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Molecular mechanisms of polypeptide from Chlamys farreri protecting HaCaT cells from apoptosis induced by UVA plus UVB

  
@article{APS4292,
	author = {Ming-qing Gao and Shen-bo Guo and Xue-hong Chen and Wei Du and Chun-bo Wang},
	title = {Molecular mechanisms of polypeptide from  Chlamys farreri  protecting HaCaT cells from apoptosis induced by UVA plus UVB},
	journal = {Acta Pharmacologica Sinica},
	volume = {28},
	number = {7},
	year = {2016},
	keywords = {},
	abstract = {Aim: To investigate the mechanism of polypeptide from Chlamys farreri (PCF) protecting HaCaT cells from apoptosis induced by UVA plus UVB in vitro.
Methods: An apoptotic model of UV irradiation-induced HaCaT cells was established. The 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide assay, agarose gel electrophoresis, biochemical methods, and Western blotting were employed in the study.
Results: PCF inhibited the UV irradiation-induced apoptosis of HaCaT cells. PCF strongly reduced the intracellular reactive oxygen species level, enhanced activities of superoxide dismutase and glutathione peroxidase and increased the total anti-oxidative capacity in HaCaT cells following UV irradiation. Furthermore, we found that PCF could inhibit the phosphorylation of c-Jun amino-terminal kinase and the activity of caspase-3 in a concentration-dependent manner.
Conclusion: PCF protected HaCaT cells from apoptosis induced by UVA plus UVB, mainly through decreasing the intracellular ROS level and increasing the activities of anti-oxidative enzymes to block the ROS-JNK-caspase-3-apoptosis signaling pathway},
	issn = {1745-7254},	url = {http://www.chinaphar.com/article/view/4292}
}