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Participation of Actin on Giardia lamblia Growth and Encystation
BACKGROUND: Microfilaments play a determinant role in different cell processes such as: motility, cell division, phagocytosis and intracellular transport; however, these structures are poorly understood in the parasite Giardia lamblia. METHODOLOGY AND PRINCIPAL FINDINGS: By confocal microscopy using...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2743995/ https://www.ncbi.nlm.nih.gov/pubmed/19774081 http://dx.doi.org/10.1371/journal.pone.0007156 |
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author | Castillo-Romero, Araceli Leon-Avila, Gloria Perez Rangel, Armando Cortes Zarate, Rafael Garcia Tovar, Carlos Hernandez, Jose Manuel |
author_facet | Castillo-Romero, Araceli Leon-Avila, Gloria Perez Rangel, Armando Cortes Zarate, Rafael Garcia Tovar, Carlos Hernandez, Jose Manuel |
author_sort | Castillo-Romero, Araceli |
collection | PubMed |
description | BACKGROUND: Microfilaments play a determinant role in different cell processes such as: motility, cell division, phagocytosis and intracellular transport; however, these structures are poorly understood in the parasite Giardia lamblia. METHODOLOGY AND PRINCIPAL FINDINGS: By confocal microscopy using TRITC-phalloidin, we found structured actin distributed in the entire trophozoite, the label stand out at the ventral disc, median body, flagella and around the nuclei. During Giardia encystation, a sequence of morphological changes concurrent to modifications on the distribution of structured actin and in the expression of actin mRNA were observed. To elucidate whether actin participates actively on growth and encystation, cells were treated with Cytochalasin D, Latrunculin A and Jasplakinolide and analyzed by confocal and scanning electron microscopy. All drugs caused a growth reduction (27 to 45%) and changes on the distribution of actin. Besides, 60 to 80% of trophozoites treated with the drugs, exhibited damage at the caudal region, alterations in the flagella and wrinkles-like on the plasma membrane. The drugs also altered the cyst-yield and the morphology, scanning electron microscopy revealed diminished cytokinesis, cysts with damages in the wall and alterations in the size and on the intermembranal space. Furthermore, the drugs caused a significant reduction of the intensity of flourescence-labeled CWP1 on ESV and on cyst wall, this was coincident with a reduction of CWP1 gene expression (34%). CONCLUSIONS AND SIGNIFICANCE: All our results, indicated an important role of actin in the morphology, growth and encystation and indirectly suggested an actin role in gene expression. |
format | Text |
id | pubmed-2743995 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-27439952009-09-23 Participation of Actin on Giardia lamblia Growth and Encystation Castillo-Romero, Araceli Leon-Avila, Gloria Perez Rangel, Armando Cortes Zarate, Rafael Garcia Tovar, Carlos Hernandez, Jose Manuel PLoS One Research Article BACKGROUND: Microfilaments play a determinant role in different cell processes such as: motility, cell division, phagocytosis and intracellular transport; however, these structures are poorly understood in the parasite Giardia lamblia. METHODOLOGY AND PRINCIPAL FINDINGS: By confocal microscopy using TRITC-phalloidin, we found structured actin distributed in the entire trophozoite, the label stand out at the ventral disc, median body, flagella and around the nuclei. During Giardia encystation, a sequence of morphological changes concurrent to modifications on the distribution of structured actin and in the expression of actin mRNA were observed. To elucidate whether actin participates actively on growth and encystation, cells were treated with Cytochalasin D, Latrunculin A and Jasplakinolide and analyzed by confocal and scanning electron microscopy. All drugs caused a growth reduction (27 to 45%) and changes on the distribution of actin. Besides, 60 to 80% of trophozoites treated with the drugs, exhibited damage at the caudal region, alterations in the flagella and wrinkles-like on the plasma membrane. The drugs also altered the cyst-yield and the morphology, scanning electron microscopy revealed diminished cytokinesis, cysts with damages in the wall and alterations in the size and on the intermembranal space. Furthermore, the drugs caused a significant reduction of the intensity of flourescence-labeled CWP1 on ESV and on cyst wall, this was coincident with a reduction of CWP1 gene expression (34%). CONCLUSIONS AND SIGNIFICANCE: All our results, indicated an important role of actin in the morphology, growth and encystation and indirectly suggested an actin role in gene expression. Public Library of Science 2009-09-23 /pmc/articles/PMC2743995/ /pubmed/19774081 http://dx.doi.org/10.1371/journal.pone.0007156 Text en Castillo-Romero 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 Castillo-Romero, Araceli Leon-Avila, Gloria Perez Rangel, Armando Cortes Zarate, Rafael Garcia Tovar, Carlos Hernandez, Jose Manuel Participation of Actin on Giardia lamblia Growth and Encystation |
title | Participation of Actin on Giardia lamblia Growth and Encystation |
title_full | Participation of Actin on Giardia lamblia Growth and Encystation |
title_fullStr | Participation of Actin on Giardia lamblia Growth and Encystation |
title_full_unstemmed | Participation of Actin on Giardia lamblia Growth and Encystation |
title_short | Participation of Actin on Giardia lamblia Growth and Encystation |
title_sort | participation of actin on giardia lamblia growth and encystation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2743995/ https://www.ncbi.nlm.nih.gov/pubmed/19774081 http://dx.doi.org/10.1371/journal.pone.0007156 |
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