Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Mais filtros

Base de dados
Ano de publicação
Tipo de documento
Intervalo de ano de publicação
1.
Fish Shellfish Immunol ; 72: 210-219, 2018 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-29108972

RESUMO

Vibrio parahemolyticus (V. parahemolyticus) is a major pathogen for abalone, an important economical shellfish in coastal area of China. There is little known about the abalone innate immune system against pathogen infection. Clip-domain serine proteases (cSPs) are increasingly recognized to play important roles in host immune defense in invertebrates. In this study, we cloned a cSP (Hdh-cSP) from abalone (Haliotis discus hannai). We found out that Hdh-cSP was widely expressed in multiple tissues of abalone, with highest level in the immune-like organ, hepatopancreas. V. parahemolyticus infection induced significantly elevated expression of Hdh-cSP in addition to better-characterized innate immune component genes including Rel/NF-κB, allograft inflammatory factor (ALInFa), macrophage expressed protein (MEP) and caspase-8. Importantly, the silencing of Hdh-cSP reduced the expression of these genes, suggesting that Hdh-cSP was an upstream regulatory factor in V. parahemolyticus infection. Further analysis showed that apoptosis of hemocytes was inhibited when the transcription of Hdh-cSP was knocked down, suggesting that Hdh-cSP participated in cell apoptosis by regulation of caspase 8 expression in V. parahemolyticus infection. Therefore, our study established an important role of cSP in the innate immunity against V. parahemolyticus infection in abalone.


Assuntos
Gastrópodes/genética , Gastrópodes/imunologia , Regulação da Expressão Gênica/imunologia , Imunidade Inata/genética , Serina Proteases/genética , Serina Proteases/imunologia , Sequência de Aminoácidos , Animais , Sequência de Bases , Clonagem Molecular , Gastrópodes/química , Gastrópodes/enzimologia , Perfilação da Expressão Gênica , Filogenia , Alinhamento de Sequência , Serina Proteases/química , Vibrio
SELEÇÃO DE REFERÊNCIAS
Detalhe da pesquisa