Title of article :
Effects of RNA interference-mediated knock-down of hypoxia-inducible factor-α on respiratory burst activity of the Pacific oyster Crassostrea gigas hemocytes
Author/Authors :
Choi، نويسنده , , Seung Hyuk and Jee، نويسنده , , Bo Young and Lee، نويسنده , , Su Jin and Cho، نويسنده , , Mi Young and Lee، نويسنده , , Soon Jeong and Kim، نويسنده , , Jin-Woo and Jeong، نويسنده , , Hyun Do and Kim، نويسنده , , Ki Hong، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2013
Pages :
4
From page :
476
To page :
479
Abstract :
In mammals, hypoxia-inducible factor-1 α (HIF-1α) is known to play important roles not only in oxygen homeostasis but also in innate immune responses. In this study, to assess the functional role of HIF-α in respiratory burst activity of Crassostrea gigas hemocytes, oysters were injected with HIF-α- or green fluorescent protein (GFP)-targeted-long double-stranded RNAs (dsRNAs), and at 1, 3, and 7 days post-injection, knock-down of C. gigas HIF-α expression and production of reactive oxygen species (ROS) were analyzed. Expression of HIF-α in mantle, gill, and hemocytes of C. gigas was clearly down-regulated by injection of the HIF-α-targeted-long dsRNA, but was not inhibited by the GFP-targeted-long dsRNA, indicating that HIF-α expression was suppressed through sequence-specific and systemic RNA interference (RNAi). Respiratory burst activity of hemocytes was significantly increased by administration of GFP-targeted-long dsRNA. However, knock-down of HIF-α expression led to significant decrease of chemiluminescence (CL) response of C. gigas hemocytes at 3 and 7 days post-administration of HIF-α-targeted-long dsRNA, indicating the critical role of HIF-α in activation of respiratory burst activity of oyster hemocytes.
Keywords :
Knock-down of HIF-? , Respiratory burst activity , Hypoxia-inducible factor-? , Crassostrea gigas , RNA interference
Journal title :
Fish and Shellfish Immunology
Serial Year :
2013
Journal title :
Fish and Shellfish Immunology
Record number :
2112392
Link To Document :
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