GnIH通过p38MAPK信号通路对猪卵巢颗粒细胞自噬与凋亡的影响
张鑫,霍孔林,宋星星,张多妮,胡文,胡传活(),李珣()
Effects of GnIH on Autophagy and Apoptosis of Porcine Ovarian Granulosa Cells via p38MAPK Signaling Pathway
Xin ZHANG,KongLin HUO,XingXing SONG,DuoNi ZHANG,Wen HU,ChuanHuo HU(),Xun LI()

图5. 用p38激活剂孵育,用不同剂量GnIH(0、10-6、10-8、10-10、10-12)处理pGCs,Western blot检测caspase-3、Bax和Bcl-2的免疫印迹及统计学分析
用ImageJ进行灰度值分析。数值为平均值±S.E,与对照组比较,星号表示显著差异。*P<0.05;**P<0.01

Fig. 5. After incubated with p38 activator, RFRP-3 concentration gradient (0, 10-6, 10-8, 10-10, 10-12) was treated with pGCs.Western blot caspase-3,Bax and Bcl-2 and statistical analysis (n=3)
Densitometric quantification was performed using ImageJ with GAPDH as the internal control for normalization. Values are mean±S.E. Compared with control group, asterisk indicates significant difference. *P<0.05; **P<0.01