摘要
目的探讨DHA对神经生长因子NGF诱导PC12细胞的分化作用及其对BMP通路的影响。方法分别用100μg·L-1NGF和100μg·L-1NGF+10μmol·L-1DHA处理PC12细胞,并在3、6、9 d进行免疫荧光染色,观察细胞突起长度和突起数目的变化;气相色谱法分析3、6、9 d NGF+DHA组与NGF组PC12细胞的DHA含量;Western blot法检测NGF+DHA组与NGF组中BMP4、BMP7、BMPR-Ⅱ和pSmad 1/5/8蛋白的表达。结果 NGF+DHA处理组与NGF组相比,突起数目和突起长度明显增多和增长(P<0.01);胞内的DHA含量明显增加(P<0.01);BMP4、BMP7、BMPR-Ⅱ和p-Smad 1/5/8蛋白的表达升高(P<0.05)。结论 DHA能促进NGF诱导的PC12细胞分化,其机制可能与上调BMPs蛋白表达有关。
Aim To investigate the effect of DHA on NGF-induced neuronal differentiation of PC12 cells and explore the possible mechanism via regulating BMP pathway. Methods PC12 cells were treated with 100μg·L-1 NGF and 100 μg·L-1 NGF + 10 μmol· L-1 DHA for 3, 6 and 9 days respectively. The length and number of neurite were detected by immunofluores-cenc. DHA content was analyzed by gas chromatogra-phy in all groups. The protein expression of BMP4, BMP7 , BMPR-II and p-Smad 1/5/8 was determined by Western blot. Results The length of total primary neurite in NGF+DHA groups was obviously increased, longer than that in NGF group; DHA content in 10μmol · L-1 DHA group was higher than that in the control group;NGF+DHA groups also unregulated the protein expression of BMP4 , BMP7 , BMPR-II and p-Smad 1/5/8 . Conclusion DHA promotes NGF-in-duced neuronal differentiation in PC12 cells, which may be associated with the upregulation of BMP path-way protein.
出处
《中国药理学通报》
CAS
CSCD
北大核心
2014年第9期1247-1251,共5页
Chinese Pharmacological Bulletin
基金
国家自然科学基金资助项目(No 31272389)
广东省自然科学基金资助项目(No S2011010005597)