Broad early immune response of porcine epithelial jejunal IPI-2I cells to Entamoeba histolytica
Autor: | Sandrine Melo, François Meurens, Aurore Grave, Henri Salmon, Fabienne Girard-Misguich, Nancy Guillén |
---|---|
Přispěvatelé: | Infectiologie Animale et Santé Publique (UR IASP), Institut National de la Recherche Agronomique (INRA), Biologie Cellulaire du Parasitisme, Institut Pasteur [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM), Institut Pasteur [Paris] (IP)-Institut National de la Santé et de la Recherche Médicale (INSERM), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), This work was supported in part by the transversal research program INRA-Pasteur (PTR-291, 'Development of an immunopathologic swine model for intestin |
Jazyk: | angličtina |
Rok vydání: | 2009 |
Předmět: |
Chemokine
MESH: Dysentery Amebic MESH: Swine Diseases Phagocyte Swine NEUTROPHIL EPITHELIAL CELLS ENTAMOEBA HISTOLYTICA 0302 clinical medicine MESH: Up-Regulation MESH: Animals Intestinal Mucosa MESH: Swine Swine Diseases MESH: Cytokines 0303 health sciences biology Entamoeba histolytica Acquired immune system 3. Good health Up-Regulation medicine.anatomical_structure Jejunum MESH: Intestinal Mucosa Dysentery Amebic Cytokines [SDV.IMM]Life Sciences [q-bio]/Immunology MESH: Immunity Innate medicine.symptom Immunology Inflammation Microbiology Cell Line 03 medical and health sciences Immune system INNATE RESPONSE parasitic diseases medicine Animals Molecular Biology 030304 developmental biology PIG Innate immune system MESH: Entamoeba histolytica biology.organism_classification Immunity Innate MESH: Cell Line CCL20 MESH: Jejunum biology.protein 030215 immunology |
Zdroj: | Molecular Immunology Molecular Immunology, Elsevier, 2009, 46 (5), pp.927-936 Molecular Immunology, 2009, 46 (5), pp.927-936. ⟨10.1016/j.molimm.2008.09.036⟩ |
ISSN: | 0161-5890 |
DOI: | 10.1016/j.molimm.2008.09.036⟩ |
Popis: | International audience; Amoebiasis caused by Entamoeba histolytica triggers an acute inflammatory response at early stages of intestinal infection. The patho-physiological study of intestinal amoebiasis requires the development of powerful animal models. Swine provide robust model for human diseases and they could be used to study intestinal amoebiasis. Here, we introduce an in vitro model of swine intestinal epithelial cell (IPI-21) co-cultured with E. histolytica. Intestinal epithelial cells (IECs) have crucial roles in sensing pathogens and initiating innate immune response, which qualitatively influence adaptive immune response against them. The contact between the two cells induces marked macroscopic lesions of IEC monolayer and striking alteration of the IPI-21 cell phenotype including blebbing, such as loss of attachment before to be phagocyte by the trophozoite. Increase in Lactate Dehydrogenase (LDH) levels in the culture supernatant of IECs was observed when ameba is present and could reflect the cellular cytotoxicity exerted by the parasite. Using quantitative real-time PCR, we identified the up-regulation of cytokines/chemokines implicated in neutrophil chemoattraction and inflammation, such as CCL2, CCL20, CXCL2, CXCL3, GM-CSF, IL1 alpha, IL6 and IL8, in response to the parasite that can further regulate the immunoregulatory functions of the immune cells of the host. The study points a cardinal role of these pro-inflammatory compounds as central mediators in the interaction IECs/ameba and suggests mechanisms by which they coordinate intestinal immune response. This will focus future efforts on delineating the molecular and cellular mechanisms of other cell partners by the way of in vivo infection of swine. (C) 2008 Elsevier Ltd. All rights reserved. |
Databáze: | OpenAIRE |
Externí odkaz: |