The Interplay of TLR-NFκB Signalling Pathway and Functional Immune-Related Enzymes in the Inflammatory Response of Ciona robusta

Author:

Bisanti Luca12ORCID,La Corte Claudia12ORCID,Dara Mariano12ORCID,Bertini Federica12,Vizioli Jacopo3ORCID,Parisi Maria Giovanna12ORCID,Cammarata Matteo12ORCID,Parrinello Daniela12ORCID

Affiliation:

1. Marine Immunobiology Laboratory, Department of Earth and Marine Sciences, University of Palermo, 90128 Palermo, Italy

2. National Biodiversity Future Center (NBFC), 90133 Palermo, Italy

3. Laboratoire Protéomique, Réponse Inflammatoire et Spectrométrie de Masse (Inserm U1192), Département de Biologie, Université de Lille, F-59000 Lille, France

Abstract

The close phylogenetic relationship between ascidians (Tunicata) and vertebrates makes them a powerful model for studying the innate immune system. To better understand the nature and dynamics of immune responses and the mechanisms through which bacterial infections are detected and translated into inflammation in Ciona robusta, we applied an approach combining in vivo lipopolysaccharide (LPS) stimulation, immune-labelling techniques and functional enzymatic analyses. The immunohistochemistry showed that Toll-like receptor 4 (TLR4) and nuclear factor kappa B (NFκB) were expressed during the inflammatory pharynx response 4 h post-LPS, with the formation of nodules in pharynx vessel lumen. Also, the endothelium vessels were involved in the inflammatory response. Observations of histological sections from naive and buffer-inoculated ascidians confirmed an immuno-positive response. Enzyme immune parameters—which included the activity of phenoloxidase, glutathione peroxidase, lysozyme, alkaline phosphatase and esterase—showed up-modulation 4 h after LPS injection, confirming their participation during ascidian inflammatory response. These findings provide new insights into the mechanisms underlying the LPS-induced C. robusta response and suggest that a broad innate immune mechanism, as in vertebrates, is involved in the regulation of inflammatory responses. Further findings in this direction are needed to cover knowledge gaps regarding the organized set of molecular and cellular networks involved in universal immune interactions with pathogens.

Funder

Fund for University Research

National Biodiversity Future Center Project

Publisher

MDPI AG

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