4.3 Article

Involvement of ROS/ASMase/JNK signalling pathway in inhibiting UVA-induced apoptosis of HaGaT cells by polypeptide from Chlamys farreri

Journal

FREE RADICAL RESEARCH
Volume 42, Issue 1, Pages 12-19

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/10715760701762415

Keywords

polypeptide from Chlamys farreri; ultraviolet A; apoptosis; reactive oxygen species; acid sphingomyelinase; JNK

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Polypeptide from Chlamys farreri (PCF), a novel marine active material isolated from gonochoric Chinese scallop C. farreri, has potential antioxidant activity and protective effect against ultraviolet (UV) irradiation. The aim was to investigate whether PCF protects HaCaT cells from apoptosis induced by UVA and explore related molecular mechanisms. The results showed that PCF significantly prevented UVA-incluced apoptosis of HaCaT cells. PCF not only strongly reduced the intracellular reactive oxygen species (ROS) production, but also diminished expression of acid sphingomyelinase (ASMase) and phosphorylated JNK in HaCaT cells radiated by UVA in a dose-dependent manner. Pre-treatment with ROS scavenger NAC, ASMase inhibitor Desipramine or JNK inhibitor SP600125 was found to effectively prohibit UVA-induced apoptosis and Desipramine markedly blocked phosphorylation of JNK. So it is concluded that PCF obviously protects HaCaT cells from apoptosis induced by UVA and protective effects may attribute to decreasing intracellular ROS level and blocking ASMase/JNK apoptotic signalling pathway.

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