» Articles » PMID: 31001250

Soybean Meal-Induced Intestinal Inflammation in Zebrafish Is T Cell-Dependent and Has a Th17 Cytokine Profile

Overview
Journal Front Immunol
Date 2019 Apr 20
PMID 31001250
Citations 28
Authors
Affiliations
Soon will be listed here.
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 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 -deficient fish, intestinal inflammation was not induced indicating that inflammation induced by soybean meal is T cell-dependent.

Citing Articles

Identification of Single-Nucleotide Polymorphisms in Differentially Expressed Genes Favoring Soybean Meal Tolerance in Higher-Growth Zebrafish (Danio rerio).

Ulloa P, Jilberto F, Lam N, Rincon G, Valenzuela L, Cordova-Alarcon V Mar Biotechnol (NY). 2024; 26(4):754-765.

PMID: 38958822 DOI: 10.1007/s10126-024-10343-7.


A review on current advancement in zebrafish models to study chronic inflammatory diseases and their therapeutic targets.

Balde A, Ramya C, Nazeer R Heliyon. 2024; 10(11):e31862.

PMID: 38867970 PMC: 11167310. DOI: 10.1016/j.heliyon.2024.e31862.


Isolation of Intestinal Macrophage Subpopulations for High-Quality Total RNA Purification in Zebrafish.

Del Rio-Jay Y, Barthelaix A, Reyes-Martinez C, Duperray C, Solis-Cascante C, Hidalgo Y Methods Protoc. 2024; 7(3).

PMID: 38804337 PMC: 11130952. DOI: 10.3390/mps7030043.


Maturation of the medaka immune system depends on reciprocal interactions between the microbiota and the intestinal tract.

Sakaguchi H, Sato Y, Matsumoto R, Gomikawa J, Yoshida N, Suzuki T Front Immunol. 2023; 14:1259519.

PMID: 37767090 PMC: 10520778. DOI: 10.3389/fimmu.2023.1259519.


Small fish, big discoveries: zebrafish shed light on microbial biomarkers for neuro-immune-cardiovascular health.

Sree Kumar H, Wisner A, Refsnider J, Martyniuk C, Zubcevic J Front Physiol. 2023; 14:1186645.

PMID: 37324381 PMC: 10267477. DOI: 10.3389/fphys.2023.1186645.


References
1.
Geissmann F, Jung S, Littman D . Blood monocytes consist of two principal subsets with distinct migratory properties. Immunity. 2003; 19(1):71-82. DOI: 10.1016/s1074-7613(03)00174-2. View

2.
Bouma G, Strober W . The immunological and genetic basis of inflammatory bowel disease. Nat Rev Immunol. 2003; 3(7):521-33. DOI: 10.1038/nri1132. View

3.
Rawls J, Samuel B, Gordon J . Gnotobiotic zebrafish reveal evolutionarily conserved responses to the gut microbiota. Proc Natl Acad Sci U S A. 2004; 101(13):4596-601. PMC: 384792. DOI: 10.1073/pnas.0400706101. View

4.
Langenau D, Ferrando A, Traver D, Kutok J, Hezel J, Kanki J . In vivo tracking of T cell development, ablation, and engraftment in transgenic zebrafish. Proc Natl Acad Sci U S A. 2004; 101(19):7369-74. PMC: 409925. DOI: 10.1073/pnas.0402248101. View

5.
Yoder J . Investigating the morphology, function and genetics of cytotoxic cells in bony fish. Comp Biochem Physiol C Toxicol Pharmacol. 2004; 138(3):271-80. DOI: 10.1016/j.cca.2004.03.008. View