Extracellular vesicles from the trematodes Fasciola hepatica and Dicrocoelium dendriticum trigger different responses in human THP‐1 macrophages

Author:

Sánchez‐López Christian M.12,González‐Arce Aránzazu1,Soler Carla23,Ramírez‐Toledo Víctor4,Trelis María12,Bernal Dolores5,Marcilla Antonio12

Affiliation:

1. Área de Parasitología, Departament de Farmacia i Tecnologia Farmacèutica i Parasitologia Universitat de València Burjassot (Valencia) Spain

2. Joint Research Unit on Endocrinology, Nutrition and Clinical Dietetics Health Research IIS La Fe‐Universitat de València Valencia Spain

3. Food & Health Lab. Instituto de Ciencia de los Materiales Parque Científico, Universitat de València Valencia Spain

4. Veterinari de Salut Pública Centre de Salut Pública de Manises Valencia Spain

5. Departament de Bioquímica i Biologia Molecular, Facultat de Ciències Biològiques Universitat de València Burjassot (Valencia) Spain

Abstract

AbstractExtracellular vesicles (EVs) released by the helminths Dicrocoelium dendriticum and Fasciola hepatica are important modulators of the host immune response, contributing to the establishment of the infection. Monocytes and, in particular, macrophages are major regulators of the inflammatory response and are likely responsible for the phagocytosis of most of the parasite EVs. In this study, we isolated EVs from F. hepatica (FhEVs) and D. dendriticum (DdEVs) by size exclusion chromatography (SEC) and characterized them by nanoparticle tracking analysis, transmission electron microscopy and LC‐MS/MS, and analyzed the cohort of proteins. The treatment of monocytes/macrophages with FhEVs, DdEVs or EV‐depleted fractions from SEC, demonstrated species‐specific effects of the EVs. In particular, FhEVs reduce the migratory capacity of monocytes and the analysis of the cytokine profile showed that they induce a mixed M1/M2 response, exerting anti‐inflammatory properties in Lipopolysaccharide‐activated macrophages. In contrast, DdEVs do not affect monocyte migration and seem to have pro‐inflammatory properties. These results correlate with the differences in the life cycle of both parasites, suggesting different host immune responses. Only F. hepatica migrates to the bile duct through the liver parenchyma, driving the host immune response to heal deep erosions. Furthermore, the proteomic analysis of the macrophages upon FhEV treatment identified several proteins that might be involved in FhEV‐macrophage interactions.

Funder

Agencia Estatal de Investigación

Generalitat Valenciana

Publisher

Wiley

Subject

Cell Biology,Histology

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