TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi

Autores
Sternlieb, Tamara; Schoijet, Alejandra Cecilia; Genta, Patricio; Alonso, Guillermo Daniel
Año de publicación
2020
Idioma
inglés
Tipo de recurso
documento de conferencia
Estado
versión publicada
Descripción
The AMP-activated protein kinase (AMPK) is a heterotrimeric enzyme involved in maintaining energy homeostasis in response to different stresses in many organisms. During the transition between the mammalian host and the insect vector, Trypanosoma cruzi, the causative agent of Chagas disease, faces different types of environmental fluctuations, all of which prompt the parasite to remodel its metabolism to adapt, survive and differentiate into the next stages of its life cycle. Recently, it was shown that Trypanosoma brucei AMPK is involved in the differentiation from the bloodstream slender to stumpy stage and in surface protein expression changes in response to nutritional stress. This underscores the relevance of AMPK for parasite life cycle progression. We identified four genes for the AMPK subunits of T. cruzi (α1 and α2 catalytic subunits, β and γ regulatory subunits). The β and γ subunits are largely conserved in their domain structure relative to the mammalian orthologs. However, the alpha subunits show significant sequence, structure and evolutionary differences from the human counterparts. The presence of these subunits in epimastigotes was confirmed by several techniques. TcAMPKα1 over-expressing epimastigotes showed a lower growth rate in basal culture conditions compared to the control, while α2 over-expression had the opposite effect. We found there is upregulation of AMPK activity under starvation, which is prevented if glucose is present in the culture medium. Each of these subunits could complement the ?glucose dependent? phenotype of S. cerevisiae conditional mutants lacking the respective subunit of the AMPK ortholog SNF1. Starvation and Monodansylcadaverine incorporation assays with AMPKα over-expressing parasites also showed a possible role of AMPK in autophagy. Finally, we explore the pathways in which TcAMPK may be involved using in silico analysis of putative substrates. Our results open the door to the study of the AMPK signaling pathway in Trypanosoma cruzi.
Fil: Sternlieb, Tamara. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Schoijet, Alejandra Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Genta, Patricio. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Alonso, Guillermo Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
XXXII Reunión Anual de la Sociedad Argentina de Protozoología
Ciudad Autónoma de Buenos Aires
Argentina
Sociedad Argentina de Protozoología
Materia
TRYPANOSOMA CRUZI
AMPK
ENERGY HOMEOSTASIS
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/201599

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spelling TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruziSternlieb, TamaraSchoijet, Alejandra CeciliaGenta, PatricioAlonso, Guillermo DanielTRYPANOSOMA CRUZIAMPKENERGY HOMEOSTASIShttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1The AMP-activated protein kinase (AMPK) is a heterotrimeric enzyme involved in maintaining energy homeostasis in response to different stresses in many organisms. During the transition between the mammalian host and the insect vector, Trypanosoma cruzi, the causative agent of Chagas disease, faces different types of environmental fluctuations, all of which prompt the parasite to remodel its metabolism to adapt, survive and differentiate into the next stages of its life cycle. Recently, it was shown that Trypanosoma brucei AMPK is involved in the differentiation from the bloodstream slender to stumpy stage and in surface protein expression changes in response to nutritional stress. This underscores the relevance of AMPK for parasite life cycle progression. We identified four genes for the AMPK subunits of T. cruzi (α1 and α2 catalytic subunits, β and γ regulatory subunits). The β and γ subunits are largely conserved in their domain structure relative to the mammalian orthologs. However, the alpha subunits show significant sequence, structure and evolutionary differences from the human counterparts. The presence of these subunits in epimastigotes was confirmed by several techniques. TcAMPKα1 over-expressing epimastigotes showed a lower growth rate in basal culture conditions compared to the control, while α2 over-expression had the opposite effect. We found there is upregulation of AMPK activity under starvation, which is prevented if glucose is present in the culture medium. Each of these subunits could complement the ?glucose dependent? phenotype of S. cerevisiae conditional mutants lacking the respective subunit of the AMPK ortholog SNF1. Starvation and Monodansylcadaverine incorporation assays with AMPKα over-expressing parasites also showed a possible role of AMPK in autophagy. Finally, we explore the pathways in which TcAMPK may be involved using in silico analysis of putative substrates. Our results open the door to the study of the AMPK signaling pathway in Trypanosoma cruzi.Fil: Sternlieb, Tamara. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Schoijet, Alejandra Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Genta, Patricio. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Alonso, Guillermo Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaXXXII Reunión Anual de la Sociedad Argentina de ProtozoologíaCiudad Autónoma de Buenos AiresArgentinaSociedad Argentina de ProtozoologíaSociedad Argentina de ProtozoologíaRiarte, Adelina RosaLonghi, Silvia AndreaFrank, Fernanda María2020info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectReuniónBookhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/201599TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi; XXXII Reunión Anual de la Sociedad Argentina de Protozoología; Ciudad Autónoma de Buenos Aires; Argentina; 2020; 56-56CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://protozoologia.org.ar/wp-content/uploads/Libro-de-Resumenes-SAP-2020.pdfInternacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:47:34Zoai:ri.conicet.gov.ar:11336/201599instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:47:34.631CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi
title TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi
spellingShingle TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi
Sternlieb, Tamara
TRYPANOSOMA CRUZI
AMPK
ENERGY HOMEOSTASIS
title_short TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi
title_full TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi
title_fullStr TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi
title_full_unstemmed TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi
title_sort TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi
dc.creator.none.fl_str_mv Sternlieb, Tamara
Schoijet, Alejandra Cecilia
Genta, Patricio
Alonso, Guillermo Daniel
author Sternlieb, Tamara
author_facet Sternlieb, Tamara
Schoijet, Alejandra Cecilia
Genta, Patricio
Alonso, Guillermo Daniel
author_role author
author2 Schoijet, Alejandra Cecilia
Genta, Patricio
Alonso, Guillermo Daniel
author2_role author
author
author
dc.contributor.none.fl_str_mv Riarte, Adelina Rosa
Longhi, Silvia Andrea
Frank, Fernanda María
dc.subject.none.fl_str_mv TRYPANOSOMA CRUZI
AMPK
ENERGY HOMEOSTASIS
topic TRYPANOSOMA CRUZI
AMPK
ENERGY HOMEOSTASIS
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The AMP-activated protein kinase (AMPK) is a heterotrimeric enzyme involved in maintaining energy homeostasis in response to different stresses in many organisms. During the transition between the mammalian host and the insect vector, Trypanosoma cruzi, the causative agent of Chagas disease, faces different types of environmental fluctuations, all of which prompt the parasite to remodel its metabolism to adapt, survive and differentiate into the next stages of its life cycle. Recently, it was shown that Trypanosoma brucei AMPK is involved in the differentiation from the bloodstream slender to stumpy stage and in surface protein expression changes in response to nutritional stress. This underscores the relevance of AMPK for parasite life cycle progression. We identified four genes for the AMPK subunits of T. cruzi (α1 and α2 catalytic subunits, β and γ regulatory subunits). The β and γ subunits are largely conserved in their domain structure relative to the mammalian orthologs. However, the alpha subunits show significant sequence, structure and evolutionary differences from the human counterparts. The presence of these subunits in epimastigotes was confirmed by several techniques. TcAMPKα1 over-expressing epimastigotes showed a lower growth rate in basal culture conditions compared to the control, while α2 over-expression had the opposite effect. We found there is upregulation of AMPK activity under starvation, which is prevented if glucose is present in the culture medium. Each of these subunits could complement the ?glucose dependent? phenotype of S. cerevisiae conditional mutants lacking the respective subunit of the AMPK ortholog SNF1. Starvation and Monodansylcadaverine incorporation assays with AMPKα over-expressing parasites also showed a possible role of AMPK in autophagy. Finally, we explore the pathways in which TcAMPK may be involved using in silico analysis of putative substrates. Our results open the door to the study of the AMPK signaling pathway in Trypanosoma cruzi.
Fil: Sternlieb, Tamara. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Schoijet, Alejandra Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Genta, Patricio. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Alonso, Guillermo Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
XXXII Reunión Anual de la Sociedad Argentina de Protozoología
Ciudad Autónoma de Buenos Aires
Argentina
Sociedad Argentina de Protozoología
description The AMP-activated protein kinase (AMPK) is a heterotrimeric enzyme involved in maintaining energy homeostasis in response to different stresses in many organisms. During the transition between the mammalian host and the insect vector, Trypanosoma cruzi, the causative agent of Chagas disease, faces different types of environmental fluctuations, all of which prompt the parasite to remodel its metabolism to adapt, survive and differentiate into the next stages of its life cycle. Recently, it was shown that Trypanosoma brucei AMPK is involved in the differentiation from the bloodstream slender to stumpy stage and in surface protein expression changes in response to nutritional stress. This underscores the relevance of AMPK for parasite life cycle progression. We identified four genes for the AMPK subunits of T. cruzi (α1 and α2 catalytic subunits, β and γ regulatory subunits). The β and γ subunits are largely conserved in their domain structure relative to the mammalian orthologs. However, the alpha subunits show significant sequence, structure and evolutionary differences from the human counterparts. The presence of these subunits in epimastigotes was confirmed by several techniques. TcAMPKα1 over-expressing epimastigotes showed a lower growth rate in basal culture conditions compared to the control, while α2 over-expression had the opposite effect. We found there is upregulation of AMPK activity under starvation, which is prevented if glucose is present in the culture medium. Each of these subunits could complement the ?glucose dependent? phenotype of S. cerevisiae conditional mutants lacking the respective subunit of the AMPK ortholog SNF1. Starvation and Monodansylcadaverine incorporation assays with AMPKα over-expressing parasites also showed a possible role of AMPK in autophagy. Finally, we explore the pathways in which TcAMPK may be involved using in silico analysis of putative substrates. Our results open the door to the study of the AMPK signaling pathway in Trypanosoma cruzi.
publishDate 2020
dc.date.none.fl_str_mv 2020
dc.type.none.fl_str_mv info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/conferenceObject
Reunión
Book
http://purl.org/coar/resource_type/c_5794
info:ar-repo/semantics/documentoDeConferencia
status_str publishedVersion
format conferenceObject
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/201599
TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi; XXXII Reunión Anual de la Sociedad Argentina de Protozoología; Ciudad Autónoma de Buenos Aires; Argentina; 2020; 56-56
CONICET Digital
CONICET
url http://hdl.handle.net/11336/201599
identifier_str_mv TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi; XXXII Reunión Anual de la Sociedad Argentina de Protozoología; Ciudad Autónoma de Buenos Aires; Argentina; 2020; 56-56
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://protozoologia.org.ar/wp-content/uploads/Libro-de-Resumenes-SAP-2020.pdf
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
dc.coverage.none.fl_str_mv Internacional
dc.publisher.none.fl_str_mv Sociedad Argentina de Protozoología
publisher.none.fl_str_mv Sociedad Argentina de Protozoología
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
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repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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