PUBLICATION

Toll-like receptor adaptor protein TIRAP has specialized roles in signaling, metabolic control and leukocyte migration upon wounding in zebrafish larvae

Authors

Liu, L., Hu, W., Kerman, F.D., Spaink, H.P.

ID

ZDB-PUB-250109-219

Date

2025

Source

International journal of biological sciences 21: 823841823-841 (Journal)

Registered Authors

Spaink, Herman P.

Keywords

Mal, metabolome, neutrophil migration, tirap, tissue wounding, transcriptome

Datasets

GEO:GSE270453

MeSH Terms

Leukocytes/metabolism
Zebrafish Proteins*/genetics
Zebrafish Proteins*/metabolism
Cell Movement*
Animals
Signal Transduction*
Macrophages/metabolism
Neutrophils/metabolism
Myeloid Differentiation Factor 88/genetics
Myeloid Differentiation Factor 88/metabolism
Larva*/metabolism
Toll-Like Receptor 2/genetics
Toll-Like Receptor 2/metabolism
Zebrafish*
Receptors, Interleukin-1/genetics
Receptors, Interleukin-1/metabolism

(all 16)

PubMed

39781449 Full text @ Int. J. Biol. Sci.

Abstract

The TIRAP protein is an adaptor protein in TLR signaling which links TLR2 and TLR4 to the adaptor protein Myd88. The transcriptomic profiles of zebrafish larvae from a tirap, myd88 and tlr2 mutant and the corresponding wild type controls under unchallenged developmental conditions revealed a specific involvement of tirap in calcium homeostasis and myosin regulation. Metabolomic profiling showed that the tirap mutation results in lower glucose levels, whereas a tlr2 mutation leads to higher glucose levels. A tail-wounding zebrafish larval model was used to identify the role of tirap in leukocyte migration to tissue wounding. We found that more neutrophils were recruited to the wounded region in the tirap mutant larvae compared to the wild type controls, whereas there was no difference in macrophage recruitment. In contrast, published data show that tlr2 and myd88 mutants recruit fewer neutrophils and macrophages to the wounds. Based on cell tracking analysis, we demonstrate that the neutrophil migration speed is increased in the tirap mutant in contrast to neutrophil behavior in myd88 and tlr2 mutants. In conclusion, we show that tirap plays specialized roles distinct from tlr2 and myd88 in signaling, metabolic control, and in regulating neutrophil migration speed upon wounding.

Genes / Markers

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