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Transcriptomic Signature of Leishmania Infected Mice Macrophages: A Metabolic Point of View

We analyzed the transcriptional signatures of mouse bone marrow-derived macrophages at different times after infection with promastigotes of the protozoan parasite Leishmania major. Ingenuity Pathway Analysis revealed that the macrophage metabolic pathways including carbohydrate and lipid metabolism...

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Autores principales: Rabhi, Imen, Rabhi, Sameh, Ben-Othman, Rym, Rasche, Axel, Daskalaki, Adriani, Trentin, Bernadette, Piquemal, David, Regnault, Béatrice, Descoteaux, Albert, Guizani-Tabbane, Lamia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3424254/
https://www.ncbi.nlm.nih.gov/pubmed/22928052
http://dx.doi.org/10.1371/journal.pntd.0001763
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author Rabhi, Imen
Rabhi, Sameh
Ben-Othman, Rym
Rasche, Axel
Daskalaki, Adriani
Trentin, Bernadette
Piquemal, David
Regnault, Béatrice
Descoteaux, Albert
Guizani-Tabbane, Lamia
author_facet Rabhi, Imen
Rabhi, Sameh
Ben-Othman, Rym
Rasche, Axel
Daskalaki, Adriani
Trentin, Bernadette
Piquemal, David
Regnault, Béatrice
Descoteaux, Albert
Guizani-Tabbane, Lamia
author_sort Rabhi, Imen
collection PubMed
description We analyzed the transcriptional signatures of mouse bone marrow-derived macrophages at different times after infection with promastigotes of the protozoan parasite Leishmania major. Ingenuity Pathway Analysis revealed that the macrophage metabolic pathways including carbohydrate and lipid metabolisms were among the most altered pathways at later time points of infection. Indeed, L. major promastiogtes induced increased mRNA levels of the glucose transporter and almost all of the genes associated with glycolysis and lactate dehydrogenase, suggesting a shift to anaerobic glycolysis. On the other hand, L. major promastigotes enhanced the expression of scavenger receptors involved in the uptake of Low-Density Lipoprotein (LDL), inhibited the expression of genes coding for proteins regulating cholesterol efflux, and induced the synthesis of triacylglycerides. These data suggested that Leishmania infection disturbs cholesterol and triglycerides homeostasis and may lead to cholesterol accumulation and foam cell formation. Using Filipin and Bodipy staining, we showed cholesterol and triglycerides accumulation in infected macrophages. Moreover, Bodipy-positive lipid droplets accumulated in close proximity to parasitophorous vacuoles, suggesting that intracellular L. major may take advantage of these organelles as high-energy substrate sources. While the effect of infection on cholesterol accumulation and lipid droplet formation was independent on parasite development, our data indicate that anaerobic glycolysis is actively induced by L. major during the establishment of infection.
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spelling pubmed-34242542012-08-27 Transcriptomic Signature of Leishmania Infected Mice Macrophages: A Metabolic Point of View Rabhi, Imen Rabhi, Sameh Ben-Othman, Rym Rasche, Axel Daskalaki, Adriani Trentin, Bernadette Piquemal, David Regnault, Béatrice Descoteaux, Albert Guizani-Tabbane, Lamia PLoS Negl Trop Dis Research Article We analyzed the transcriptional signatures of mouse bone marrow-derived macrophages at different times after infection with promastigotes of the protozoan parasite Leishmania major. Ingenuity Pathway Analysis revealed that the macrophage metabolic pathways including carbohydrate and lipid metabolisms were among the most altered pathways at later time points of infection. Indeed, L. major promastiogtes induced increased mRNA levels of the glucose transporter and almost all of the genes associated with glycolysis and lactate dehydrogenase, suggesting a shift to anaerobic glycolysis. On the other hand, L. major promastigotes enhanced the expression of scavenger receptors involved in the uptake of Low-Density Lipoprotein (LDL), inhibited the expression of genes coding for proteins regulating cholesterol efflux, and induced the synthesis of triacylglycerides. These data suggested that Leishmania infection disturbs cholesterol and triglycerides homeostasis and may lead to cholesterol accumulation and foam cell formation. Using Filipin and Bodipy staining, we showed cholesterol and triglycerides accumulation in infected macrophages. Moreover, Bodipy-positive lipid droplets accumulated in close proximity to parasitophorous vacuoles, suggesting that intracellular L. major may take advantage of these organelles as high-energy substrate sources. While the effect of infection on cholesterol accumulation and lipid droplet formation was independent on parasite development, our data indicate that anaerobic glycolysis is actively induced by L. major during the establishment of infection. Public Library of Science 2012-08-21 /pmc/articles/PMC3424254/ /pubmed/22928052 http://dx.doi.org/10.1371/journal.pntd.0001763 Text en © 2012 Rabhi et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Rabhi, Imen
Rabhi, Sameh
Ben-Othman, Rym
Rasche, Axel
Daskalaki, Adriani
Trentin, Bernadette
Piquemal, David
Regnault, Béatrice
Descoteaux, Albert
Guizani-Tabbane, Lamia
Transcriptomic Signature of Leishmania Infected Mice Macrophages: A Metabolic Point of View
title Transcriptomic Signature of Leishmania Infected Mice Macrophages: A Metabolic Point of View
title_full Transcriptomic Signature of Leishmania Infected Mice Macrophages: A Metabolic Point of View
title_fullStr Transcriptomic Signature of Leishmania Infected Mice Macrophages: A Metabolic Point of View
title_full_unstemmed Transcriptomic Signature of Leishmania Infected Mice Macrophages: A Metabolic Point of View
title_short Transcriptomic Signature of Leishmania Infected Mice Macrophages: A Metabolic Point of View
title_sort transcriptomic signature of leishmania infected mice macrophages: a metabolic point of view
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3424254/
https://www.ncbi.nlm.nih.gov/pubmed/22928052
http://dx.doi.org/10.1371/journal.pntd.0001763
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