Myosin II and the Gal-GalNAc lectin play a crucial role in tissue invasion by Entamoeba histolytica
Autor: | Coudrier, Evelyne, Amblard, François, Zimmer, Christophe, Roux, Pascal, Olivo-Marin, Jean-Christophe, Rigothier, Marie-Christine, Guillén, Nancy |
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Přispěvatelé: | Compartimentation et dynamique cellulaires (CDC), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut Curie [Paris]-Centre National de la Recherche Scientifique (CNRS), Physico-Chimie-Curie (PCC), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut Curie [Paris]-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Analyse d'Images Quantitative, Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS), Imagerie Dynamique (Plate-Forme) (PFID), Institut Pasteur [Paris] (IP), Laboratoire de Biologie et Contrôle des Organismes Parasites, Université Paris-Sud - Paris 11 (UP11), Biologie cellulaire du parasitisme, Institut Pasteur [Paris] (IP)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre National de la Recherche Scientifique (CNRS)-Institut Curie [Paris]-Université Pierre et Marie Curie - Paris 6 (UPMC), Centre National de la Recherche Scientifique (CNRS)-Institut Curie [Paris]-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Chimie du CNRS (INC), Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS), Institut Pasteur [Paris], Institut Pasteur [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM) |
Jazyk: | angličtina |
Rok vydání: | 2005 |
Předmět: |
MESH: Myosin Type II
Movement Protozoan Proteins MESH: Cricetinae MESH: Movement MESH: Hepatocytes MESH: Lectins Cricetinae Lectins [SDV.BC.IC]Life Sciences [q-bio]/Cellular Biology/Cell Behavior [q-bio.CB] Animals Humans MESH: Microscopy Confocal MESH: Animals [SDV.BBM.BC]Life Sciences [q-bio]/Biochemistry Molecular Biology/Biochemistry [q-bio.BM] MESH: Protozoan Proteins Cells Cultured Myosin Type II Microscopy Confocal MESH: Humans Staining and Labeling Entamoeba histolytica Epithelial Cells MESH: Entamoeba histolytica MESH: Staining and Labeling MESH: Epithelial Cells Hepatocytes MESH: Caco-2 Cells Caco-2 Cells MESH: Cells Cultured |
Zdroj: | Cellular Microbiology Cellular Microbiology, 2005, 7 (1), pp.19-27. ⟨10.1111/j.1462-5822.2004.00426.x⟩ Cellular Microbiology, Wiley, 2005, 7 (1), pp.19-27. ⟨10.1111/j.1462-5822.2004.00426.x⟩ |
ISSN: | 1462-5814 1462-5822 |
DOI: | 10.1111/j.1462-5822.2004.00426.x⟩ |
Popis: | International audience; Entamoeba histolytica is the human parasite responsible of amoebiasis, during which highly motile trophozoites invade the intestinal epithelium leading to amoebic colitis, and disseminate via the blood circulation causing liver abscesses. The invasive process, central to the pathogenesis, is known to be driven by parasites motility. To investigate molecules responsible for in vivo motion, we performed a high resolution dynamic imaging analysis using two-photon laser scanning microscopy. Image analysis of the parasites during invasion of Caco-2 cell monolayers, an enterocyte-like model, and hamster liver shows that E. histolytica undergoes non-Brownian motion. However, studies of movements of parasite strains dominant negative for myosin II, a central component of the cytoskeleton, and for Gal-GalNAc lectin, a major adhesion molecule, indicate that myosin II is essential for E. histolytica intercellular motility through intestinal cell monolayers and for its motility in liver. In contrast, the Gal-GalNAc lectin exclusively triggers invasion of the liver. These observations are in agreement with emerging studies that highlight marked differences in the way that cells migrate in vitro in two dimensions versus in vivo in three dimensions. The approach that we have developed should be powerful to identify adhesive complexes required for in vivo cell migration in normal and pathogenic situations and may, thereby, lead to new therapeutic drug, for pathologies based on cell motility and adhesion. |
Databáze: | OpenAIRE |
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