TY - JOUR
T1 - Participation of ecto-5?-nucleotidase in the inflammatory response in an adult zebrafish (Danio rerio) model
AU - Nazario, Luiza Reali
AU - de Sousa, Jessica Streb
AU - Silveira, Francielle Schroeder de Moraes
AU - Costa, Kesiane Mayra
AU - de Oliveira, Giovanna Medeiros Tavares
AU - Bogo, Mauricio Reis
AU - da Silva, Rosane Souza
PY - 2022/10
Y1 - 2022/10
N2 - The ecto-5 '-nucleotidase is an important source of adenosine in the extracellular medium. Adenosine modulation appears early in evolution and performs several biological functions, including a role as an anti-inflammatory molecule. Here, we evaluate the activity and mRNA expression of ecto-5 '-nucleotidase in response to lipopolysaccharide (LPS) using zebrafish as a model. Adult zebrafish were injected with LPS (10 mu g/g). White blood cell differential counts, inflammatory markers, and ecto-5 '-nucleotidase activity and expression in the encephalon, kidney, heart, and intestine were evaluated at 2, 12, and 24 h post-injection (hpi). At 2 hpi of LPS, an increase in neutrophils and monocytes in peripheral blood was observed, which was accompanied by increased tnf-alpha expression in the heart, kidney, and encephalon, and increased cox-2 expression in the intestine and kidney. At 12 hpi, monocytes remained elevated in the peripheral blood, while tnf-alpha expression was also increased in the intestine. At 24 hpi, the white blood cell differential count no longer differed from that of the control, whereas tnf-alpha expression remained elevated in the encephalon but reduced in the kidney compared with the controls. AMP hydrolysis in LPS-treated animals was increased in the heart at 24 hpi [72 %; p = 0.029] without affecting ecto-5 '-nucleotidase gene expression. These data indicate that, in most tissues studied, inflammation does not affect ecto-5 '-nucleotidase activity, whereas in the heart, a delayed increase in ecto-5 '-nucleotidase activity could be related to tissue repair.
AB - The ecto-5 '-nucleotidase is an important source of adenosine in the extracellular medium. Adenosine modulation appears early in evolution and performs several biological functions, including a role as an anti-inflammatory molecule. Here, we evaluate the activity and mRNA expression of ecto-5 '-nucleotidase in response to lipopolysaccharide (LPS) using zebrafish as a model. Adult zebrafish were injected with LPS (10 mu g/g). White blood cell differential counts, inflammatory markers, and ecto-5 '-nucleotidase activity and expression in the encephalon, kidney, heart, and intestine were evaluated at 2, 12, and 24 h post-injection (hpi). At 2 hpi of LPS, an increase in neutrophils and monocytes in peripheral blood was observed, which was accompanied by increased tnf-alpha expression in the heart, kidney, and encephalon, and increased cox-2 expression in the intestine and kidney. At 12 hpi, monocytes remained elevated in the peripheral blood, while tnf-alpha expression was also increased in the intestine. At 24 hpi, the white blood cell differential count no longer differed from that of the control, whereas tnf-alpha expression remained elevated in the encephalon but reduced in the kidney compared with the controls. AMP hydrolysis in LPS-treated animals was increased in the heart at 24 hpi [72 %; p = 0.029] without affecting ecto-5 '-nucleotidase gene expression. These data indicate that, in most tissues studied, inflammation does not affect ecto-5 '-nucleotidase activity, whereas in the heart, a delayed increase in ecto-5 '-nucleotidase activity could be related to tissue repair.
KW - Adenosine
KW - CD75
KW - Endotoxin
KW - Lipopolysaccharide
KW - Purinergic system
KW - TOLL-LIKE RECEPTOR
KW - ADENOSINE RECEPTORS
KW - ONTOGENIC PROFILE
KW - BRAIN MEMBRANES
KW - EXPRESSION
KW - IDENTIFICATION
KW - SYSTEM
KW - ECTO-5'-NUCLEOTIDASE
KW - LIPOPOLYSACCHARIDE
KW - METABOLISM
U2 - 10.1016/j.cbpc.2022.109402
DO - 10.1016/j.cbpc.2022.109402
M3 - Article
SN - 1532-0456
VL - 260
JO - Comparative biochemistry and physiology c-Toxicology & pharmacology
JF - Comparative biochemistry and physiology c-Toxicology & pharmacology
M1 - 109402
ER -