<P>Polyunsaturated fatty acids usually undergo lipid peroxidation induced by reactive oxygen species (ROS). Calcium-independent cellular phospholipase A(2) (iPLA(2)) can maintain fatty acid compositions in phospholipids depending on physiologica...
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https://www.riss.kr/link?id=A107736872
2017
-
SCOPUS,SCIE
학술저널
48-56(9쪽)
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
<P>Polyunsaturated fatty acids usually undergo lipid peroxidation induced by reactive oxygen species (ROS). Calcium-independent cellular phospholipase A(2) (iPLA(2)) can maintain fatty acid compositions in phospholipids depending on physiologica...
<P>Polyunsaturated fatty acids usually undergo lipid peroxidation induced by reactive oxygen species (ROS). Calcium-independent cellular phospholipase A(2) (iPLA(2)) can maintain fatty acid compositions in phospholipids depending on physiological conditions. An insect iPLA(2) (Pi-iPLA(2)) was predicted from the transciptome of the Indianmeal moth, Plodia interpunctella. It encodes 835 amino acids. It possesses five ankyrin repeats in the N terminal and patatin lipase domain in the C terminal. Pi-iPLA(2) was expressed in all developmental stages of the Indianmeal moth. In the larval stage, it was expressed in all tissues tested. RNA interference (RNAi) specific to Pi-iPLA(2) was performed using specific double-stranded RNA (dsRNA). It resulted in almost 70% of reduction in gene expression. Under such RNAi condition, P. interpunctella exhibited significant accumulation of lipid per oxidation based on the amount of malondialdehyde. RNAi of Pi-PLA(2) expression also impaired cellular immune response of P. interpunctella. Chlorine dioxide (ClO2), an insecticidal agent by generating ROS, increased lipid peroxidation in a dose-dependent manner. However, the addition of vitamin E (an antioxidant) reduced the formation of lipid peroxidation. ClO2 treatment significantly reduced expression of Pi-iPLA(2) but increased lipid peroxidation in larval fat body of P. interpunctella. Furthermore, larvae treated with dsRNA specific to Pi-iPLA(2) were significantly susceptible to ClO2 treatment. These results suggest that Pi-iPLA(2) plays a crucial role in repairing damaged fatty acids from phospholipids. Our results also suggest that ClO2 can elevate lipid peroxidation through inhibiting Pi-iPLA(2) expression in addition to direct ROS production.</P>