PUBLICATION

Fish Erythrocyte Extracellular Traps (FEETs) are an evolutionary conserved cellular process triggered by different stimuli

Authors
Rinaldi, G., Álvarez de Haro, N., Fernando, A.J., Desbois, A.P., Robb, C.T., Rossi, A.G.
ID
ZDB-PUB-230227-34
Date
2023
Source
Fish & shellfish immunology   136: 108638 (Journal)
Registered Authors
Rossi, Adriano
Keywords
Erythrocytes, Evolution, Extracellular DNA traps, FEETs, Immunity, Zebrafish
MeSH Terms
  • Animals
  • Erythrocytes/metabolism
  • Extracellular Traps*
  • Mammals
  • Zebrafish
PubMed
36842638 Full text @ Fish Shellfish Immunol.
Abstract
Fish erythrocytes remain nucleated, unlike mammalian erythrocytes that undergo enucleation during maturation. Besides oxygen transport, fish erythrocytes are capable of several immune defence processes and thus these cells are candidates for carrying out ETotic responses. ETosis is an evolutionary conserved innate immune defence process found in both vertebrates and invertebrates, which involves the extrusion of DNA studded with antimicrobial effector proteins into the extracellular space that traps and kills microorganisms. In this present report, we demonstrate that erythrocytes from Danio rerio (zebrafish) produce ETotic-like responses when exposed to both chemical and physiological inducers of ETosis. Furthermore, erythrocytes from Salmo salar (Atlantic salmon) behaved in a similar way. We have termed these ET-like formations, as Fish Erythrocyte Extracellular Traps (FEETs). Several inducers of mammalian NETosis, such as the protein kinase C (PKC) activator phorbol 12-myristate 13-acetate (PMA) and the calcium ionophore ionomycin, induced FEETs. Moreover, we found that FEETs depend on the activation of PKC and generation of mitochondrial reactive oxygen species (mROS). This present report is the first demonstration that fish erythrocytes can exhibit ETotic-like responses, unveiling a previously unknown function, which sheds new light on the innate immune arsenal of these cells.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping