
Phenotype
Protein Kinase Inhibitors
Proton-Translocating ATPases
Saccharomyces cerevisiae
Trypanosoma cruzi
Water-Electrolyte Balance
Hexapoda
Trypanosoma cruzi
Vertebrata
description Trypanosoma cruzi, the etiological agent of Chagas disease, has the ability to respond to a variety of environmental changes during its life cycle both in the insect vector and in the vertebrate host. Because regulation of transcription initiation seems to be nonfunctional in this parasite, it is important to investigate other regulatory mechanisms of adaptation. Regulatory mechanisms at the level of signal transduction pathways involving phosphoinositides are good candidates for this purpose. Here we report the identification of the first phosphatidylinositol 3-kinase (PI3K) in T. cruzi, with similarity with its yeast counterpart, Vps34p. TcVps34 specifically phosphorylates phosphatidylinositol to produce phosphatidylinositol 3-phosphate, thus confirming that it belongs to class III PI3K family. Overexpression of TcVps34 resulted in morphological and functional alterations related to vesicular trafficking. Although inhibition of TcVps34 with specific PI3K inhibitors, such as wortmannin and LY294,000, resulted in reduced regulatory volume decrease after hyposmotic stress, cells overexpressing this enzyme were resistant to these inhibitors. Furthermore, these cells were able to recover their original volume faster than wild type cells when they were submitted to severe hyposmotic stress. In addition, in TcVps34-overexpressing cells, the activities of vacuolar-H+-ATPase and vacuolar H+- pyrophosphatase were altered, suggesting defects in the acidification of intracellular compartments. Furthermore, receptor-mediated endocytosis was partially blocked although fluid phase endocytosis was not affected, confirming a function for TcVps34 in membrane trafficking. Taken together, these results strongly support that TcVps34 plays a prominent role in vital processes for T. cruzi survival such as osmoregulation, acidification, and vesicular trafficking. © 2008 by The American Society for Biochemistry and Molecular Biology, Inc.
title A Trypanosoma cruzi phosphatidylinositol 3-kinase (TcVps34) is involved in osmoregulation and receptor-mediated endocytosis
title_short A Trypanosoma cruzi phosphatidylinositol 3-kinase (TcVps34) is involved in osmoregulation and receptor-mediated endocytosis
title_full A Trypanosoma cruzi phosphatidylinositol 3-kinase (TcVps34) is involved in osmoregulation and receptor-mediated endocytosis
title_fullStr A Trypanosoma cruzi phosphatidylinositol 3-kinase (TcVps34) is involved in osmoregulation and receptor-mediated endocytosis
title_full_unstemmed A Trypanosoma cruzi phosphatidylinositol 3-kinase (TcVps34) is involved in osmoregulation and receptor-mediated endocytosis
title_sort trypanosoma cruzi phosphatidylinositol 3-kinase (tcvps34) is involved in osmoregulation and receptor-mediated endocytosis
publishDate 2008
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00219258_v283_n46_p31541_Schoijet
http://hdl.handle.net/20.500.12110/paper_00219258_v283_n46_p31541_Schoijet
_version_ 1840321663555600384