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Published on: November 4, 2016
Nematode microRNAs can Individually Regulate Interferon Regulatory Factor 4 and mTOR in Differentiating T Helper 2
Julien Soichot1, Nathalie Guttmann1, Hubert Rehrauer2
1Institute of Parasitology, Vetsuisse Faculty, University of Zurich, Zurich, Switzerland.
Abstract:
Parasitic nematodes are masterful immunomodulators. This class of pathogens has evolved a spectrum of sophisticated strategies to regulate and evade host immune responses, mediated through the release of various molecules. In this context, the release of microRNAs (miRNAs), short post-transcriptional regulators of gene expression, has been of particular interest in the host-parasite interplay. Evidence that parasite-derived miRNAs modulate host innate and adaptive immune responses has become increasingly compelling. However, since miRNAs are usually contained in extracellular vesicles containing other mediators, it is difficult to assign an observed effect on host cells to miRNAs specifically. Here, the effects of some abundantly secreted miRNAs by nematodes used as models of gastrointestinal infections (Heligmosomoides polygyrus bakeri, Trichuris muris and Ascaris suum) were evaluated, addressing the potential of parasite miRNAs to impair in vitro differentiation of two important types of immune cells in the context of helminth infections, Th2 lymphocytes and macrophages. Mimicking a continuous exposure to low concentrations of nematode miRNAs, the interferon gamma signaling, the IL-2/STAT5 signaling, and the mTOR signaling pathways were identified as downregulated by Hpo-miR-71-5p. Interferon regulatory factor 4 (Irf4) was validated as a target of Hpo-miR-71-5p, while Mtor is targeted by Asu-miR-791-3p, abundant in the T. muris secretions. By trend, Hpo-miR-71-5p impacts mildly but consistently on the amounts of inflammatory cytokines in unpolarized macrophages but leads to slightly increased IL-10 level in alternatively activated cells. In addition, our data suggests that transfected miRNAs remain for days in recipient cells, and that Hpo-miR-71-5p can incorporate into mouse Argonaute protein complexes. Nematode miRNAs can impair both innate and adaptive arms of host immunity. Hpo-miR-71-5p in particular, absent in mammals, interacts with host genes and pathways with crucial involvement in anthelmintic immune responses. This report brings new insights into the dynamics of miRNA-driven immunomodulation and highlights putative targeted pathways. Although the absolute repression is subtle, it is expected that the dozens of different miRNAs released by nematodes may have a synergistic effect on surrounding host cells.
Insights
Nematode-secreted microRNAs (miRNAs) can suppress host immune cell differentiation and function. Specific parasite miRNAs, like Hpo-miR-71-5p, target key immune pathways, potentially impairing the host response to parasitic infections.
Area of Science:
- Immunology
- Molecular Biology
- Parasitology
Background:
- Parasitic nematodes employ sophisticated immune evasion strategies, including the release of molecules like microRNAs (miRNAs).
- Parasite-derived miRNAs are implicated in modulating host immune responses, but isolating their specific effects is challenging.
- Understanding how nematode miRNAs impact host immunity is crucial for developing new therapeutic strategies against helminth infections.
Purpose of the Study:
- To investigate the effects of nematode-secreted miRNAs on the in vitro differentiation of Th2 lymphocytes and macrophages.
- To identify specific nematode miRNAs and their host targets involved in immune modulation.
- To assess the potential of parasite miRNAs to impair host innate and adaptive immunity.
Main Methods:
- Exposure of immune cells to nematode-derived miRNAs from models of gastrointestinal infections (Heligmosomoides polygyrus bakeri, Trichuris muris, Ascaris suum).
- Analysis of signaling pathways (e.g., interferon gamma, IL-2/STAT5, mTOR) and gene targets (e.g., Irf4, Mtor) affected by specific miRNAs.
- Assessment of cytokine levels in macrophages and incorporation of miRNAs into host protein complexes.
Main Results:
- Hpo-miR-71-5p downregulated interferon gamma, IL-2/STAT5, and mTOR signaling pathways.
- Interferon regulatory factor 4 (Irf4) was validated as a target of Hpo-miR-71-5p, and Mtor as a target of Asu-miR-791-3p.
- Nematode miRNAs were shown to persist in host cells and can be incorporated into Argonaute complexes, suggesting functional integration.
Conclusions:
- Nematode-derived miRNAs can impair both innate and adaptive immune responses.
- Hpo-miR-71-5p, a non-mammalian miRNA, interacts with host pathways critical for anthelmintic immunity.
- The subtle but synergistic effects of multiple nematode miRNAs highlight a significant mechanism of host immune modulation by parasites.
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