Abstract

Currently, inflammatory bowel disease (IBD) is a serious public health problem on the rise worldwide. In this work, we utilized the zebrafish to introduce a new model of intestinal inflammation triggered by food intake. Taking advantage of the translucency of the larvae and the availability of transgenic zebrafish lines with fluorescently labeled macrophages, neutrophils, or lymphocytes, we studied the behavior of these cell types in vivo during the course of inflammation. We established two feeding strategies, the first using fish that were not previously exposed to food (naïve strategy) and the second in which fish were initially exposed to normal food (developed strategy). In both strategies, we analyzed the effect of subsequent intake of a control or a soybean meal diet. Our results showed increased numbers of innate immune cells in the gut in both the naïve or developed protocols. Likewise, macrophages underwent drastic morphological changes after feeding, switching from a small and rounded contour to a larger and dendritic shape. Lymphocytes colonized the intestine as early as 5 days post fertilization and increased in numbers during the inflammatory process. Gene expression analysis indicated that lymphocytes present in the intestine correspond to T helper cells. Interestingly, control diet only induced a regulatory T cell profile in the developed model. On the contrary, soybean meal diet induced a Th17 response both in naïve and developed model. In addition, when feeding was performed in rag1-deficient fish, intestinal inflammation was not induced indicating that inflammation induced by soybean meal is T cell-dependent.

Highlights

  • Intestinal inflammation is a feature of several chronic pathologies such as inflammatory bowel disease (IBD) in humans as well as of similar pathologies in fish [1,2,3]

  • To analyze mucosal immune responses in intestines of fish exposed for first time to food, we used a well-established inflammation model [26], which consists of 4 days of feeding with soybean meal-based diet, from 5 to 9 dpf (Supplementary Figure 1A)

  • The understanding of biological processes associated with intestinal inflammatory diseases such IBD has historically been a very active research focus due to the high prevalence of these pathologies worldwide

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Summary

Introduction

Intestinal inflammation (or enteritis) is a feature of several chronic pathologies such as inflammatory bowel disease (IBD) in humans as well as of similar pathologies in fish [1,2,3]. Enteritis is characterized by a drastic increase of natural killer cells in the gut as well as activation of mast cells [7]. Each of these cell types secretes specific cytokines that trigger several pathways characteristic of enteritis [7]. CD4+ T helper (Th) cells are critical for proper immune cell homeostasis and Zebrafish T Cell-Dependent Intestinal Inflammation host defense but are major contributors to the pathology of autoimmune and inflammatory diseases [8]. Functional defects in Tregs underlie infectious, autoimmune and chronic inflammatory conditions, including IBD [11, 12]

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